SDS Table of Contents Click the desired link below to jump directly to that section in the SDS. STI(R*) SAFETY DATA SHEET PREPARED TO U.S. OSHA, CMA, ANSI, CANADIAN WHMIS, THE KOREAN ISHA (NOTICE 2009-68), THE JAPANESE INDUSTRIAL STANDARD JIS Z 7250:2000, MEXICAN NOM018-STPS 2000, SPRING SINGAPORE, AND THE GLOBAL HARMONIZATION STANDARD
AND OF THE COMPANY UNDERTAKING IDENTIFICATION OF THE MIXTURE: TRADE/MATERIAL NAME: STI MARINE FIRESTOP PUTTY (MPU) RELEVANT USE OF THE SUBSTANCE: FIRESTOP AND SOUND TRANSMISSION USES ADVISED AGAINST: NONE SUPPLIER/MANUFACTURER'S NAME (USA/CANADA): STI MARINE: A DIVISION OF SPECIFIED TECHNOLOGIES, INC. ADDRESS: 210 EVANS WAY, SOMERVILLE, NEW JERSEY 08876 BUSINESS PHONE: (908) 526-8000 (8:00AM TO 5:00PM EASTERN STANDARD TIME) EMERGENCY PHONE: U.S., CANADA: 1-800-255-3924 (24 HRS) INTERNATIONAL: +1-813-248-0585 (COLLECT-24 HRS) SUPPLIER/IMPORTER'S NAME (ASIA): ADDRESS: BUSINESS PHONE: EMAIL OF COMPETENT PERSON FOR INFORMATION ON SDS: TECHSERV@STIMARINE.COM NOTE: ALL UNITED STATES OCCUPATIONAL SAFETY AND HEALTH ADMINISTRATION STANDARD (29 CFR 1910.1200), U.S. STATE EQUIVALENT STANDARDS, CANADIAN WHMIS [CONTROLLED PRODUCTS REGULATIONS], MEXICAN NOM018-STPS 2000, SPRING SINGAPORE, AND JAPANESE JIS Z7250 REQUIRED INFORMATION IS INCLUDED IN APPROPRIATE SECTIONS BASED ON THE U.S. ANSI Z400.1-2010 FORMAT. THIS PRODUCT HAS BEEN CLASSIFIED IN ACCORDANCE WITH THE HAZARD CRITERIA OF THE COUNTRIES LISTED ABOVE.
GLOBAL HARMONIZATION AND JAPANESE JIS Z7253 LABELING AND CLASSIFICATION: THIS PRODUCT HAS BEEN CLASSIFIED PER UN GHS STANDARDS UNDER U.S., JAPANESE AND OTHER APPLICABLE REGULATIONS THAT REQUIRE GLOBAL HARMONIZATION COMPLIANCE. CLASSIFICATION: CARCINOGENIC CATEGORY 2, GERM CELL MUTAGEN CATEGORY 2, ACUTE DERMAL TOXICITY CATEGORY 5, EYE IRRITATION CATEGORY 2A, SKIN IRRITATION CATEGORY 2, SKIN SENSITIZATION CATEGORY 1, SPECIFIC TARGET ORGAN TOXICITY REPEATED EXPOSURE CATEGORY 2 SIGNAL WORD: WARNING HAZARD STATEMENTS: H351: SUSPECTED OF CAUSING CANCER. H341: SUSPECTED OF CAUSING GENETIC EFFECTS. H313: MAY BE HARMFUL IN CONTACT WITH SKIN. H315: CAUSES SKIN IRRITATION. H317: MAY CAUSE AN ALLERGIC SKIN REACTION. H319: CAUSES SERIOUS EYE IRRITATION. H373: MAY CAUSE DAMAGE TO ORGANS THROUGH PROLONGED OR REPEATED EXPOSURE. PRECAUTIONARY STATEMENTS: PREVENTION: P201: OBTAIN SPECIAL INSTRUCTIONS BEFORE USE. P202: DO NOT HANDLE UNTIL ALL SAFETY PRECAUTIONS HAVE BEEN READ AND UNDERSTOOD. P260: DO NOT BREATHE VAPORS/FUME. P271: USE ONLY OUTDOORS OR IN A WELL-VENTILATED AREA. P272: CONTAMINATED WORK CLOTHING SHOULD NOT BE ALLOWED OUT OF THE WORKPLACE. P280: WEAR PROTECTIVE GLOVES, CLOTHING, EYE PROTECTION AND FACE PROTECTION. RESPONSE: P308 + P313: IF EXPOSED OR CONCERNED: GET MEDICAL ADVICE/ATTENTION. P305 + P351 + P338: IF IN EYES: RINSE CAUTIOUSLY WITH WATER FOR SEVERAL MINUTES. REMOVE CONTACT LENSES, IF PRESENT AND EASY TO DO. P337 + P313: IF EYE IRRITATION PERSISTS: GET MEDICAL ADVICE/ATTENTION. P302 + P352: IF ON SKIN: WASH WITH PLENTY OF SOAP AND WATER. P333 + P313: IF SKIN IRRITATION OR RASH OCCURS: GET MEDICAL ADVICE/ATTENTION. P312: CALL A POISON CENTER OR DOCTOR IF YOU FEEL UNWELL. P362 + P364: TAKE OFF CONTAMINATED CLOTHING AND WASH IT BEFORE REUSE. P321: SPECIFIC TREATMENT (REMOVE FROM EXPOSURE AND TREAT SYMPTOMS). STORAGE: P403 + P233 + P405: STORE IN A WELL-VENTILATED PLACE. KEEP CONTAINER TIGHTLY CLOSED. STORE LOCKED UP. DISPOSAL: P501: DISPOSE OF CONTENTS/CONTAINERS IN ACCORDANCE WITH ALL LOCAL, REGIONAL, NATIONAL AND INTERNATIONAL REGULATIONS. HAZARD SYMBOLS: GHS07: EXCLAMATION MARK GHS08: HEALTH HAZARD KOREAN ISHA (NOTICE 2009-68) LABELING AND CLASSIFICATION: CLASSIFIED IN ACCORDANCE WITH ISHA NOTICE 2009-68. UNDER ISHA, NO DIFFERENCES IN CLASSIFICATION ARE APPLICABLE.
LABEL ELEMENTS CHEMICAL NAME CAS # WT% ALUMINUM TRIHYDRATE 21645-51-2 50-60% PROPRIETARY POLYMER 20-30% FORMALDEHYDE POLYMER WITH 35297-54-2 10-15% AMMONIA AND PHENOL PHENOL 108-95-2 1-3% SULFURIC ACID COMPOUND 12777-87-6 2-5% WITH GRAPHITE CRYSTALLINE SILICA 14808-60-7 TRACE FORMALDEHYDE 50-00-0 TRACE WATER AND OTHER TRACE BALANCE INGREDIENTS CHEMICAL CHINESE JAPANESE KOREAN TAIWAN LABEL ELEMENTS NAME IECSC ENCS # ECL # NESCI GHS & JAPANESE INVENTORY ECS JIS Z7253 CLASSIFICATION KOREAN ISHA CLASSIFICATION GHS HAZARD CODES ALUMINUM LISTED 1-17 KE-00980 LISTED SELF TRIHYDRATE CLASSIFICATION GHS & JAPANESE JIS Z7253, KOREAN ISHA: CLASSIFICATION: EYE IRRITATION CAT. 2A HAZARD CODES: H319 PROPRIETARY LISTED PROPRIETARY PROPRIETARY LISTED CLASSIFICATION POLYMER NOT APPLICABLE FORMAL- LISTED NOT LISTED KE-17082 LISTED SELF DEHYDE CLASSIFICATION POLYMER GHS & JAPANESE WITH JIS Z7253, AMMONIA KOREAN ISHA: AND CLASSIFICATION: PHENOL ACUTE ORAL TOXICITY CAT. 5, SKIN SENSITIZATION CAT. 1B, STOT RE CAT. 3 HAZARD CODES: H303, H317, H373 PHENOL LISTED 3-381 KE-28209 LISTED GHS & JAPANESE JIS Z7253, KOREAN ISHA: CLASSIFICATION: MUTAGENIC CAT. 2, ACUTE ORAL TOXICITY CAT. 3, ACUTE DERMAL TOXICITY CAT. 3, ACUTE INHALATION TOXICITY CAT. 3, SKIN CORROSION CAT. 1B, STOT RE CAT. 2 HAZARD CODES: H341, H301 + H311 + H331, H314, H373 SULFURIC NOT NOT KE-32585 LISTED SELF ACID LISTED LISTED CLASSIFICATION: COMPOUND GHS & JAPANESE WITH JIS Z7253, GRAPHITE KOREAN ISHA: CLASSIFICATION: CARCINOGENIC CAT. 2 HAZARD CODES: H351I CRYSTALLINE LISTED 1-548 KE-29983 LISTED SELF SILICA CLASSIFICATION: GHS & JAPANESE JIS Z7253, KOREAN ISHA: CLASSIFICATION: CARCINOGENIC CAT. 1, STOT (INHALATION- LUNGS) RE CAT. 2 HAZARD STATEMENT CODES: H350, H373 FORMAL- LISTED 2-482 KE-17074 LISTED GHS & JAPANESE DEHYDE JIS Z7253, KOREAN ISHA: CLASSIFICATION: CARCINOGENIC CAT. 2, ACUTE ORAL TOXICITY CAT. 3, ACUTE DERMAL TOXICITY CAT. 3, ACUTE INHALATION TOXICITY CAT. 3, SKIN CORROSION CAT. 1B, SKIN SENSITIZATION CAT. 1 HAZARD CODES: H351, H301 + H311 + H331, H314, H317 WATER AND CLASSIFICATION: OTHER NOT APPLICABLE TRACE INGREDIENTS SEE SECTION 16 FOR FULL TEXT OF CLASSIFICATION
DESCRIPTION OF FIRST AID MEASURES: SKIN EXPOSURE: IF ADVERSE SKIN EFFECTS OCCUR, DISCONTINUE USE AND FLUSH CONTAMINATED AREA. SEEK MEDICAL ATTENTION IF ADVERSE EFFECT OCCURS AFTER FLUSHING. INHALATION: IF FUMES OR VAPORS ARE INHALED, REMOVE VICTIM TO FRESH AIR. SEEK MEDICAL ATTENTION IF ADVERSE EFFECT CONTINUES AFTER REMOVAL TO FRESH AIR. EYE EXPOSURE: IF THIS PRODUCT CONTAMINATES THE EYES, RINSE EYES UNDER GENTLY RUNNING WATER. REMOVE CONTACT LENSES IF EASY TO DO. USE SUFFICIENT FORCE TO OPEN EYELIDS AND THEN "ROLL" EYES WHILE FLUSHING. MINIMUM FLUSHING IS FOR 20 MINUTES. THE CONTAMINATED INDIVIDUAL MUST SEEK MEDICAL ATTENTION IF ANY ADVERSE EFFECT CONTINUES AFTER RINSING. INGESTION: IF THIS PRODUCT IS SWALLOWED, CALL PHYSICIAN OR POISON CONTROL CENTER FOR MOST CURRENT INFORMATION. IF PROFESSIONAL ADVICE IS NOT AVAILABLE, DO NOT INDUCE VOMITING. NEVER INDUCE VOMITING OR GIVE DILUENTS (MILK OR WATER) TO SOMEONE WHO IS UNCONSCIOUS, HAVING CONVULSIONS, OR UNABLE TO SWALLOW. IF VICTIM IS CONVULSING, MAINTAIN AN OPEN AIRWAY AND OBTAIN IMMEDIATE MEDICAL ATTENTION. MEDICAL CONDITIONS AGGRAVATED BY EXPOSURE: SEE SECTION 11. INDICATION OF IMMEDIATE MEDICAL ATTENTION AND SPECIAL TREATMENT IF NEEDED: TREAT SYMPTOMS AND ELIMINATE EXPOSURE.
NFPA RATING: HEALTH 2 FLAMMABILITY 0 INSTABILITY 0 OTHER HAZARD SCALE: 0 = MINIMAL 1 = SLIGHT 2 = MODERATE 3 = SERIOUS 4 = SEVERE FLASH POINT: NOT DETERMINED. AUTOIGNITION TEMPERATURE: NOT AVAILABLE. FLAMMABLE LIMITS (IN AIR BY VOLUME, %): NOT APPLICABLE. FIRE EXTINGUISHING MEDIA: USE EXTINGUISHING MATERIALS SUITABLE FOR THE SURROUNDING AREA. UNSUITABLE FIRE EXTINGUISHING MEDIA: NONE KNOWN. UNUSUAL FIRE AND EXPLOSION HAZARDS: THIS PRODUCT IS FORMULATED TO BE NON-FLAMMABLE AND NON-COMBUSTIBLE. WHEN INVOLVED IN A FIRE, THIS MATERIAL MAY DECOMPOSE AND PRODUCE IRRITATING VAPORS AND TOXIC GASES EXPLOSION SENSITIVITY TO MECHANICAL IMPACT: NOT SENSITIVE. EXPLOSION SENSITIVITY TO STATIC DISCHARGE: NOT SENSITIVE. SPECIAL PROTECTIVE ACTIONS FOR FIRE-FIGHTERS: NO SPECIAL PROTECTIVE ACTIONS FOR FIRE-FIGHTERS ARE ANTICIPATED.
PERSONAL PRECAUTIONS AND EMERGENCY PROCEDURES: UNCONTROLLED RELEASES SHOULD BE RESPONDED TO BY TRAINED PERSONNEL USING PRE-PLANNED PROCEDURES. PROPER PROTECTIVE EQUIPMENT SHOULD BE USED. CALL CHEMTREC (1800-424-9300) FOR EMERGENCY ASSISTANCE. OR IF IN CANADA, CALL CANUTEC (613-996-6666). PERSONAL PROTECTIVE EQUIPMENT: PROPER PROTECTIVE EQUIPMENT SHOULD BE USED. SMALL SPILLS: WEAR RUBBER GLOVES. LARGE SPILLS: MINIMUM PERSONAL PROTECTIVE EQUIPMENT SHOULD BE RUBBER GLOVES, RUBBER BOOTS, FACE SHIELD. METHODS FOR CLEAN-UP AND CONTAINMENT: SPILLS OF THIS PRODUCT PRESENT MINIMAL HAZARD. SMALL SPILLS: SMALL RELEASES CAN BE CAREFULLY SWEPT UP OR CLEANED UP USING A DAMP SPONGE OR POLYPADS. LARGE SPILLS: ACCESS TO THE SPILL AREA SHOULD BE RESTRICTED. FOR LARGE SPILLS, DIKE OR OTHERWISE CONTAIN SPILL AND SWEEP-UP OR VACUUM WITH NON-SPARKING VACUUM. ALL SPILLS: PLACE ALL SPILL RESIDUE IN A DOUBLE PLASTIC BAG OR OTHER CONTAINMENT AND SEAL. CLOSE OFF SEWERS AND TAKE OTHER MEASURES TO PROTECT HUMAN HEALTH AND THE ENVIRONMENT AS NECESSARY. RINSE AREA WITH SOAP AND WATER SOLUTION AND FOLLOW WITH A WATER RINSE. ENVIRONMENTAL PRECAUTIONS: AVOID RELEASE TO THE ENVIRONMENT.
PRECAUTIONS FOR SAFE HANDLING: AS WITH ALL CHEMICALS, AVOID GETTING THIS MATERIAL ON YOU OR IN YOU. DO NOT EAT, DRINK, SMOKE, OR APPLY COSMETICS WHILE HANDLING THIS PRODUCT. WASH HANDS THOROUGHLY AFTER HANDLING THIS PRODUCT OR CONTAINERS OF THIS PRODUCT. AVOID BREATHING FUMES OR VAPORS. USE IN A WELL-VENTILATED LOCATION. CONDITIONS FOR SAFE STORAGE: STORE CONTAINERS IN A COOL, DRY LOCATION, AWAY FROM DIRECT SUNLIGHT, SOURCES OF INTENSE HEAT. SPECIFIC END USE(S): THIS PRODUCT IS FOR USE AS A SEALANT. FOLLOW ALL INDUSTRY STANDARDS FOR USE OF THIS PRODUCT. PROTECTIVE PRACTICES DURING MAINTENANCE OF CONTAMINATED EQUIPMENT: FOLLOW PRACTICES INDICATED IN SECTION 6 (ACCIDENTAL RELEASE MEASURES). MAKE CERTAIN THAT APPLICATION EQUIPMENT IS LOCKED AND TAGGED-OUT SAFELY, IF NECESSARY. COLLECT ALL RINSATES AND DISPOSE OF ACCORDING TO APPLICABLE FEDERAL, STATE, AND LOCAL PROCEDURES.
EXPOSURE LIMITS/CONTROL PARAMETERS: VENTILATION AND ENGINEERING CONTROLS: USE WITH ADEQUATE VENTILATION TO ENSURE EXPOSURE LEVELS ARE MAINTAINED BELOW THE LIMITS PROVIDED BELOW (IF APPLICABLE). EXHAUST DIRECTLY TO THE OUTSIDE, TAKING NECESSARY PRECAUTIONS FOR ENVIRONMENTAL PROTECTION. WORKPLACE EXPOSURE LIMITS/CONTROL PARAMETERS: CHEMICAL NAME CAS # EXPOSURE LIMITS IN AIR ACGIH-TLVS OSHA-PELS TWA STEL TWA STEL MG/M3 MG/M3 MG/M3 MG/M3 ALUMINUM TRIHYDRATE 21645-51-2 NE NE NE NE CRYSTALLINE SILICA 14808-60-7 0.025 NE 30 MG/M3 (TOTAL (QUARTZ) (RESP. DUST) / % SO2 + 2 FRACT.) 0.1 (VACATED 1989 PEL) 250 MPPCF (RESP. DUST) / % SiO2 + 5 OR 10 MG/M3 (RESP. DUST) / 0.2 % SO2 + 2 FORMALDEHYDE 50-00-0 SEN 0.37 0.75 PPM 2 PPM (CEILING) SEE 20 CFR NIC: D-SEN, RSEN 1910.1048(C) FORMALDEHYDE 35297-54-2 NE NE NE NE POLYMER WITH AMMONIA AND PHENOL PHENOL 108-95-2 19 (SKIN) SKIN 19 (SKIN) SKIN PROPRIETARY POLYMER NE NE NE NE SULFURIC ACID 12777-87-6 NE NE NE NE COMPOUND WITH GRAPHITE CHEMICAL NAME EXPOSURE LIMITS IN AIR NIOSH-RELS NIOSH OTHER TWA STEL IDLH MG/M3 MG/M3 MG/M3 MG/M3 ALUMINUM TRIHYDRATE NE NE NE DFG MAKS: TWA: 4 MG/M3 (INHALABLE FRACTION) 1.5 MG/M3 (RESPIRABLE FRACTION) DFG MAK PREGNANCY RISK CLASSIFICATION: D CRYSTALLINE SILICA 0.05 NE 50, Ca CARCINOGEN: (QUARTZ) (RESP. IARC-1, MAK-1 DUST) (RESPIRABLE FRACTION), NOSH-CA, NTP-K (RESPIRABLE FRACTION), TLV-A2 FORMALDEHYDE 0.016 PPM 0.1 PPM, 20 PPM DFG MAKS: 15 MIN. (Ca) TWA: 0.37 SEE POCKET GUIDE PEAK: APP. A 2xMAK 15-MIN AVERAGE VALUE, 1-HR INTERVAL, 4 PER SHIFT 1 (CEILING) DANGER OF SENSITIZATION OF THE SKIN DFG MAK GERM CELL MUTAGEN CATEGORY: 5 DFG MAK PREGNANCY RISK CLASSIFICATION: C CARCINOGEN: EPA-B1, IARC-1, MAK-4, NIOSH-CA, NTP-K, OSHA-CA, TLV-A2 FORMALDEHYDE NE NE NE NE POLYMER WITH AMMONIA AND PHENOL PHENOL 19 (SKIN) 60 (SKIN) 25 PPM DFG MAK: SKIN 15 MIN. CARCINOGEN: EPA-I, EPA-D, IARC-3, MAK-3B, TLV-A4 PROPRIETARY POLYMER NE NE NE NE SULFURIC ACID NE NE NE NE COMPOUND WITH GRAPHITE NE: NOT ESTABLISHED. CA: CARCINOGEN NIC: NOTICE OF INTENDED CHANGE DSEN: MAY CAUSE DERMAL SENSITIZATION. THIS NOTATION IS USED TO INDICATE THE POTENTIAL FOR DERMAL SENSITIZATION RESULTING FROM THE INTERACTION OF AN ABSORBED AGENT AND ULTRAVIOLET LIGHT (I.E. PHOTOSENSITIZATION) RSEN: MAY CAUSE RESPIRATORY SENSITIZATION SEN: CONFIRMED POTENTIAL WORKER SENSITIZATION AS A RESULT OF DERMAL CONTACT AND/OR INHALATION EXPOSURE, BASED ON THE WEIGHT OF SCIENTIFIC EVIDENCE SEE SECTION 16 FOR DEFINITIONS OF OTHER TERMS USED INTERNATIONAL OCCUPATIONAL EXPOSURE LIMITS: CURRENTLY, THE FOLLOWING ADDITIONAL EXPOSURE LIMIT VALUES HAVE BEEN ESTABLISHED BY VARIOUS COUNTRIES FOR THE COMPONENTS OF THIS MIXTURE. MORE CURRENT LIMITS MAY BE AVAILABLE; INDIVIDUAL COUNTRIES SHOULD BE CONSULTED TO DETERMINE IF NEWER LIMITS ARE AVAILABLE. ALUMINUM HYDROXIDE: AUSTRALIA: TWA: 2 MG(AL)/M3, JUL 2008 BELGIUM: TWA: 2 MG(Al)/M3, MAR 2002 FINLAND: TWA: 2 MG(Al)/M3, NOV 2011 FRANCE: VME: 2 MG(Al)/M3, FEB 2006 KOREA: TWA: 2 MG(Al)/M3, 2006 NEW ZEALAND: TWA: 2 MG(Al)/M3, JAN 2002 RUSSIA: TWA: 6 MG/M3, JUN 2003 SWEDEN: TWA: 1 MG(Al)/M3, JUN 2005 SWITZERLAND: MAK-W: 3 MG/M3, RESP, JAN 2011 UNITED KINGDOM: TWA: 2 MG(Al)/M3, OCT 2007 IN ARGENTINA, BULGARIA, COLOMBIA, JORDAN, SINGAPORE, VIETNAM CHECK ACGIH TLV CRYSTALLINE SILICA: AUSTRALIA: TWA: 0.1 MG/M3, JUL 2008 BELGIUM: TWA: 0.1 MG/M3 (RESP. DUST), MAR 2002 DENMARK: TWA: 0.1 MG/M3 (RESPIRABLE), CARC, MAY 2011 DENMARK: TWA: 0.1 MG/M3 (RESP.), CARC, MAY2011 DENMARK: TWA: 0.3 MG/M3 (TOTAL), MAY 2011 FINLAND: TWA: 0.05 MG/M3, RESP. DUST, SEP 2009 FRANCE: VME: 0.1 MG/M3, (RESP), FEB 2006 ICELAND: TWA: 0.1 MG/M3 (RESP. DUST), NOV 2011 JAPAN: OEL-C: 0.03 MG/M3 (RESPIRABLE), APR 2007 KOREA: TWA: 0.1 MG/M3, 2006 MEXICO: TWA: 0.1 MG/M3 (RESPIRABLE), 2004 THE NETHERLANDS: MAC-TGG: 0.075 MG/M3, 2003 NEW ZEALAND: TWA: 0.2 MG/M3 (RESPIRABLE DUST), JAN 2002 NORWAY: TWA: 0.1 MG/M3 (RESP. DUST), JAN 1999 NORWAY: TWA: 0.3 MG/M3 (TOTAL DUST), JAN 1999 PERU: TWA: 0.05 MG/M3, JUL 2005 RUSSIA: TWA: 1 MG/M3 STEL: 3 MG/M3, JUN 2003 SWEDEN: TWA: 0.1 MG/M3 (RESP. DUST), JUN 2005 SWITZERLAND: MAK-W: 0.15 MG/M3, DEC 2006 THAILAND: TWA: 10 MG/M3 (RESP. DUST), JAN 1993 THAILAND: TWA: 30 MG/M3 (TOTAL DUST), JAN 1993 UNITED KINGDOM: TWA: 0.1 MG/M3 (RESP. DUST), OCT 2007 IN ARGENTINA, BULGARIA, COLOMBIA, JORDAN, SINGAPORE, VIETNAM CHECK ACGIH TLV FORMALDEHYDE: ARAB REPUBLIC OF EGYPT: TWA: 2 PPM (3 MG/M3), JAN 1993 AUSTRALIA: TWA: 1 PPM (1.2 MG/M3) STEL: 2 PPM (2.5 MG/M3), CARCINOGEN, JUL 2008 AUSTRIA: MAK-TMW: 0.5 PPM (0.6 MG/M3) KZW: 0.5 PPM (0.6 MG/M3), SKIN, SEN, 2007 BELGIUM: STEL: 0.3 PPM (0.38 MG/M3), MAR 2002 DENMARK: CL: 0.3 PPM (0.4 MG/M3), CARC, MAY 2011 FINLAND: TWA: 0.3 PPM (0.37 MG/M3) CL: 1 PPM (1.2 MG/M3), NOV 2011 FRANCE: VME: 0.5 PPM, VLE 1 PPM, C3 CARCINOGEN, FEB 2006 GERMANY: MAK: 0.3 PPM (0.37 MG/M3), 2011 HUNGARY: TWA: 0.6 MG/M3 STEL: 0.6 MG/M3, SKIN, SEP 2000 ICELAND: TWA: 0.3 PPM (0.4 MG/M3) STEL: 1 PPM (1.2 MG/M3), SEN, NOV 2011 JAPAN: OEL: 0.1 PPM (0.12 MG/M3), 2A CARC, A2 SEN, S1 SEN, MAY 2012 JAPAN: OEL: 0.2 PPM (0.24 MG/M3), MAY 2012 KOREA: TWA: 1 PPM (1.5 MG/M3) STEL: 2 PPM (3 MG/M3), 2006 MEXICO: PEAK: 2 PPM (3 MG/M3), 2004 THE NETHERLANDS: MAC-TGG: 1.5 MG/M3, 2003 NEW ZEALAND: CL: 1 PPM (1.2 MG/M3), SEN, JAN 2002 NORWAY: TWA: 0.5 PPM (0.6 MG/M3), JAN 1999 PERU: TWA STEL: 0,3 PPM (0,37 MG/M3), JUL 2005 THE PHILIPPINES: TWA: 5 PPM (6 MG/M3), JAN 1993 POLAND: MAC(TWA): 0.5 MG/M3 MAC(STEL): 1 MG/M3, JAN 1999 RUSSIA: STEL: 0.5 MG/M3, SKIN, JUN 2003 SWEDEN: TWA: 0.5 PPM (0.6 MG/M3) CL: 1 PPM (1.2 MG/M3), CARCINOGEN, SEN, JUN 2005 SWITZERLAND: MAK-W: 0.3 PPM (0.37 MG/M3) KZG-W: 0.6 PPM (0.74 MG/M3), CARC 3, SEN, JAN 2011 THAILAND: TWA: 3 PPM STEL: 5 PPM, JAN 1993 TURKEY: TWA: 5 PPM (6 MG/M3), JAN 1993 UNITED KINGDOM: TWA: 2 PPM (2.5 MG/M3) STEL: 2 PPM (2.5 MG/M3), OCT 2007 IN ARGENTINA, BULGARIA, COLOMBIA, JORDAN, SINGAPORE, VIETNAM CHECK ACGIH TLV PHENOL: ARAB REPUBLIC OF EGYPT: TWA: 5 PPM (19 MG/M3), SKIN, JAN 1993 AUSTRALIA: TWA: 1 PPM (4 MG/M3), JUL 2008 AUSTRIA: MAK-TMW: 2 PPM (7.8 MG/M3), SKIN, 2007 DENMARK: TWA: 2 PPM (7.8 MG/M3), SKIN, MAR 2002 DENMARK: TWA: 1 PPM (4 MG/M3), SKIN, MAY 2011 EC: TWA: 7.8 MG/M3 (2 PPM), SKIN, JUN 2000 FINLAND: TWA: 2 PPM (8 MG/M3) STEL: 4 PPM (16 MG/M3), SKIN, NOV 2011 FRANCE: VME: 2 PPM (7.8 MG/M3), SKIN, FEB 2006 HUNGARY: TWA: 7.8 MG/M3 STEL: 78 MG/M3, SKIN, SEP 2000 ICELAND: TWA: 1 PPM (4 MG/M3), SKIN, NOV 2011 JAPAN: OEL: 5 PPM (19 MG/M3), SKIN, MAY 2012 KOREA: TWA: 5 PPM (19 MG/M3), SKIN, 2006 MEXICO: TWA: 5 PPM (19 MG/M3) STEL: 10 PPM (38 MG/M3) (SKIN), 2004 THE NETHERLANDS: MAC-TGG: 8 MG/M3, SKIN, 2003 NEW ZEALAND: TWA: 5 PPM (19 MG/M3), SKIN, JAN 2002 NORWAY: TWA: 1 PPM (4 MG/M3), JAN 1999 PERU: TWA: 5 PPM (19 MG/M3), JUL 2005 THE PHILIPPINES: TWA: 5 PPM (10 MG/M3), SKIN, JAN 1993 POLAND: MAC(TWA): 10 MG/M3 MAC(STEL): 20 MG/M3, JAN 1999 RUSSIA: TWA: 0.3 MG/M3 STEL: 1 MG/M3, SKIN, JUN 2003 SWEDEN: TWA: 1 PPM (4 MG/M3) STEL: 2 PPM (8 MG/M3), SKIN, JUN 2005 SWITZERLAND: CL: 5 PPM (19 MG/M3), SKIN, JAN 2011 THAILAND: TWA: 5 PPM (19 MG/M3), JAN 1993 TURKEY: TWA: 5 PPM (19 MG/M3), SKIN, JAN 1993 UNITED KINGDOM: TWA: 2 PPM (7.8 MG/M3), SKIN, OCT 2007 IN ARGENTINA, BULGARIA, COLOMBIA, JORDAN, SINGAPORE, VIETNAM CHECK ACGIH TLV PROTECTIVE EQUIPMENT: THE FOLLOWING INFORMATION ON APPROPRIATE PERSONAL PROTECTIVE EQUIPMENT IS PROVIDED TO ASSIST EMPLOYERS IN COMPLYING WITH OSHA REGULATIONS FOUND IN 29 CFR SUBPART I (BEGINNING AT 1910.132, INCLUDING U.S. FEDERAL OSHA RESPIRATORY PROTECTION (29 CFR 1910.134), OSHA EYE PROTECTION 29 CFR 1910.133, OSHA HARD PROTECTION 29 CFR 1910.138, OSHA FOOT PROTECTION 29 CFR 1910.136 AND OSHA BODY PROTECTION 29 CFR1910.132), EQUIVALENT STANDARDS OF CANADA (INCLUDING CSA RESPIRATORY STANDARD Z94.4-02, Z94.3-M1982, INDUSTRIAL EYE AND FACE PROTECTORS AND CSA STANDARD Z195-02, PROTECTIVE FOOTWEAR), OR STANDARDS OF JAPAN (INCLUDING JIS T 8116:2005 FOR GLOVE SELECTION, JIS T 8150:2006 FOR RESPIRATORY PPE, JIS T 8147:2003 FOR EYE PROTECTORS, AND JIS T 8030:2005 FOR PROTECTIVE CLOTHING). PLEASE REFERENCE APPLICABLE REGULATIONS AND STANDARDS FOR RELEVANT DETAILS. RESPIRATORY PROTECTION: MAINTAIN AIRBORNE CONTAMINANT CONCENTRATIONS BELOW EXPOSURE LIMITS LISTED ABOVE. FOR MATERIALS WITHOUT LISTED EXPOSURE LIMITS, MINIMIZE RESPIRATORY EXPOSURE. IF NECESSARY, USE ONLY RESPIRATORY PROTECTION AUTHORIZED UNDER APPROPRIATE REGULATIONS. EYE PROTECTION: WEAR SPLASH GOGGLES OR SAFETY GLASSES AS APPROPRIATE FOR THE TASK. HAND PROTECTION: DURING MANUFACTURE OR OTHER SIMILAR OPERATIONS, WEAR THE APPROPRIATE HAND PROTECTION FOR THE PROCESS. SKIN PROTECTION: USE APPROPRIATE PROTECTIVE CLOTHING. IF NECESSARY, REFER TO THE U.S. OSHA TECHNICAL MANUAL (SECTION VII: PERSONAL PROTECTIVE EQUIPMENT) OR OTHER APPROPRIATE REGULATIONS. FULL-BODY CHEMICAL PROTECTIVE CLOTHING IS RECOMMENDED FOR EMERGENCY RESPONSE PROCEDURES.
FORM: PUTTY COLOR: RED. MOLECULAR FORMULA: MIXTURE. MOLECULAR WEIGHT: MIXTURE. ODOR: MINIMAL. ODOR THRESHOLD: NOT AVAILABLE. FLAMMABLE LIMITS (IN AIR BY VOLUME, %): NOT APPLICABLE. OXIDIZING PROPERTIES: NOT APPLICABLE. DECOMPOSITION TEMPERATURE: NOT AVAILABLE. PERCENT VOLATILE: NOT AVAILABLE. AUTOIGNITION TEMPERATURE: NOT AVAILABLE. FLASH POINT: NOT AVAILABLE. FREEZING/MELTING POINT: NOT AVAILABLE. BOILING POINT: NOT AVAILABLE. VAPOR PRESSURE: NOT AVAILABLE. SPECIFIC GRAVITY (WATER = 1): 1.49 VAPOR DENSITY (AIR = 1): NOT AVAILABLE. CARB VOC: NOT AVAILABLE. EVAPORATION RATE (N-BUAC = 1): NOT APPLICABLE SCAQMD (U.S. EPA METHOD 24): NOT AVAILABLE. SOLUBILITY IN WATER: INSOLUBLE. SOLUBILITY IN SOLVENTS: NOT AVAILABLE. COEFFICIENT WATER/OIL DISTRIBUTION: NOT ESTABLISHED. PH: NOT AVAILABLE. HOW TO DETECT THIS SUBSTANCE (WARNING PROPERTIES IN EVENT OF ACCIDENTAL RELEASE): THE APPEARANCE MAY BE CHARACTERISTICS TO DISTINGUISH A RELEASE OF THIS PRODUCT.
CHEMICAL STABILITY: THIS PRODUCT IS STABLE WHEN PROPERLY STORED AT NORMAL TEMPERATURE AND PRESSURES (SEE SECTION 7, HANDLING AND STORAGE). DECOMPOSITION PRODUCTS: COMBUSTION: IF EXPOSED TO EXTREMELY HIGH TEMPERATURES, THERMAL DECOMPOSITION MAY GENERATE IRRITATING FUMES AND TOXIC GASES HYDROLYSIS: NONE KNOWN. MATERIALS WITH WHICH SUBSTANCE IS INCOMPATIBLE: THIS PRODUCT IS INCOMPATIBLE WITH STRONG OXIDIZERS. POSSIBILITY OF HAZARDOUS POLYMERIZATION OR REACTION: WILL NOT OCCUR. CONDITIONS TO AVOID: AVOID EXPOSURE TO OR CONTACT WITH EXTREME TEMPERATURES AND INCOMPATIBLE CHEMICALS.
HAZARDOUS MATERIAL IDENTIFICATION SYSTEM: HEALTH HAZARD (BLUE) 2* FLAMMABILITY HAZARD (RED) 0 PHYSICAL HAZARD(YELLOW) 0 PROTECTIVE EQUIPMENT: EYES: CHEMICAL GOGGLES RESPIRATORY: SEE SECTION 8 HANDS: GLOVES BODY: SEE SECTION 8 FOR ROUTINE INDUSTRIAL USE AND HANDLING APPLICATIONS HAZARD SCALE: 0=MINIMAL 1=SLIGHT 2=MODERATE 3=SERIOUS 4=SEVERE *=CHRONIC HAZARD SYMPTOMS OF EXPOSURE BY ROUTE OF EXPOSURE: THE HEALTH HAZARD INFORMATION PROVIDED BELOW IS PERTINENT TO EMPLOYEES USING THIS PRODUCT IN AN OCCUPATIONAL SETTING. THE FOLLOWING PARAGRAPHS DESCRIBE THE SYMPTOMS OF EXPOSURE BY ROUTE OF EXPOSURE. INHALATION: INHALATION OF FUMES OR VAPORS IF HEATED MAY CAUSE IRRITATION OF THE NOSE, THROAT, AND LUNGS AND CAUSE COUGHING. REMOVAL TO FRESH AIR SHOULD RELIEVE SYMPTOMS. THE TRACE CRYSTALLINE SILICA AND FORMALDEHYDE COMPONENTS ARE KNOWN HUMAN CARCINOGENS. DUE TO THE FORM OF THIS PRODUCT, THIS HAZARD IS NOT AS SIGNIFICANT DUE TO VISCOSITY AND CONSISTENCY OF THE MIXTURE. CONTACT WITH SKIN OR EYES: DIRECT EYE CONTACT MAY CAUSE IRRITATION, REDNESS, AND TEARING FROM MECHANICAL IRRITATION. PROLONGED OR REPEATED SKIN EXPOSURES MAY CAUSE DERMATITIS (DRY RED SKIN). SKIN ABSORPTION: THE PHENOL COMPONENT AND TRACE FORMALDEHYDE COMPONENT CAN BE ABSORBED THROUGH INTACT SKIN. PHENOL IN ALL FORMS (SOLID, SOLUTIONS AND VAPOR) IS READILY ABSORBED THROUGH THE SKIN AND CAN CAUSE HARMFUL EFFECTS IF A LARGE AREA OF THE SKIN IS INVOLVED OR IF CONTACT IS PROLONGED. DUE TO THE SMALL AMOUNT OF EACH OF THESE MATERIALS, THE POSSIBILITY OF ADVERSE EFFECTS IS NOT EXPECTED TO BE SIGNIFICANT HOWEVER, SKIN CONTACT SHOULD BE AVOIDED. FORMALDEHYDE AND PHENOL CAN CAUSE SENSITIZATION EFFECTS AS DESCRIBED UNDER 'SENSITIZATION EFFECT'S'. INGESTION: INGESTION IS NOT A SIGNIFICANT ROUTE OF OCCUPATIONAL EXPOSURE AND IS UNLIKELY TO OCCUR. IF THIS PRODUCT IS SWALLOWED, IRRITATION OF THE MOUTH, THROAT, ESOPHAGUS AND OTHER TISSUES OF THE DIGESTIVE SYSTEM MAY OCCUR. SYMPTOMS OF INGESTION MAY INCLUDE NAUSEA, VOMITING, AND DIARRHEA. INJECTION: ACCIDENTAL INJECTION OF THIS PRODUCT, VIA LACERATION OR PUNCTURE BY A CONTAMINATED OBJECT CAN CAUSE REDNESS AT THE SITE OF INJECTION. HEALTH EFFECTS OR RISKS FROM EXPOSURE: EXPOSURE TO THIS PRODUCT MAY CAUSE THE FOLLOWING HEALTH EFFECTS: ACUTE: INHALATION OF FUMES OR VAPORS MAY CAUSE IRRITATION OF RESPIRATORY SYSTEM. EYE CONTACT MAY CAUSE MECHANICAL IRRITATION. EYE CONTACT WITH FUMES CAN CAUSE IRRITATION. MAY BE HARMFUL IF SWALLOWED. CHRONIC: PROLONGED OR REPEATED SKIN EXPOSURE MAY CAUSE DERMATITIS (DRY RED SKIN). TARGET ORGANS: ACUTE: SKIN, EYES, RESPIRATORY SYSTEM. CHRONIC: SKIN. TOXICITY DATA: CURRENTLY, THE FOLLOWING TOXICOLOGICAL DATA ARE AVAILABLE FOR COMPONENTS OF 1% OR MORE CONCENTRATION. ALUMINUM TRIHYDRATE: TDLO (ORAL-CHILD): 79 GM/KG/2 YEARS-INTERMITTENT: BEHAVIORAL: CHANGES IN MOTOR ACTIVITY (SPECIFIC ASSAY), MUSCLE CONTRACTION OR SPASTICITY MUSCULOSKELETAL: OSTEOMALACIA TDLO (ORAL-CHILD): 122 GM/KG/4 DAYS: GASTROINTESTINAL: OTHER CHANGES NUTRITIONAL AND GROSS METABOLIC: BODY TEMPERATURE INCREASE TDLO (ORAL-WOMAN): 84 GM/KG: FEMALE 1-40 WEEK(S) AFTER CONCEPTION: REPRODUCTIVE: EFFECTS ON NEWBORN: PHYSICAL TDLO (ORAL-INFANT): 68040 MG/KG/24 WEEKS-INTERMITTENT: MUSCULOSKELETAL: OSTEOPOROSIS NUTRITIONAL AND GROSS METABOLIC: WEIGHT LOSS OR DECREASED WEIGHT GAIN, CHANGES IN PHOSPHORUS TDLO (ORAL-WOMAN): 73912.5 MG/KG/26 WEEKS-INTERMITTENT: BLOOD: CHANGES IN SERUM COMPOSITION (E.G. TP, BILIRUBIN, CHOLESTEROL) MUSCULOSKELETAL: OSTEOPOROSIS NUTRITIONAL AND GROSS: METABOLIC: CHANGES IN PHOSPHORUS TDLO (UNREPORTED-INFANT): 39 GM/KG/24 DAYS-INTERMITTENT: MUSCULOSKELETAL: OSTEOMALACIA TDLO (ORAL-RAT): 15 MG/KG: GASTROINTESTINAL: OTHER CHANGES TDLO (ORAL-RAT): 8040 MG/KG/67 DAYS-CONTINUOUS: BLOOD: CHANGES IN SERUM COMPOSITION (E.G. TP, BILIRUBIN, CHOLESTEROL) NUTRITIONAL AND GROSS METABOLIC: CHANGES IN PHOSPHORUS TDLO (ORAL-MOUSE): 80,880 MG/KG/23 WEEKS-CONTINUOUS: LIVER: OTHER CHANGES MUSCULOSKELETAL: OTHER CHANGES NUTRITIONAL AND GROSS METABOLIC: CHANGES IN METALS, NOT OTHERWISE SPECIFIED TDLO (INTRAPERITONEAL-RAT): 150 MG/KG TDLO (INTRAPERITONEAL-RAT): 6240 MG/KG/26 WEEKS-INTERMITTENT: BLOOD: PIGMENTED OR NUCLEATED RED BLOOD CELLS NUTRITIONAL AND GROSS METABOLIC: WEIGHT LOSS OR DECREASED WEIGHT GAIN, CHANGES IN IRON TDLO (INTRAPERITONEAL-RAT): 1920 MG/KG/8 WEEKS-INTERMITTENT: BLOOD: MICROCYTOSIS WITH OR WITHOUT ANEMIA TDLO (INTRAPERITONEAL-RAT): 960 MG/KG/4 WEEKS-INTERMITTENT: BLOOD: CHANGES IN ERYTHROCYTE (RBC) COUNT TDLO (ORAL-CHILD): 79 GM/KG/2 YEARS-INTERMITTENT: BEHAVIORAL: CHANGES IN MOTOR ACTIVITY (SPECIFIC ASSAY), MUSCLE CONTRACTION OR SPASTICITY MUSCULOSKELETAL: OSTEOMALACIA TDLO (ORAL-CHILD): 122 GM/KG/4 DAYS: GASTROINTESTINAL: OTHER CHANGES NUTRITIONAL AND GROSS METABOLIC: BODY TEMPERATURE INCREASE TDLO (ORAL-WOMAN): 84 GM/KG: FEMALE 1-40 WEEK(S) AFTER CONCEPTION: REPRODUCTIVE: EFFECTS ON NEWBORN: PHYSICAL TDLO (ORAL-INFANT): 68040 MG/KG/24 WEEKS-INTERMITTENT: MUSCULOSKELETAL: OSTEOPOROSIS NUTRITIONAL AND GROSS METABOLIC: WEIGHT LOSS OR DECREASED WEIGHT GAIN, CHANGES IN PHOSPHORUS TDLO (ORAL-WOMAN): 73912.5 MG/KG/26 WEEKS-INTERMITTENT: BLOOD: CHANGES IN SERUM COMPOSITION (E.G. TP, BILIRUBIN, CHOLESTEROL) MUSCULOSKELETAL: OSTEOPOROSIS NUTRITIONAL AND GROSS: METABOLIC: CHANGES IN PHOSPHORUS TDLO (UNREPORTED-INFANT): 39 GM/KG/24 DAYS-INTERMITTENT: MUSCULOSKELETAL: OSTEOMALACIA TDLO (ORAL-RAT): 15 MG/KG: GASTROINTESTINAL: OTHER CHANGES TDLO (ORAL-RAT): 8040 MG/KG/67 DAYS-CONTINUOUS: BLOOD: CHANGES IN SERUM COMPOSITION (E.G. TP, BILIRUBIN, CHOLESTEROL) NUTRITIONAL AND GROSS METABOLIC: CHANGES IN PHOSPHORUS TDLO (ORAL-MOUSE): 80,880 MG/KG/23 WEEKS-CONTINUOUS: LIVER: OTHER CHANGES MUSCULOSKELETAL: OTHER CHANGES NUTRITIONAL AND GROSS METABOLIC: CHANGES IN METALS, NOT OTHERWISE SPECIFIED TDLO (INTRAPERITONEAL-RAT): 150 MG/KG TDLO (INTRAPERITONEAL-RAT): 6240 MG/KG/26 WEEKS-INTERMITTENT: BLOOD: PIGMENTED OR NUCLEATED RED BLOOD CELLS NUTRITIONAL AND GROSS METABOLIC: WEIGHT LOSS OR DECREASED WEIGHT GAIN, CHANGES IN IRON TDLO (INTRAPERITONEAL-RAT): 1920 MG/KG/8 WEEKS-INTERMITTENT: BLOOD: MICROCYTOSIS WITH OR WITHOUT ANEMIA TDLO (INTRAPERITONEAL-RAT): 960 MG/KG/4 WEEKS-INTERMITTENT: BLOOD: CHANGES IN ERYTHROCYTE (RBC) COUNT PHENOL: LDLO (ORAL-HUMAN): 14 GM/KG: BEHAVIORAL: MUSCLE WEAKNESS LUNGS, THORAX, OR RESPIRATION: CYANOSIS LDLO (ORAL-HUMAN): 140 MG/KG: BEHAVIORAL: HALLUCINATIONS, DISTORTED PERCEPTIONS SKIN AND APPENDAGES: SWEATING LDLO (ORAL-INFANT): 10 MG/KG: BEHAVIORAL: MUSCLE WEAKNESS LUNGS, THORAX, OR RESPIRATION: CYANOSIS TDLO (PARENTERAL-MAN): 105.3 MG/KG: PERIPHERAL NERVE AND SENSATION: SENSORY CHANGE INVOLVING PERIPHERAL NERVE LUNGS, THORAX, OR RESPIRATION: DYSPNEA KIDNEY/URETER/BLADDER: RENAL FUNCTION TESTS DEPRESSED TDLO (UNREPORTED-MAN): 5714 (MICRO)G/KG: SENSE ORGANS AND SPECIAL SENSES (OLFACTION): EFFECT, NOT OTHERWISE SPECIFIED IC50 (IN VITRO-HUMAN LIVER): 3.02 MMOL/L/24 HOURS: IN VITRO TOXICITY STUDIES: CELL VIABILITY (MITOCHONDRIAL REDUCTASE ASSAYS): MTT, XTT, MTS, WSTS ASSAYS ETC IC50 (IN VITRO-HUMAN LIVER): 9.67 MMOL/L/24 HOURS: IN VITRO TOXICITY STUDIES: CELL VIABILITY (MITOCHONDRIAL REDUCTASE ASSAYS): MTT, XTT, MTS, WSTS ASSAYS ETC IC50 (IN VITRO-HUMAN LIVER TUMOR): 10 MMOL/L/24 HOURS: IN VITRO TOXICITY STUDIES: CELL PROTEIN SYNTHESIS IC50 (IN VITRO-HUMAN LIVER TUMOR): 3.47 MMOL/L/24 HOURS: IN VITRO TOXICITY STUDIES: CELL MEMBRANE INTEGRITY: CYTOPLASMIC ENZYMES LEAKAGE (LACTATE DEHYDROGENASE, ATP ENZYMES ETC.), CELL VIABILITY (MITOCHONDRIAL REDUCTASE ASSAYS): MTT, XTT, MTS, WSTS ASSAYS ETC IC50 (IN VITRO-HUMAN LIVER TUMOR): 14.66 MMOL/L/24 HOURS: IN VITRO TOXICITY STUDIES: CELL MEMBRANE INTEGRITY: CYTOPLASMIC ENZYMES LEAKAGE (LACTATE DEHYDROGENASE, ATP ENZYMES ETC.), CELL VIABILITY (MITOCHONDRIAL REDUCTASE ASSAYS): MTT, XTT, MTS, WSTS ASSAYS ETC IC50 (IN VITRO-HUMAN HELA CELL): 100 MG/L/24 HOURS: IN VITRO TOXICITY STUDIES: CELL MEMBRANE INTEGRITY: CYTOPLASMIC ENZYMES LEAKAGE (LACTATE DEHYDROGENASE, ATP ENZYMES ETC.) OPEN IRRITATION TEST (SKIN-RABBIT): 535 MG: SEVERE STANDARD DRAIZE TEST (SKIN-RABBIT): 100 MG: MILD STANDARD DRAIZE TEST (EYE-RABBIT): 5 MG: SEVERE STANDARD DRAIZE TEST (EYE-RABBIT): 400 (MICRO)L/30 SECONDS: SEVERE RINSED WITH WATER (EYE-RABBIT): 5 MG/30 SECONDS: MILD LC50 (INHALATION-RAT): 316 MG/M3 LC50 (INHALATION-RAT): 316 MG/M3/4 HOURS LC50 (INHALATION-MOUSE): 177 MG/M3 LC50 (INHALATION-MOUSE): 177 MG/M3/4 HOURS LD50 (ORAL-RAT): 317 MG/KG: BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD LD50 (ORAL-RAT): 512 MG/KG LD50 (ORAL-MOUSE): 270 MG/KG LD50 (ORAL-MAMMAL-SPECIES UNSPECIFIED): 500 MG/KG LD50 (SKIN-RAT): 1500 MG/KG LD50 (SKIN-RAT): 669 MG/KG: BEHAVIORAL: TREMOR KIDNEY/URETER/BLADDER: HEMATURIA SKIN AND APPENDAGES: CUTANEOUS SENSITIZATION, EXPERIMENTAL (AFTER TOPICAL EXPOSURE) LD50 (SKIN-RABBIT): 630 MG/KG LD50 (INTRAPERITONEAL-RAT): 127 MG/KG LD50 (INTRAPERITONEAL-MOUSE): 180 MG/KG LD50 (SUBCUTANEOUS-RAT): 300 MG/KG LD50 (SUBCUTANEOUS-MOUSE): 344 MG/KG LD50 (INTRAVENOUS-MOUSE): 112 MG/KG: BEHAVIORAL: TREMOR IC10 (IN VITRO-RAT LIVER): 1.12 MMOL/L/24 HOURS: IN VITRO TOXICITY STUDIES: CELL MEMBRANE INTEGRITY: CYTOPLASMIC ENZYMES LEAKAGE (LACTATE DEHYDROGENASE, ATP ENZYMES ETC.), CELL VIABILITY (MITOCHONDRIAL REDUCTASE ASSAYS): MTT, XTT, MTS, WSTS ASSAYS ETC IC10 (IN VITRO-RAT LUNG): 0.03 GM/L/24 HOURS: IN VITRO TOXICITY STUDIES: CELL MEMBRANE INTEGRITY (PRELABELED CELLS): RELEASE OF RADIOACTIVE ISOTOPES ([51CR], [3H]-THYMIDINE, [3H]-PROLINE, [35S]- OR [75SE]-METHIONINE, 5-[125I]-2-DEOXY-URIDINE) OR FLUORESCENT DYES (BIS-CARBOXYETHYL-CARBOXYFLUORESCEIN (BCECF) OR CALCEIN-AM) TIVIEQ IC10 (IN VITRO-RAT LUNG): 0.2 GM/L/24 HOURS: IN VITRO TOXICITY STUDIES: CELL VIABILITY (MITOCHONDRIAL REDUCTASE ASSAYS): MTT, XTT, MTS, WSTS ASSAYS ETC IC10 (IN VITRO-CHICKEN NEURONS): 7470 (MICRO)MOL/L/21 HOUR.....IN VITRO TOXICITY STUDIES: CELL VIABILITY (MITOCHONDRIAL REDUCTASE ASSAYS): MTT, XTT, MTS, WSTS ASSAYS ETC IC10 (IN VITRO-CHICKEN NEURONS): 1862 (MICRO)MOL/L/21 HOURS: IN VITRO TOXICITY STUDIES: CELL VIABILITY (MITOCHONDRIAL REDUCTASE ASSAYS): MTT, XTT, MTS, WSTS ASSAYS ETC IC10 (IN VITRO-CHICKEN NEURONS): 614 (MICRO)MOL/L/20 HOURS: IN VITRO TOXICITY STUDIES: CELL VIABILITY (LYSOSOMAL DAMAGE): NEUTRAL RED ASSAY ETC. IC50 (IN VITRO-RAT LIVER): 3.3 MMOL/L/24 HOURS: IN VITRO TOXICITY STUDIES: CELL MEMBRANE INTEGRITY: CYTOPLASMIC ENZYMES LEAKAGE (LACTATE DEHYDROGENASE, ATP ENZYMES ETC.), CELL VIABILITY (MITOCHONDRIAL REDUCTASE ASSAYS): MTT, XTT, MTS, WSTS ASSAYS ETC. IC50 (IN VITRO-RAT LUNG): 1 GM/L/24 HOURS: IN VITRO TOXICITY STUDIES: CELL VIABILITY (MITOCHONDRIAL REDUCTASE ASSAYS): MTT, XTT, MTS, WSTS ASSAYS ETC. IC50 (IN VITRO-RAT LUNG): 0.36 GM/L/24 HOURS: IN VITRO TOXICITY STUDIES: CELL MEMBRANE INTEGRITY (PRELABELED CELLS): RELEASE OF RADIOACTIVE ISOTOPES ([51CR], [3H]-THYMIDINE, [3H]-PROLINE, [35S]- OR [75SE]-METHIONINE, 5-[125I]-2-DEOXY-URIDINE) OR FLUORESCENT DYES (BIS-CARBOXYETHYL-CARBOXYFLUORESCEIN (BCECF) OR CALCEIN-AM) TDLO (ORAL-MOUSE): 2800 MG/KG/10 DAYS-INTERMITTENT: BEHAVIORAL: TREMOR, ATAXIA TDLO (SKIN-MOUSE): 329 MG/KG/30 MINUTES: SKIN AND APPENDAGES: PRIMARY IRRITATION (AFTER TOPICAL EXPOSURE) BIOCHEMICAL: METABOLISM (INTERMEDIARY): OTHER, EFFECT ON INFLAMMATION OR MEDIATION OF INFLAMMATION TDLO (SKIN-MOUSE): 88.9 (MICRO)L/KG: BIOCHEMICAL: METABOLISM (INTERMEDIARY): EFFECT ON INFLAMMATION OR MEDIATION OF INFLAMMATION TDLO (SKIN-MOUSE): 16 GM/KG/40 WEEKS-INTERMITTENT: TUMORIGENIC: CARCINOGENIC BY RTECS CRITERIA SKIN AND APPENDAGES: TUMORS TDLO (INTRAPERITONEAL-RAT): 650 MG/KG/17 DAYS-INTERMITTENT: BLOOD: OTHER CHANGES TDLO (INTRAPERITONEAL-RAT): 600 MG/KG: FEMALE 12-14 DAY(S) AFTER CONCEPTION: REPRODUCTIVE: EFFECTS ON EMBRYO OR FETUS: FETOTOXICITY (EXCEPT DEATH, E.G., STUNTED FETUS) TDLO (INTRAPERITONEAL-MOUSE): 300 MG/KG: NUTRITIONAL AND GROSS METABOLIC: BODY TEMPERATURE DECREASE TDLO (INTRAPERITONEAL-MOUSE): 300 MG/KG: IMMUNOLOGICAL INCLUDING ALLERGIC: HYPERSENSITIVITY DELAYED TCLO (INHALATION-RAT): 110 MG/M3/4 HOURS: BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) BLOOD: CHANGES IN SERUM COMPOSITION (E.G. TP, BILIRUBIN, CHOLESTEROL) BIOCHEMICAL: ENZYME INHIBITION, INDUCTION, OR CHANGE IN BLOOD OR TISSUE LEVELS: PROTEASES TCLO (INHALATION-RAT): 150 UG/M3/8 HOURS/26 WEEKS-INTERMITTENT: KIDNEY/URETER/BLADDER: CHANGES IN TUBULES (INCLUDING ACUTE RENAL FAILURE, ACUTE TUBULAR NECROSIS) BIOCHEMICAL: ENZYME INHIBITION, INDUCTION, OR CHANGE IN BLOOD OR TISSUE LEVELS: PHOSPHATASES TCLO (INHALATION-RAT): 5 MG/M3/4 HOURS/17 WEEKS-INTERMITTENT: LIVER: LIVER FUNCTION TESTS IMPAIRED ENDOCRINE: EFFECT ON MENSTRUAL CYCLE BLOOD: CHANGES IN LEUKOCYTE (WBC) COUNT TCLO (INHALATION-RAT): 100 (MICRO)G/M3/24 HOURS/61 DAYS-CONTINUOUS: BEHAVIORAL: MUSCLE CONTRACTION OR SPASTICITY BLOOD: OTHER CHANGES BIOCHEMICAL: ENZYME INHIBITION, INDUCTION, OR CHANGE IN BLOOD OR TISSUE LEVELS: TRUE CHOLINESTERASE TCLO (INHALATION-RAT): 0.5 MG/M3/4 HOURS/122 DAYS-INTERMITTENT: BLOOD: CHANGES IN SERUM COMPOSITION (E.G. TP, BILIRUBIN, CHOLESTEROL) BIOCHEMICAL: ENZYME INHIBITION, INDUCTION, OR CHANGE IN BLOOD OR TISSUE LEVELS: MULTIPLE ENZYME EFFECTS TCLO (INHALATION-MOUSE): 15 PPM/6 MINUTES: LUNGS, THORAX, OR RESPIRATION: RESPIRATORY DEPRESSION LCLO (INHALATION-RAT): 232 MG/M3/4 HOURS LCLO (INHALATION-MOUSE): 110 MG/M3/4 HOURS MUTATION TEST SYSTEMS-NOT OTHERWISE SPECIFIED (HUMAN HELA CELL): 17 MG/L MUTATION TEST SYSTEMS-NOT OTHERWISE SPECIFIED (HUMAN LYMPHOCYTE): 5 (MICRO)MOL/L DNA INHIBITION (HUMAN HELA CELL): 1 MMOL/L SISTER CHROMATID EXCHANGE (HUMAN LYMPHOCYTE): 5 (MICRO)MOL/L CYTOGENETIC ANALYSIS (HUMAN CELLS-NOT OTHERWISE SPECIFIED): 300 (MICRO)MOL/L/30 HOURS MUTATION IN MICROORGANISMS (BACTERIA-SA/MONE//A TYPHIMURIUM): 40 (MICRO)MOL/PLATE MUTATION IN MICROORGANISMS (MOUSE LYMPHOCYTE): 300 MG/L MUTATION IN MICROORGANISMS (MICROORGANISM-NOT OTHERWISE SPECIFIED): 200 MG/L/8 HOURS SEX CHROMOSOME LOSS AND NON-DISJUNCTION (INSECT-DROSOPHILA ME/ANOGASTER OVARY): 100 PPM GENE CONVERSION AND MITOTIC RECOMBINATION (MOLD-ASPERGI//US NIDU/ANS): 15 (MICRO)MOL/L DNA DAMAGE (MAMMAL-SPECIES UNSPECIFIED LYMPHOCYTE): 250 MMOL/L MICRONUCLEUS TEST (ORAL-MOUSE): 265 MG/KG MICRONUCLEUS TEST (INTRAPERITONEAL-MOUSE): 265 MG/KG MICRONUCLEUS TEST (HAMSTER LUNG): 4 MMOL/L MICRONUCLEUS TEST (HAMSTER OVARY): 175 MG/L MICRONUCLEUS TEST (HAMSTER EMBRYO): 500 MG/L/4 HOURS DNA INHIBITION (ORAL-MOUSE): 20 GM/KG DNA INHIBITION (MOUSE LYMPHOCYTE): 800 (MICRO)MOL/L DNA INHIBITION (HAMSTER LUNG): 1900 (MICRO)MOL/L CYTOGENETIC ANALYSIS (MULTIPLE ROUTES-FISH-NOT OTHERWISE SPECIFIED): 300 NL/L CYTOGENETIC ANALYSIS (HAMSTER OVARY): 2 GM/L CYTOGENETIC ANALYSIS (HAMSTER EMBRYO): 100 (MICRO)MOL/L UNSCHEDULED DNA SYNTHESIS (ORAL-RAT): 4 GM/KG UNSCHEDULED DNA SYNTHESIS (HAMSTER EMBRYO): 3 (MICRO)MOL/L DNA DAMAGE (MOUSE LYMPHOCYTE): 1500 (MICRO)MOL/L MUTATION TEST SYSTEMS-NOT OTHERWISE SPECIFIED (MOUSE CELLS-NOT OTHERWISE SPECIFIED): 2500 (MICRO)MOL/L MUTATION TEST SYSTEMS-NOT OTHERWISE SPECIFIED (RABBIT BONE MARROW): 250 (MICRO)MOL/L MUTATION IN MAMMALIAN SOMATIC CELLS (MOUSE LYMPHOCYTE MOUSE LYMPHOCYTE): 1890 (MICRO)MOL/L MUTATION IN MAMMALIAN SOMATIC CELLS (HAMSTER EMBRYO): 3 MMOL/L MORPHOLOGICAL TRANSFORMATION (HAMSTER EMBRYO): 10 (MICRO)MOL/L SISTER CHROMATID EXCHANGE (HAMSTER OVARY): 300 MG/L SISTER CHROMATID EXCHANGE (HAMSTER EMBRYO): 1 MMOL/L POLYBUTENE: TCLO (INHALATION-RAT): 700 MG/M3/7 HOURS/2 WEEKS-INTERMITTENT: LIVER: CHANGES IN LIVER WEIGHT NUTRITIONAL AND GROSS METABOLIC: WEIGHT LOSS OR DECREASED WEIGHT GAIN IRRITANCY OF PRODUCT: INHALATION OF FUMES OR VAPORS MAY CAUSE RESPIRATORY IRRITATION. EYE CONTACT MAY CAUSE IRRITATION. EYE CONTACT WITH FUMES MAY CAUSE IRRITATION. PROLONGED SKIN CONTACT MAY CAUSE IRRITATION. CARCINOGENIC POTENTIAL OF COMPONENTS: COMPONENTS OF THIS PRODUCT ARE LISTED BY AGENCIES TRACKING THE CARCINOGENIC POTENTIAL OF CHEMICAL COMPOUNDS, AS FOLLOWS: CRYSTALLINE SILICA: ACGIH-TLV-A2 (SUSPECTED HUMAN CARCINOGEN); IARC-1 (CARCINOGENIC TO HUMANS); MAK-1 (SUBSTANCES THAT CAUSE CANCER IN MAN AND CAN BE ASSUMED TO MAKE A SIGNIFICANT CONTRIBUTION TO CANCER RISK); NIOSH-CA (POTENTIAL OCCUPATIONAL CARCINOGEN WITH NO FURTHER CATEGORIZATION); NTP-K (KNOWN TO BE A HUMAN CARCINOGEN) FORMALDEHYDE: ACGIH-TLV-A2 (SUSPECTED HUMAN CARCINOGEN); EPA-B1 (PROBABLE HUMAN CARCINOGEN-LIMITED EVIDENCE OF CARCINOGENICITY FROM EPIDEMIOLOGICAL STUDIES), IARC-1 (CARCINOGENIC TO HUMANS); MAK-4 (SUBSTANCES WITH CARCINOGENIC POTENTIAL FOR WHICH GENOTOXICITY PLAYS NO OR AT MOST A MINOR ROLE. NO SIGNIFICANT CONTRIBUTION TO HUMAN CANCER RISK IS EXPECTED, PROVIDED THE MAK VALUE IS OBSERVED.); NIOSH-CA (POTENTIAL OCCUPATIONAL CARCINOGEN WITH NO FURTHER CATEGORIZATION); NTP-K (KNOWN TO BE A HUMAN CARCINOGEN); OSHA-CA (CARCINOGEN DEFINED WITH NO FURTHER CATEGORIZATION) PHENOL: ACGIH TLV-A4 (NOT CLASSIFIABLE AS A HUMAN CARCINOGEN); EPA-I (DATA ARE INADEQUATE FOR AN ASSESSMENT OF HUMAN CARCINOGENIC POTENTIAL); EPA-D (NOT CLASSIFIABLE AS TO HUMAN CARCINOGENICITY); IARC-3 (UNCLASSIFIABLE AS TO CARCINOGENICITY IN HUMANS); MAK-3B (SUBSTANCES FOR WHICH IN VITRO TESTS OR ANIMAL STUDIES HAVE YIELDED EVIDENCE OF CARCINOGENIC EFFECTS THAT IS NOT SUFFICIENT FOR CLASSIFICATION OF THE SUBSTANCE IN ONE OF THE OTHER CATEGORIES. FURTHER STUDIES ARE REQUIRED BEFORE A FINAL CLASSIFICATION CAN BE MADE.) THE REMAINING COMPONENTS ARE NOT FOUND ON THE FOLLOWING LISTS: U.S. EPA, U.S. NTP, U.S. OSHA, U.S. NIOSH, GERMAN MAK, IARC, OR ACGIH AND THEREFORE IS NEITHER CONSIDERED TO BE NOR SUSPECTED TO BE A CANCER-CAUSING AGENT BY THESE AGENCIES. REPRODUCTIVE TOXICITY INFORMATION: THIS PRODUCT IS NOT EXPECTED OR REPORTED TO CAUSE HUMAN MUTAGENIC, EMBRYOTOXIC, TERATOGENIC OR REPRODUCTIVE TOXICITY EFFECTS. THE FOLLOWING GIVES INFORMATION ON POSSIBLE EFFECTS FROM COMPONENTS. MUTAGENICITY: FORMALDEHYDE IS CONSIDERED MUTAGENIC, BASED ON POSITIVE RESULTS (E.G. CHROMOSOMAL ABERRATIONS IN LUNG CELLS) OBSERVED IN STUDIES WITH LIVE ANIMALS. IN OCCUPATIONAL EXPOSURE STUDIES, WHICH ARE LIMITED BY SUCH PROBLEMS AS LOW NUMBERS OF WORKERS STUDIED AND MIXED EXPOSURES, BOTH POSITIVE AND NEGATIVE RESULTS (MICRONUCLEI, SISTER CHROMATID EXCHANGES (SCES), CHROMOSOME ABERRATIONS IN LYMPHOCYTES OR CHEEK AND NOSE CELLS) AND A NEGATIVE RESULT (ABNORMAL SPERM) WERE OBTAINED.(19,44,46,81) HOWEVER, POSITIVE RESULTS (SCES IN LYMPHOCYTES, DNA-PROTEIN CROSSLINKS IN LYMPHOCYTES) WERE OBTAINED IN 2 REASONABLY WELL-CONDUCTED STUDIES. EMBRYOTOXICITY/TERATOGENICITY: NO COMPONENT IS KNOWN TO CAUSE HUMAN EMBRYOTOXICITY OR TERATOGENICITY. ANIMAL STUDIES ARE INCONCLUSIVE OR HAVE NOT SHOWN EMBRYOTOXICITY OR TERATOGENICITY. REPRODUCTIVE TOXICITY: THERE IS INSUFFICIENT EVIDENCE TO DETERMINE IF FORMALDEHYDE CAUSES REPRODUCTIVE TOXICITY IN HUMANS. DESPITE LIMITATIONS, THE FEW ANIMAL STUDIES AVAILABLE DO NOT SUGGEST THAT FORMALDEHYDE EXPOSURE WILL AFFECT FERTILITY. ACGIH BIOLOGICAL EXPOSURE INDICES (BEIS): CURRENTLY, THERE ARE NO ACGIH BIOLOGICAL EXPOSURE INDICES (BEIS) DETERMINED FOR THIS MATERIAL. DEGREE OF EFFECT TO THE HEALTH OF THE POLLUTING AGENT OF ENVIRONMENT OF WORK (PER MEXICAN NOM-010 STPS-1999): 0
ALL WORK PRACTICES MUST BE AIMED AT ELIMINATING ENVIRONMENTAL CONTAMINATION. MOBILITY: THIS PRODUCT HAS NOT BEEN TESTED FOR MOBILITY IN SOIL. PERSISTENCE AND BIODEGRADABILITY: THIS PRODUCT HAS NOT BEEN TESTED FOR PERSISTENCE OR BIODEGRADABILITY. THE MINERAL COMPONENTS ARE NOT EXPECTED TO BIODEGRADE TO GREAT EXTENT. BIO-ACCUMULATION POTENTIAL: THIS PRODUCT HAS NOT BEEN TESTED FOR BIO-ACCUMULATION POTENTIAL. ECOTOXICITY: THIS PRODUCT HAS NOT BEEN TESTED FOR AQUATIC OR ANIMAL TOXICITY. ALL RELEASES TO TERRESTRIAL, ATMOSPHERIC AND AQUATIC ENVIRONMENTS SHOULD BE AVOIDED. OTHER ADVERSE EFFECTS: THIS MATERIAL IS NOT LISTED AS HAVING OZONE DEPLETION POTENTIAL. ENVIRONMENTAL EXPOSURE CONTROLS: CONTROLS SHOULD BE ENGINEERED TO PREVENT RELEASE TO THE ENVIRONMENT, INCLUDING PROCEDURES TO PREVENT SPILLS, ATMOSPHERIC RELEASE AND RELEASE TO WATERWAYS.
DISPOSAL METHODS: IT IS THE RESPONSIBILITY OF THE GENERATOR TO DETERMINE AT THE TIME OF DISPOSAL WHETHER THE PRODUCT MEETS THE CRITERIA OF A HAZARDOUS WASTE PER REGULATIONS OF THE AREA IN WHICH THE WASTE IS GENERATED AND/OR DISPOSED OF. WASTE DISPOSAL MUST BE IN ACCORDANCE WITH APPROPRIATE FEDERAL, STATE, NATIONAL, INTERNATIONAL, AND LOCAL REGULATIONS. THIS PRODUCT, IF UNALTERED BY USE, MAY BE DISPOSED OF BY TREATMENT AT A PERMITTED FACILITY OR AS ADVISED BY YOUR LOCAL HAZARDOUS WASTE REGULATORY AUTHORITY. SHIPMENT OF WASTES MUST BE DONE WITH APPROPRIATELY PERMITTED AND REGISTERED TRANSPORTERS. DISPOSAL CONTAINERS: WASTE MATERIALS MUST BE PLACED IN AND SHIPPED IN APPROPRIATE 5-GALLON OR 55-GALLON POLY OR METAL WASTE PAILS OR DRUMS. ENSURE THAT ANY REQUIRED MARKING OR LABELING OF THE CONTAINERS BE DONE TO ALL APPLICABLE REGULATIONS. PRECAUTIONS TO BE FOLLOWED DURING WASTE HANDLING: WEAR PROPER PROTECTIVE EQUIPMENT WHEN HANDLING WASTE MATERIALS. U.S. EPA WASTE NUMBER: NOT APPLICABLE.
U.S. DEPARTMENT OF TRANSPORTATION REGULATIONS: THIS PRODUCT IS NOT CLASSIFIED AS DANGEROUS GOODS, PER U.S. DOT REGULATIONS, UNDER 49 CFR 172.101. TRANSPORT CANADA TRANSPORTATION OF DANGEROUS GOODS REGULATIONS: THIS PRODUCT IS NOT CLASSIFIED AS DANGEROUS GOODS, PER REGULATIONS OF TRANSPORT CANADA. INTERNATIONAL AIR TRANSPORT ASSOCIATION (IATA): THIS PRODUCT IS NOT CLASSIFIED AS DANGEROUS GOODS UNDER RULES OF IATA. INTERNATIONAL MARITIME ORGANIZATION (IMO) DESIGNATION: THIS PRODUCT IS NOT CLASSIFIED AS DANGEROUS GOODS BY THE INTERNATIONAL MARITIME ORGANIZATION. OFFICIAL MEXICAN STANDARD; REGULATION FOR THE TRANSPORT OF DANGEROUS GOODS AND RESIDUES: THIS PRODUCT IS NOT CLASSIFIED AS DANGEROUS GOODS, PER TRANSPORT REGULATIONS OF MEXICO. SINGAPORE STANDARD 286: PART A: THIS PRODUCT HAS NO REQUIREMENTS UNDER THE SPECIFICATION FOR CAUTION LABELING FOR HAZARDOUS SUBSTANCES PART 4: MARKING OF PACKAGES, CONTAINERS AND VEHICLES, AS IT DOES NOT MEET THE CRITERIA FOR ANY HAZARD CLASS UNDER THIS REGULATION. TRANSPORT IN BULK ACCORDING TO THE IBC CODE: SEE THE INFORMATION UNDER THE INDIVIDUAL JURISDICTION LISTINGS FOR IBC INFORMATION. ENVIRONMENTAL HAZARDS: THIS MATERIAL DOES NOT MEET THE CRITERIA OF ENVIRONMENTALLY HAZARDOUS ACCORDING TO THE CRITERIA OF THE UN MODEL REGULATIONS (AS REFLECTED IN THE IMDG CODE, ADR, RID, AND ADN) AND IS NOT LISTED IN ANNEX III UNDER MARPOL 73/78.
UNITED STATES REGULATIONS: U.S. SARA REPORTING REQUIREMENTS: THE COMPONENTS OF THIS PRODUCT ARE SUBJECT TO THE REPORTING REQUIREMENTS OF SECTIONS 302, 304, AND 313 OF TITLE III OF THE SUPERFUND AMENDMENTS AND REAUTHORIZATION ACT AS FOLLOWS. CHEMICAL NAME SARA 302 SARA 304 SARA 313 (40 CFR 355, (40 CFR TABLE (40 CFR 372.65) APPENDIX A) 302.4) FORMALDEHYDE YES YES YES PHENOL YES YES YES U.S. SARA HAZARD CATEGORIES (SECTION 311/312, 40 CFR 370-21): ACUTE: YES CHRONIC: YES FIRE: NO REACTIVE: NO SUDDEN RELEASE: NO U.S. SARA THRESHOLD PLANNING QUANTITY (TPQ): FORMALDEHYDE: 500 LB (27.2 KG) PHENOL: 500 LB (27.2 KG) U.S. CERCLA REPORTABLE QUANTITY (RQ): FORMALDEHYDE: 100 LB (45.4 KG) PHENOL: 1000 LB (454 KG) U.S. TSCA INVENTORY STATUS: COMPONENTS OF THIS PRODUCT ARE LISTED ON THE TSCA INVENTORY. CALIFORNIA SAFE DRINKING WATER AND TOXIC ENFORCEMENT ACT (PROPOSITION 65): THE CRYSTALLINE SILICA AND FORMALDEHYDE (GAS) COMPONENTS ARE ON THE CALIFORNIA PROPOSITION 65 LISTS. WARNING! THIS PRODUCT CONTAINS COMPOUNDS KNOWN TO THE STATE OF CALIFORNIA TO CAUSE CANCER. THIS PRODUCT CONTAINS TRACE AMOUNTS OF A SUSPECTED HUMAN CARCINOGEN BY INHALATION; HOWEVER, THIS HAZARD IS NOT EXPECTED TO BE SIGNIFICANT DUE TO VISCOSITY AND CONSISTENCY OF THE MIXTURE. CANADIAN REGULATIONS: CANADIAN DSL/NDSL INVENTORY STATUS: COMPONENTS ARE ON THE DSL OR NDSL INVENTORIES. CANADIAN ENVIRONMENTAL PROTECTION ACT (CEPA) PRIORITIES SUBSTANCES LISTS: THE PHENOL AND FORMALDEHYDE COMPONENTS ARE ON THE CEPA PRIORITIES SUBSTANCES 2 LIST. CANADIAN WHMIS CLASSIFICATION AND SYMBOLS: THIS PRODUCT WOULD BE CATEGORIZED AS A CONTROLLED PRODUCT, D2B (OTHER TOXIC EFFECTS-POTENTIAL CARCINOGENIC AND MUTAGENIC EFFECT, IRRITATION, SKIN SENSITIZATION) AS PER THE CONTROLLED PRODUCT REGULATIONS. D2 - MATERIALS CAUSING OTHER TOXIC EFFECTS CHINESE REGULATIONS: CHINESE INVENTORY OF EXISTING CHEMICAL SUBSTANCES STATUS: COMPONENTS LISTED BY CAS# ARE LISTED ON THE CHINESE INVENTORY OF EXISTING CHEMICAL SUBSTANCES (IECSC), OR ARE NOT LISTED, PER INFORMATION IN SECTION 2. JAPANESE REGULATIONS: JAPANESE ENCS: COMPONENTS LISTED BY CAS# ARE ON THE ENCS INVENTORY, ARE EXCEPTED, OR ARE NOT LISTED, PER INFORMATION IN SECTION 2. JAPANESE MINISTRY OF ECONOMY, TRADE, AND INDUSTRY (METI) STATUS: COMPONENTS ARE NOT LISTED AS CLASS I SPECIFIED CHEMICAL SUBSTANCES, CLASS II SPECIFIED CHEMICAL SUBSTANCES, OR DESIGNATED CHEMICAL SUBSTANCES BY THE JAPANESE METI. POISONOUS AND DELETERIOUS SUBSTANCES CONTROL LAW: COMPONENTS ARE NOT LISTED AS A SPECIFIED POISONOUS SUBSTANCE UNDER THE POISONOUS AND DELETERIOUS SUBSTANCES CONTROL LAW. KOREAN REGULATIONS: KOREAN EXISTING CHEMICALS LIST (ECL) STATUS: COMPONENTS LISTED BY CAS# ARE LISTED ON THE KOREAN ECL INVENTORY, OR ARE NOT LISTED, PER INFORMATION IN SECTION 2. MEXICAN REGULATIONS: MEXICAN WORKPLACE REGULATIONS (NOM-018-STPS-2000): THIS PRODUCT IS CLASSIFIED AS HAZARDOUS. SINGAPORE REGULATIONS: LIST OF CONTROLLED HAZARDOUS SUBSTANCES: COMPONENTS LISTED BY CAS# ARE NOT LISTED ON THE SINGAPORE LIST OF CONTROLLED SUBSTANCES. CODE OF PRACTICE ON POLLUTION CONTROL REQUIREMENTS: THE COMPONENTS IDENTIFIED BY CAS# IN SECTION 2 (COMPOSITION AND INFORMATION ON INGREDIENTS) NOT ARE SUBJECT TO THE REQUIREMENTS UNDER THE SINGAPORE CODE OF PRACTICE ON POLLUTION CONTROL. TAIWANESE REGULATIONS: TAIWAN EXISTING CHEMICAL SUBSTANCES INVENTORY STATUS: COMPONENTS LISTED BY CAS# ARE LISTED ON THE TAIWAN EXISTING CHEMICALS LIST.
REVISION DETAILS: NEW. REFERENCES AND DATA SOURCES: CONTACT THE SUPPLIER FOR INFORMATION. METHODS OF EVALUATING INFORMATION FOR THE PURPOSE OF CLASSIFICATION: CRITERIA OF THE GHS WERE USED FOR CLASSIFICATION. PREPARED BY: CHEMICAL SAFETY ASSOCIATES, INC. PO BOX 1961 HILO, HI 96721-1961 (800) 441 -3365 DATE OF PRINTING: JUNE 13, 2016 REVISION HISTORY: NEW. STI MARINE FIRESTOP PUTTY (MPU) SDS EFFECTIVE DATE: JUNE 13, 2016 SPECSEAL(R*) FIRESTOP PUTTY SDS EFFECTIVE DATE: JANUARY 4, 2015 |