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637769

Sigma-Aldrich

4-Iodobiphenyl

97%

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About This Item

Linear Formula:
C6H5C6H4I
CAS Number:
1591-31-7
Molecular Weight:
280.10
EC Number:
216-469-1
MDL number:
MFCD00019028
UNSPSC Code:
12352100
PubChem Substance ID:
24882888
NACRES:
NA.22

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

Signal Word

Danger

Hazard Statements

H302,H318,H410

Hazard Classifications

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

637769-VAR:
637769-25G:4548173989648
637769-5G:4548173989655
637769-BULK:

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Certificates of Analysis (COA)

Lot/Batch Number
04329TE
05209PE
06518HC
06702BC
02517MB

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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
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

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