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D122408

4,4′-Diiodobiphenyl

Name: 4,4′-Diiodobiphenyl
Brand: ALDRICH

technical grade, 90%

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About This Item

Linear Formula:

IC₆H₄C₆H₄I

CAS Number:

3001-15-8

Molecular Weight:

406.00

NACRES:

NA.22

PubChem Substance ID:

24893379

UNSPSC Code:

12352100

EC Number:

221-080-5

MDL number:

MFCD00001057

Assay:

90%

Form:

powder

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Properties

grade

technical grade

Quality Level

100

assay

90%

form

powder

mp

201-204 °C (lit.)

SMILES string

Ic1ccc(cc1)-c2ccc(I)cc2

InChI

1S/C12H8I2/c13-11-5-1-9(2-6-11)10-3-7-12(14)8-4-10/h1-8H

InChI key

GPYDMVZCPRONLW-UHFFFAOYSA-N

Description

pictograms

GHS07

signalword

Warning

hcodes

H302 + H312 + H332

pcodes

P261 - P264 - P280 - P301 + P312 - P302 + P352 + P312 - P304 + P340 + P312

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

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

Regulatory Information

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Modulation at a cellular level of the thyroid hormone receptor-mediated gene expression by 1,2,5,6,9,10-hexabromocyclododecane (HBCD), 4,4'-diiodobiphenyl (DIB), and nitrofen (NIP).

Toshiko Yamada-Okabe et al.

Toxicology letters, 155(1), 127-133 (2004-12-09)

Previously, we demonstrated that some endocrine disrupting chemicals affected thyroid hormone receptor (TR)-mediated gene expression in HeLaTR cells that stably expressed the human TRalpha1. To examine whether widely used brominated flame retardants and pesticides affect TR-mediated gene expression, those with

Conformational Tuning of the Intramolecular Electronic Coupling in Molecular-Wire Biruthenium Complexes Bridged by Biphenyl Derivatives.

Dan-Dan Kong et al.

Chemistry (Weinheim an der Bergstrasse, Germany), 21(27), 9895-9904 (2015-05-28)

The synthesis and characterization of a series of biphenyl-derived binuclear ruthenium complexes with terminal {RuCl(CO)(PMe3)3} moieties and different structural arrangements of the phenyl rings are reported. Electrochemical studies revealed that the two metal centers of the binuclear ruthenium complexes interact

Induction of drug metabolism enzymes by dihalogenated biphenyls.

L van Bree et al.

Journal of biochemical toxicology, 5(1), 57-63 (1990-01-01)

The effects of pretreatment with symmetrically dihalogenated biphenyls (DXBs, X-F, Cl(C), Br(B) and I) on rat liver drug metabolism enzymes were investigated. 4,4'-DFB, -DCB, and -DBB as well as 2,2'-DFB appeared to be inducers of microsomal cytochrome P-450-linked monoxygenases (N-demethylases

Global Trade Item Number

SKU	GTIN
D122408-25G	04061833559024