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12674-11-2

12674-11-2 Structure

12674-11-2 Structure
IdentificationBack Directory
[Name]

AROCLOR 1016, 1X5ML, TRANSFORMER OIL 50M G/KG
[CAS]

12674-11-2
[Synonyms]

PCB Aroclor 1016
aroclor 1016 solution
chlorodiphenyl(41%cl)
Aroclor 1016 (PCB 1016)
[40cfr136(1986)]pcb-1016
AROCLOR 1016, 50MG, NEAT
Arochlor 1016 in isooctane
Aroclor 1016 in Cyclohexane
Aroclor 1016@35 μg/mL in MeOH
Aroclor 1016@100 μg/mL in MeOH
Aroclor 1016 @1000 μg/mL in MeOH
Arochlor 1016 Solution in Hexane
Arochlor 1016 50mg [12674-11-2]
polychlorinated biphenyl mixture
Polychlorinated biphenyl (41% Cl)
Aroclor 1016@1000 μg/mL in Hexane
Aroclor 1016@35 μg/mL in Isooctane
AROCLOR 1016, 1X1ML, MEOH, 200UG/ML
AROCLOR 1016, 1X1ML, ISO, 1000UG/ML
polychlorinatedbiphenyl(aroclor1016)
AROCLOR 1016, 1X1ML, HEXANE 1000UG/ML
Aroclor 1016 @1000 μg/mL in Isooctane
Aroclor 1016@500 ppm in Transformer oil
PCB Aroclor 1016 @1000 μg/mL in Isooctane
Aroclor 1016@50 ppm w/w in Transformer oil
AROCLOR 1016, 1X5ML, TRANSFORMER OIL 50M G/KG
L20101600CY Aroclor 1016 10μg/mLin Cyclohexan
X20101600IO Aroclor 1016 100μg/mLin Isooctane
AROCLOR 1016, 1X5ML, TRANSFORMER OIL 500 MG/KG
aroclor 1016, 41perc.cl, pcb c12h8cl2 and c12h7cl3
ASTM Method D6160 Aroclor 1016 35 μg/mLin Methanol
Polychlorinated biphenyl (Aroclor 1016): (Chlorodiphenyl (41% Cl))
[Molecular Formula]

C12H7Cl3
[MDL Number]

MFCD01779887
[MOL File]

12674-11-2.mol
[Molecular Weight]

257.543
Chemical PropertiesBack Directory
[Melting point ]

63.91°C (estimate)
[Boiling point ]

333.69°C (rough estimate)
[density ]

1.3300 (estimate)
[vapor pressure ]

9.03 x 10-4 mmHg at 25 °C (estimated using GC retention data, Foreman and Bidleman, 1985)
[refractive index ]

1.6060 (estimate)
[Fp ]

-26 °C
[storage temp. ]

2-8°C
[solubility ]

Soluble in most solvents (U.S. EPA, 1985).
[Henry's Law Constant]

750 (Paris et al., 1978)
[Exposure limits]

Potential occupational carcinogen. NIOSH REL: TWA 1.0 μg/m3, IDLH 5 mg/m3.
[EPA Substance Registry System]

Aroclor 1016 (12674-11-2)
Safety DataBack Directory
[Hazard Codes ]

F,Xn,N,T,Xi
[Risk Statements ]

11-38-48/20-51/53-62-65-67-39/23/24/25-23/24/25-36/37/38-50/53-33-45
[Safety Statements ]

36/37-61-62-45-26-60-35-53-16
[RIDADR ]

2315
[WGK Germany ]

3
[RTECS ]

TQ1351000
[HazardClass ]

9
[PackingGroup ]

II
[Hazardous Substances Data]

12674-11-2(Hazardous Substances Data)
[Toxicity]

Drinking water standard (final): For all PCBs, the MCLG and MCL are zero and 0.5 μg/L, respectively (U.S. EPA, 2000).
Hazard InformationBack Directory
[Chemical Properties]

Viscous, oily, light yellow to pale yellow-brown liquid or white powder with a weak, characteristic odor
[Uses]

Insulator fluid for electric condensers; additive in high pressure lubricants. In fluorescent and high-intensity discharge ballasts manufactured prior to 1979 (U.S. EPA, 1998).
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 (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.
[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-1016 was statically incubated in the dark at 25 °C with yeast extract and settled domestic wastewater inoculum, no significant biodegradation was observed. At a concentration of 5 mg/L, percent losses after 7, 14, 21, and 28-d incubation periods were 44, 47, 46, and 48, respectively. At a concentration of 10 mg/L, only 22, 46, 20, and 13% losses were observed after the 7, 14, 21, and 28-d incubation periods, respectively (Tabak et al., 1981).
Chemical/Physical. PCB-1016 will not hydrolyze to any reasonable extent (Kollig, 1993).
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