11096-82-5

Basic information

• Product Name: AROCLOR 1260, 1X1ML, ISO, 1000UG/ML
• Synonyms: AROCLOR 1260, 1X1ML, ISO, 1000UG/ML;[40cfr136(1986)]pcb-1260;aroclor1260(pcb);aroclor1260referencestandardforclp;articlescontainingpolychlorinatedbiphenyls(pcb);IRIDIUM STAND;Aroclor 1260 (PCB 1260);chlorodiphenyl(60%cl)
• CAS NO: 11096-82-5
• Molecular Formula: C12H4Cl6
• Molecular Weight: 360.87816
• EINECS: 201-274-6
• Product Categories: Separate Source Standards;Single Component Solutions;2000/60/EC;A;Alphabetic;AR to AZEnvironmental Standards;Aroclors, PCBs, and Dioxins;AroclorsEnvironmental Standards;AroclorsMethod Specific;European Community: ISO and DIN;Volatiles/ Semivolatiles;8000 Series Solidwaste Methods;AroclorsEPA;CLP Standards;Method 8082EPA;OLM04 Statement of WorkEnvironmental Standards
• Mol File: 11096-82-5.mol
• Article Data: 0

Chemical Properties

• Melting Point: 115.76°C (estimate)
• Boiling Point: 457.69°C (rough estimate)
• Flash Point: 11 °C
• Appearance: /
• Density: 1.5800 (estimate)
• Vapor Pressure: 5.22E-06mmHg at 25°C
• Refractive Index: 1.6270 (estimate)
• Storage Temp.: room temp
• Solubility: Soluble in most solvents (U.S. EPA, 1985)
• Water Solubility: 14.4ug/L(20 oC)
• CAS DataBase Reference: AROCLOR 1260, 1X1ML, ISO, 1000UG/ML(CAS DataBase Reference)
• NIST Chemistry Reference: AROCLOR 1260, 1X1ML, ISO, 1000UG/ML(11096-82-5)
• EPA Substance Registry System: AROCLOR 1260, 1X1ML, ISO, 1000UG/ML(11096-82-5)

Safety Data

• Hazard Codes: F,N,Xn,T
• Statements: 11-23/24/25-39/23/24/25-67-65-62-51/53-48/20-38-50/53-33-52/53-45
• Safety Statements: 36/37-45-62-61-60-33-29-16-9-53
• RIDADR: 2315
• WGK Germany: 3
• HazardClass: 9
• PackingGroup: II
• Hazardous Substances Data: 11096-82-5(Hazardous Substances Data)

Usage

Description

AROCLOR 1260, 1X1ML, ISO, 1000UG/ML is a light-yellow, sticky, soft, nonflammable resin with a faint odor, characterized by its viscous oily liquid nature and approximately 6.3 chlorine atoms per molecule.

Uses

Used in Plastic Industry:
AROCLOR 1260, 1X1ML, ISO, 1000UG/ML is used as a secondary plasticizer for polyvinyl chloride, enhancing the flexibility and workability of the material.
Used in Fiberglass Industry:
AROCLOR 1260, 1X1ML, ISO, 1000UG/ML is used in polyester resins to increase the strength of fiberglass, providing improved mechanical properties and durability.
Used in Paint and Coating Industry:
AROCLOR 1260, 1X1ML, ISO, 1000UG/ML is used in varnish formulations to improve water and alkali resistance, offering better protection and longevity for coated surfaces.
Used in Electrical Industry:
AROCLOR 1260, 1X1ML, ISO, 1000UG/ML is used as an insulator fluid for electric condensers, ensuring effective insulation and preventing electrical failures.
Used in Lubricant Industry:
AROCLOR 1260, 1X1ML, ISO, 1000UG/ML is used as an additive in very high-pressure lubricants, enhancing their performance and reducing wear and tear.
Used in Insecticide Formulations:
AROCLOR 1260, 1X1ML, ISO, 1000UG/ML has been used in the past as an additive in chlordane and BHC insecticide formulations, increasing the effective kill-life of the insecticides.
Used in Wire and Cable Industry:
AROCLOR 1260, 1X1ML, ISO, 1000UG/ML is used in wire or cable coatings, providing insulation and protection against environmental factors.
Used in Insulation Materials:
AROCLOR 1260, 1X1ML, ISO, 1000UG/ML is used as an impregnant in cotton and asbestos braided insulation, enhancing the insulating properties and durability of the materials.
Used in Air Filtration Industry:
AROCLOR 1260, 1X1ML, ISO, 1000UG/ML is used in coating on glass air filter pads and metal mesh to filter air and gas streams, improving the efficiency of the filtration process.
Used in Lacquer Industry:
AROCLOR 1260, 1X1ML, ISO, 1000UG/ML is used in various nitrocellulose lacquers to impart weather resistance, luster, adhesion, and decreased burning rate, enhancing the performance and appearance of coated surfaces.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

Simple aromatic halogenated organic compounds are very unreactive. Reactivity generally decreases with increased degree of substitution of halogen for hydrogen atoms.

Health Hazard

ACUTE/CHRONIC HAZARDS: Toxic irritant. Hazardous decomposition products.

Fire Hazard

Some may burn but none ignite readily. Containers may explode when heated. Some may be transported hot.

Safety Profile

Confirmed carcinogen with carcinogenic and neoplastigenic data. Moderately toxic by ingestion and skin contact. Experimental reproductive effects. Mutation data reported. When heated to decomposition it emits highly toxic fumes of Cl-. Used in heat transfer, hydraulic fluids, lubricants, and insecticides. See also POLYCHLORINATED BIPHENYLS.

Environmental fate

Biological. 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-1260 was statically incubated in the dark at 25 °C with yeast extract and settled domestic wastewater inoculum, no significant biodegradation was observed (Tabak et al., 1981). Photolytic. PCB-1260 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. After 2 h, about 75% of the congeners were destroyed. Without sodium borohydride, only 10% of the congeners had reacted. Products identified by GC include biphenyl, 2-, 3- and 4- chlorobiphenyl, six dichlorobiphenyls, three trichlorobiphenyls, 1-phenyl-1,4-cyclohexadiene, and 1-phenyl-3-cyclohexene (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 21, 57, and 22 wt %, respectively. The catalyst used was zinc phthalocyanine (4.5 nM). When PCB-1260 (100 mg), the emulsion and catalyst were subjected to a current of mA/cm2 on 11.2 cm2 lead electrode for 18 h, a dechlorination yield of >99.8 % was achieved. Reaction products included minor amounts of mono- and dichlorobiphenyls (0.02 mg), biphenyl and reduced alkylbenzene derivatives.

InChI:InChI=1/C12H3Cl7/c13-4-1-5(14)9(6(15)2-4)10-7(16)3-8(17)11(18)12(10)19/h1-3H