AROCLOR 1260, 1X1ML, ISO, 1000UG/ML
- Product Name
- AROCLOR 1260, 1X1ML, ISO, 1000UG/ML
- CAS No.
- 11096-82-5
- Chemical Name
- AROCLOR 1260, 1X1ML, ISO, 1000UG/ML
- Synonyms
- CLORPHENA60;Arclor 1260;Aroclor 1260;phenoclordp6;kanechlor600.;IRIDIUM STAND;aroclor1260(pcb);PCB Aroclor 1260;chlorodiphenyl(60%cl);aroclor 1260 solution
- CBNumber
- CB9498491
- Molecular Formula
- C12H4Cl6
- Formula Weight
- 360.87816
- MOL File
- 11096-82-5.mol
AROCLOR 1260, 1X1ML, ISO, 1000UG/ML Property
- Melting point:
- 115.76°C (estimate)
- Boiling point:
- 457.69°C (rough estimate)
- Density
- 1.5800 (estimate)
- vapor pressure
- 130.5 at 25 °C (estimated using GC retention data, Foreman and Bidleman, 1985)
- refractive index
- 1.6270 (estimate)
- Flash point:
- 11 °C
- storage temp.
- room temp
- solubility
- Soluble in most solvents (U.S. EPA, 1985)
- Water Solubility
- 14.4ug/L(20 ºC)
- Henry's Law Constant
- 0.244, 0.435, 0.754, 1.27, 2.10, 3.36, 5.27, 8.09, and 12.1 at 0.0, 5.0, 10.0, 15.0, 20.0, 25.0, 30.0, 35.5, and 40.0 °C, respectively (predicted, Burkhard et al., 1985)
- EPA Substance Registry System
- Aroclor 1260 (11096-82-5)
Safety
- Hazard Codes
- F,N,Xn,T
- Risk 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)
- Toxicity
- Suspected human carcinogen. Acute oral LD50 for rats 1,315 mg/kg (quoted, RTECS, 1985).
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Danger
- Hazard statements
-
H350May cause cancer
H373May cause damage to organs through prolonged or repeated exposure
- Precautionary statements
-
P202Do not handle until all safety precautions have been read and understood.
P260Do not breathe dust/fume/gas/mist/vapours/spray.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P308+P313IF exposed or concerned: Get medical advice/attention.
P405Store locked up.
P501Dispose of contents/container to..…
N-Bromosuccinimide Price
- Product number
- CRM48736
- Product name
- Aroclor 1260
- Purity
- certifiedreferencematerial,50?mg/kgintransformeroil,pkgof1×5?mL
- Packaging
- 1pkg
- Price
- $124
- Updated
- 2024/03/01
- Product number
- 48735
- Product name
- Aroclor 1260 solution
- Purity
- certified reference material, 500?mg/kg in transformer oil
- Packaging
- 5ml
- Price
- $165
- Updated
- 2024/03/01
- Product number
- 48704
- Product name
- Aroclor 1260 solution
- Purity
- certified reference material, 200?μg/mL in methanol
- Packaging
- 1mL
- Price
- $40.5
- Updated
- 2024/03/01
- Product number
- 44809
- Product name
- Aroclor 1260 solution
- Purity
- certified reference material, 1000?μg/mL in isooctane
- Packaging
- 1mL
- Price
- $49
- Updated
- 2024/03/01
AROCLOR 1260, 1X1ML, ISO, 1000UG/ML Chemical Properties,Usage,Production
Chemical Properties
Soft, sticky, light-yellow resin; approx- imately 6.3 chlorine atoms per molecule.
Physical properties
Light yellow, sticky, soft, nonflammable resin with a faint odor
Uses
Secondary plasticizer for polyvinyl chloride; in polyester resins to increase strength of
fiberglass; varnish formulations to improve water and alkali resistance; as an insulator fluid for
electric condensers and as an additive in very high pressure lubricants. In fluorescent and highintensity
discharge ballasts manufactured prior to 1979 (U.S. EPA, 1998).
Also used in wire or cable coatings; impregnants in cotton and asbestos braided insulation;
coating on glass air filter pads, metal mesh to filter air and gas streams (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 and in melt coatings
for paper and cloth. In various nitrocellulose lacquers to impart weather resistance, luster,
adhesion, and decreased burning rate. These lacquers may also contain dibutyl phthalate and/or
tricresyl phosphate. A typical paper lacquer may contain acetone, isobutyl acetate, ethanol, toluene
and up to 20 wt % PCB-1260 (Monsanto, 1960).
General Description
Viscous oily liquid.
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.
AROCLOR 1260, 1X1ML, ISO, 1000UG/ML Preparation Products And Raw materials
Raw materials
Preparation Products
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