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D122408

Sigma-Aldrich

4,4′-Diiodobiphenyl

technical grade, 90%

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25 G
€29.70

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25 G
€29.70

About This Item

Linear Formula:
IC6H4C6H4I
CAS Number:
3001-15-8
Molecular Weight:
406.00
EC Number:
221-080-5
MDL number:
MFCD00001057
UNSPSC Code:
12352100
PubChem Substance ID:
24893379
NACRES:
NA.22

€29.70

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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

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302 + H312 + H332

Hazard Classifications

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

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCD4925
MKBR4125V
08629PF
08512KU
07325JY

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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
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
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

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