AROCHLOR 1232

AROCHLOR 1232 Basic information
Product Name:AROCHLOR 1232
Synonyms:[40cfr136(1986)]pcb-1232;chlorodiphenyl(32%cl);polychlorinatedbiphenyl(aroclor1232);AROCLOR 1232, 1X1ML, ISO, 1UG/ML;AROCLOR 1232, 1X5ML, TRANSFORMER OIL 500 MG/KG;AROCLOR 1232, 10MG, NEAT;AROCLOR 1232, 1X1ML, MEOH, 1000UG/ML;AROCLOR 1232, 1X1ML, MEOH, 200UG/ML
CAS:11141-16-5
MF:N/A
MW:0
EINECS:
Product Categories:Method 8082International Standards;MISA Group 27 - Polychlorinated BiphenylsMore...Close...;Single Component SolutionsMore...Close...;8000 Series Solidwaste Methods;A;Alphabetic;AR to AZEnvironmental Standards;Aroclors, PCBs, and Dioxins;AroclorsEnvironmental Standards;AroclorsEPA;CLP Standards;Method 8082EPA;OLM04 Statement of WorkEnvironmental Standards;Separate Source Standards;Volatiles/ Semivolatiles;Environmental Standards;Aroclors;500 Series Drinking Water Methods;Canada;Method 505EPA;Method 508EPA
Mol File:Mol File
AROCHLOR 1232 Structure
AROCHLOR 1232 Chemical Properties
Melting point 47.61°C (estimate)
Boiling point 286.91°C (rough estimate)
density 1.2400 (estimate)
vapor pressure 4.6 x 10-3 mmHg at 25 °C (estimated, U.S. EPA, 1980a)
refractive index 1.5920 (estimate)
Fp 146 °C
storage temp. -20°C
form neat
Water Solubility 1.45 mg/L at 25 °C (Pal et al., 1980)
Henry's Law Constant8.64 (calculated, U.S. EPA, 1980a)
Exposure limitsNIOSH REL: TWA 1.0 μg/m3, IDLH 5 mg/m3.
EPA Substance Registry SystemAroclor 1232 (11141-16-5)
Safety Information
Hazard Codes N,Xi,Xn,F,T
Risk Statements 33-50/53-36/37/38-67-65-38-11-62-48/20-39/23/24/25-23/24/25-52/53-45-51/53
Safety Statements 35-60-61-36/37-26-62-33-29-16-9-45-53
RIDADR 2315
WGK Germany 3
RTECS TQ1354000
HazardClass 9
PackingGroup II
Hazardous Substances Data11141-16-5(Hazardous Substances Data)
ToxicityAcute oral LD50 for rats 4,470 mg/kg (quoted, RTECS, 1985).
MSDS Information
AROCHLOR 1232 Usage And Synthesis
Chemical PropertiesViscous, oily, colorless to light yellow, nonflammable, liquid with a faint, aromatic-type odor
UsesIn polyvinyl acetate to improve fiber-tear properties; as an insulator fluid for electric condensers and as an additive in very high pressure lubricants. In fluorescent and high-intensity discharge ballasts manufactured prior to 1979 (U.S. EPA, 1998).
May have been added to automotive transmission oils to swell shrunken transmission seals in place (Monsanto, 1960).
At a concentration of 5 to 25 wt %, increased the effective kill-life of the lindane spray up to 10 times. May have been used in chlordane and BHC insecticide formulations. In polyvinyl acetate emsulsions to impart strong bonding power in adhesives (Monsanto, 1960).

General DescriptionViscous oily liquid.
Air & Water ReactionsInsoluble in water.
Reactivity ProfileSimple aromatic halogenated organic compounds are very unreactive. Reactivity generally decreases with increased degree of substitution of halogen for hydrogen atoms.
Health HazardACUTE/CHRONIC HAZARDS: Toxic irritant. Hazardous decomposition products.
Fire HazardSome may burn but none ignite readily. Containers may explode when heated. Some may be transported hot.
Safety ProfileSuspected human carcinogen. Moderately toxic by skin contact. Mildly toxic by ingestion. When heated to decomposition it emits toxic fumes of Cl-. Used in heat transfer, hydraulic fluids, lubricants, and insecticides. See also POLYCHLORINATED BIPHENYLS.
Environmental fateBiological. Reported degradation products by the microorganism Alcaligenes BM-2 for a mixture of polychlorinated biphenyls include monohydroxychlorobiphenyl, 2-hydroxy-6-oxochlorophenylhexa- 2,4-dieonic acid, chlorobenzoic acid, chlorobenzoylpropionic acid, chlorophenylacetic acid, and 3-chlorophenyl-2-chloropropenic acid (Yagi and Sudo, 1980).
When PCB-1232 was statically incubated in the dark at 25 °C with yeast extract and settled domestic wastewater inoculum for 7 d, significant biodegradation with rapid adaptation was observed (Tabak et al., 1981).
Photolytic. PCB-1232 in a 90% acetonitrile/water solution containing 0.2 to 0.3 M sodium borohydride and irradiated with UV light (λ = 254 nm) reacted to yield dechlorinated biphenyls. Without sodium borohydride, the reaction proceeded more slowly (Epling et al., 1988).
Chemical/Physical. Zhang and Rusling (1993) evaluated the bicontinuous microemulsion of surfactant/oil/water as a medium for the dechlorination of polychlorinated biphenyls by electrochemical catalytic reduction. The microemulsion (20 mL) contained didodecyldimethylammonium bromide, dodecane, and water at concentrations of 21, 57, and 22 wt %, respectively. The catalyst used was zinc phthalocyanine (3.5 nM). When PCB-1232 (69 mg), the microemulsion and catalyst were subjected to an electrical current of mA/cm2 on 11.2 cm2 lead electrode for 12 h, a dechlorination yield of >99.8% was achieved. Reaction products included minor amounts of mono- and dichlorobiphenyls (0.01 mg), biphenyl, and reduced alkylbenzene derivatives.
PCB-1232 will not hydrolyze to any reasonable extent (Kollig, 1993).
At influent concentrations of 1.0, 0.1, 0.01, and 0.001 mg/L, the GAC adsorption capacities were 630, 120, 22, and 4.0 mg/g, respectively (Dobbs and Cohen, 1980).




AROCHLOR 1232 Preparation Products And Raw materials
AROCHLOR 5460 SOLUTION 100UG/ML IN METHANOL 1ML AROCHLOR 1232 SOLUTION 100UG/ML IN TRANSFORMER OIL 1ML AROCHLOR 6062 SOLUTION 100UG/ML IN METHANOL 1ML AROCHLOR 1232 SOLUTION 1000UG/ML IN HEXANE 1ML AROCHLOR 5432 SOLUTION 100UG/ML IN METHANOL 1ML AROCHLOR 5460 SOLUTION 100UG/ML IN METHANOL 5X1ML AROCHLOR 6062 1G [R] AROCHLOR 1232 SOLUTION 100UG/ML IN METHANOL 5X1ML AROCHLOR 6062 SOLUTION 100UG/ML IN METHANOL 5X1ML AROCHLOR 1232 SOLUTION 1000UG/ML IN HEXANE 5X1ML AROCHLOR 5432 SOLUTION 100UG/ML IN METHANOL 5X1ML AROCHLOR 5460 SOLUTION 100UG/ML IN METHANOL 5ML AROCHLOR 1232 SOLUTION 100UG/ML IN TRANSFORMER OIL 5ML AROCHLOR 1232 SOLUTION 100UG/ML IN METHANOL 5ML AROCHLOR 5432 1G [R] AROCHLOR 6062 SOLUTION 100UG/ML IN METHANOL 5ML AROCHLOR 1232 SOLUTION 1000UG/ML IN HEXANE 5ML AROCHLOR 5432 SOLUTION 100UG/ML IN METHANOL 5ML

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