11096-82-5 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.
Check Digit Verification of cas no
The CAS Registry Mumber 11096-82-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,1,0,9 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 11096-82:
(7*1)+(6*1)+(5*0)+(4*9)+(3*6)+(2*8)+(1*2)=85
85 % 10 = 5
So 11096-82-5 is a valid CAS Registry Number.
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