AROCLOR 1260, 1X1ML, ISO, 1000UG/ML

Bezeichnung:AROCLOR 1260, 1X1ML, ISO, 1000UG/ML

CAS-Nr11096-82-5

Englisch Name:AROCLOR 1260, 1X1ML, ISO, 1000UG/ML

CBNumberCB9498491

SummenformelC12H4Cl6

Molgewicht360.87816

MOL-Datei11096-82-5.mol

AROCLOR 1260, 1X1ML, ISO, 1000UG/ML physikalisch-chemischer Eigenschaften

Schmelzpunkt	115.76°C (estimate)
Siedepunkt	457.69°C (rough estimate)
Dichte	1.5800 (estimate)
Dampfdruck	130.5 at 25 °C (estimated using GC retention data, Foreman and Bidleman, 1985)
Brechungsindex	1.6270 (estimate)
Flammpunkt	11 °C
storage temp.	room temp
Löslichkeit	Soluble in most solvents (U.S. EPA, 1985)
Wasserlöslichkeit	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 chemische Informationen	Aroclor 1260 (11096-82-5)

Sicherheit

Kennzeichnung gefährlicher	F,N,Xn,T
R-Sätze:	11-23/24/25-39/23/24/25-67-65-62-51/53-48/20-38-50/53-33-52/53-45
S-Sätze:	36/37-45-62-61-60-33-29-16-9-53
RIDADR	2315
WGK Germany	3
HazardClass	9
PackingGroup	II
Giftige Stoffe Daten	11096-82-5(Hazardous Substances Data)
Toxizität	Suspected human carcinogen. Acute oral LD50 for rats 1,315 mg/kg (quoted, RTECS, 1985).

Gefahreninformationscode (GHS)

AROCLOR 1260, 1X1ML, ISO, 1000UG/ML Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:
R11:Leichtentzündlich.
R23/24/25:Giftig beim Einatmen, Verschlucken und Berührung mit der Haut.
R39/23/24/25:Giftig: ernste Gefahr irreversiblen Schadens durch Einatmen, Berührung mit der Haut und durch Verschlucken.
R67:Dämpfe können Schläfrigkeit und Benommenheit verursachen.
R65:Gesundheitsschädlich: kann beim Verschlucken Lungenschäden verursachen.
R62:Kann möglicherweise die Fortpflanzungsfähigkeit beeinträchtigen.
R51/53:Giftig für Wasserorganismen, kann in Gewässern längerfristig schädliche Wirkungen haben.
R48/20:Gesundheitsschädlich: Gefahr ernster Gesundheitsschäden bei längerer Exposition durch Einatmen.
R38:Reizt die Haut.
R50/53:Sehr giftig für Wasserorganismen, kann in Gewässern längerfristig schädliche Wirkungen haben.
S-Sätze Betriebsanweisung:
S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn möglich, dieses Etikett vorzeigen).
S62:Bei Verschlucken kein Erbrechen herbeiführen. Sofort ärztlichen Rat einholen und Verpackung oder dieses Etikett vorzeigen.
S61:Freisetzung in die Umwelt vermeiden. Besondere Anweisungen einholen/Sicherheitsdatenblatt zu Rate ziehen.
S60:Dieses Produkt und sein Behälter sind als gefährlicher Abfall zu entsorgen.
S33:Maßnahmen gegen elektrostatische Aufladungen treffen.
S29:Nicht in die Kanalisation gelangen lassen.
S16:Von Zündquellen fernhalten - Nicht rauchen.
S9:Behälter an einem gut gelüfteten Ort aufbewahren.
Chemische Eigenschaften
Soft, sticky, light-yellow resin; approx- imately 6.3 chlorine atoms per molecule.
Physikalische Eigenschaften
Light yellow, sticky, soft, nonflammable resin with a faint odor
Verwenden
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).
Allgemeine Beschreibung
Viscous oily liquid.
Air & Water Reaktionen
Insoluble in water.
Reaktivität anzeigen
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.
Brandgefahr
Some may burn but none ignite readily. Containers may explode when heated. Some may be transported hot.
Sicherheitsprofil
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 Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

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