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D122602

Sigma-Aldrich

1,4-Diiodobutane

≥99%, contains copper as stabilizer

Synonym(s):

Tetramethylene diiodide

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About This Item

Linear Formula:
I(CH2)4I
CAS Number:
Molecular Weight:
309.92
Beilstein:
1098276
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

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

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Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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’.

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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)
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
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
Jianghong Cai et al.
Molecules (Basel, Switzerland), 25(20) (2020-10-18)
In comparison with pristine sinomenine and carborane precursors, the calculations of molecular docking with matrix metalloproteinases (MMPs) and methylcarboranyl-n-butyl sinomenine showed improved interactions. Accordingly, methylcarboranyl-n-butyl sinomenine shows a high potential in the treatment of rheumatoid arthritis (RA) in the presence

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