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Documenti fondamentali

148547

4,4′-PCB

98%

Sinonimo/i:

4.4′-Dichlorobiphenyl

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About This Item

Formula empirica (notazione di Hill):
C12H8Cl2
Numero CAS:
Peso molecolare:
223.10
Numero CE:
ID PubChem:
Prezzi e disponibilità al momento non sono disponibili

Saggio

98%

InChI

1S/C12H8Cl2/c13-11-5-1-9(2-6-11)10-3-7-12(14)8-4-10/h1-8H
YTBRNEUEFCNVHC-UHFFFAOYSA-N

Pittogrammi

Health hazardEnvironment

Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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Lot/Batch Number

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M T Scott et al.
Journal of pharmaceutical sciences, 73(8), 1171-1172 (1984-08-01)
A reverse-phase HPLC system was used for the determination of inorganic chloride liberated in vivo from two biphenyl compounds in the rat. Oral administration of [4-36Cl]chlorobiphenyl resulted in a total yield of 27.6% of the original dose excreted over 10
L van Bree et al.
Toxicology, 42(2-3), 259-274 (1986-12-15)
Both 4,4'-dichlorobiphenyl (4,4'-DCB) and 3-methylcholanthrene (3-MC) caused a substantial increase of phenacetin-induced hepatic glutathione (GSH) depletion, whereas phenobarbital (PB) had no effect, suggesting that 4,4'-DCB possesses cytochrome P-448 inducing activity. The O-deethylation of phenacetin by liver microsomes from control and
P Adriaens et al.
Applied and environmental microbiology, 55(4), 887-892 (1989-04-01)
Acinetobacter sp. strain 4CB1 was isolated from a polychlorobiphenyl-contaminated soil sample by using 4-chlorobenzoate as a sole source of carbon and energy. Resting cells of Acinetobacter sp. strain 4CB1 hydrolytically dehalogenated 4-chlorobenzoate under aerobic and anaerobic conditions, but 4-hydroxybenzoate accumulated
D Dietrich et al.
Applied and environmental microbiology, 61(11), 3904-3909 (1995-11-01)
The white rot fungus Phanerochaete chrysosporium has demonstrated abilities to degrade many xenobiotic chemicals. In this study, the degradation of three model polychlorinated biphenyl (PCB) congeners (4,4'-dichlorobiphenyl [DCB], 3,3',4,4'-tetrachlorobiphenyl, and 2,2',4,4',5,5'-hexachlorobiphenyl) by P. chrysosporium in liquid culture was examined. After
L van Bree et al.
The Journal of pharmacy and pharmacology, 41(5), 343-345 (1989-05-01)
The role of enzyme induction in the reduction by acetylsalicylic acid (ASA) of paracetamol-induced hepatic glutathione (GSH) depletion has been studied in rats. Administration of an overdose of paracetamol to control rats resulted in an appreciable decrease of GSH concentration.

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