Skip to Content
MilliporeSigma
All Photos(1)

Documents

D122602

Sigma-Aldrich

1,4-Diiodobutane

≥99%, contains copper as stabilizer

Synonym(s):

Tetramethylene diiodide

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
I(CH2)4I
CAS Number:
628-21-7
Molecular Weight:
309.92
Beilstein/REAXYS Number:
1098276
EC Number:
211-032-1
MDL number:
MFCD00001099
UNSPSC Code:
12352100
PubChem Substance ID:
24893380

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

Looking for similar products? Visit Product Comparison Guide

Related Categories

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 8

1 of 8

1,4-Dichlorobutane 99%

Sigma-Aldrich

D59100

1,4-Dichlorobutane

Hexadecafluoro-1,8-diiodooctane 98%

Sigma-Aldrich

484997

Hexadecafluoro-1,8-diiodooctane

1,6-Dibromohexane 96%

Sigma-Aldrich

D41007

1,6-Dibromohexane

4,4′-Diiodobiphenyl technical grade, 90%

Sigma-Aldrich

D122408

4,4′-Diiodobiphenyl

1,5-Dibromopentane 97%

Sigma-Aldrich

128007

1,5-Dibromopentane

1-Iodobutane 99%, contains copper as stabilizer

Sigma-Aldrich

167304

1-Iodobutane

Diiodomethane ReagentPlus®, 99%, contains copper as stabilizer

Sigma-Aldrich

158429

Diiodomethane

1,4-Diiodotetrafluorobenzene 98%

Sigma-Aldrich

282286

1,4-Diiodotetrafluorobenzene

D H Marchand et al.
Biochemical and biophysical research communications, 128(1), 360-367 (1985-04-16)
Rat liver glutathione S-transferases catalyzed the conjugation of 1,4-diiodobutane with glutathione in vitro. The reaction followed saturation kinetics and was dependent on the concentration of the enzyme, substrate and glutathione in the incubation media. S-Benzylglutathione inhibited the enzymatic conversion of
Gas chromatographic determination of busulfan in plasma with electron-capture detection.
M Hassan et al.
Journal of chromatography, 277, 374-380 (1983-10-14)
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.
Shimo Yu et al.
Polymers, 11(3) (2019-04-10)
Responsive polymer-based sensors have attracted considerable attention due to their ability to detect the presence of analytes and convert the detected signal into a physical and/or chemical change. High responsiveness, fast response speed, good linearity, strong stability, and small hysteresis
Ian C Watson et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 25(41), 9678-9690 (2019-05-16)
New N-heterocyclic olefins (NHOs) are described with functionalization on the ligand heterocyclic backbone and terminal alkylidene positions. Various PdII -NHO complexes have been formed and their use as pre-catalysts in Buchwald-Hartwig aminations was explored. The most active system for catalytic

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service