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D122602

1,4-Diiodobutane

Name: 1,4-Diiodobutane
Brand: ALDRICH

≥99%, contains copper as stabilizer

Synonym(s):

Tetramethylene diiodide

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About This Item

Linear Formula:

I(CH₂)₄I

CAS Number:

628-21-7

Molecular Weight:

309.92

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24893380

EC Number:

211-032-1

Beilstein/REAXYS Number:

1098276

MDL number:

MFCD00001099

Assay:

≥99%

Form:

liquid

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Properties

Quality Level

100

assay

≥99%

form

liquid

contains

copper as stabilizer

refractive index

n20/D 1.621 (lit.)

bp

147-152 °C/26 mmHg (lit.)

mp

6 °C (lit.)

density

2.35 g/mL at 25 °C (lit.)

SMILES string

ICCCCI

InChI

1S/C4H8I2/c5-3-1-2-4-6/h1-4H2

InChI key

ROUYUBHVBIKMQO-UHFFFAOYSA-N

Description

Storage Class

10 - Combustible liquids

wgk

WGK 3

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

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Gas chromatographic determination of busulfan in plasma with electron-capture detection.

M Hassan et al.

Journal of chromatography, 277, 374-380 (1983-10-14)

Biliary excretion of a glutathione conjugate of busulfan and 1,4-diiodobutane in the rat.

D H Marchand et al.

Drug metabolism and disposition: the biological fate of chemicals, 16(1), 85-92 (1988-01-01)

gamma-Glutamyl-beta-(S-tetrahydrothiophenium)alanyl-glycine, the glutathione-sulfonium conjugate of busulfan and 1,4-diiodobutane, was identified in the bile of rats following intravenous administration of equimolar doses of either compound. The glutathione-sulfonium conjugate was synthesized from 1-bromo-4-chlorobutane and characterized by 1H and 13C NMR and FAB/MS.

Glutathione S-transferases catalyzed conjugation of 1,4-disubstituted butanes with glutathione in vitro.