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637769

4-Iodobiphenyl

Name: 4-Iodobiphenyl
Brand: ALDRICH

97%

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About This Item

Linear Formula:

C₆H₅C₆H₄I

CAS Number:

1591-31-7

Molecular Weight:

280.10

NACRES:

NA.22

PubChem Substance ID:

24882888

UNSPSC Code:

12352100

EC Number:

216-469-1

MDL number:

MFCD00019028

Assay:

97%

Form:

solid

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Properties

Quality Level

100

assay

97%

form

solid

mp

110-114 °C

functional group

iodo, phenyl

SMILES string

Ic1ccc(cc1)-c2ccccc2

InChI

1S/C12H9I/c13-12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-9H

InChI key

NXYICUMSYKIABQ-UHFFFAOYSA-N

Description

pictograms

GHS05,GHS07,GHS09

signalword

Danger

hcodes

H302,H318,H410

pcodes

P264 - P273 - P280 - P301 + P312 - P305 + P351 + P338 - P391

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Biodehalogenation and metabolism of 125[I]-4-iodobiphenyl.

J E Sinsheimer et al.

Journal of pharmaceutical sciences, 70(5), 546-549 (1981-05-01)

[125I]-4-Iodobiphenyl has been used as a model compound to investigate the in vivo metabolism of iodinated aromatic compounds in the rat. Material balance studies showed that 57.6% of the injected dose was excreted via feces and 41.2% via urine. Distribution

Cytochrome P-450-mediated metabolism of biphenyl and the 4-halobiphenyls.

A Parkinson et al.

Biochemical pharmacology, 31(10), 1849-1856 (1982-05-15)

The in vitro metabolism of biphenyl, 4-fluoro-, 4-chloro-, 4-bromo- and 4-iodobiphenyl by cytochrome P-450-dependent monooxygenases was investigated using hepatic microsomes from immature male rats pretreated with phenobarbitone or 3-methylcholanthrene. The major route of metabolism of biphenyl and the 4-halobiphenyls was

Global Trade Item Number

SKU	GTIN
637769-25G	04061833390115
637769-5G	04061833356944