D122602
1,4-Diiodobutane
≥99%, contains copper as stabilizer
Sinónimos:
Tetramethylene diiodide
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About This Item
Fórmula lineal:
I(CH2)4I
Número de CAS:
Peso molecular:
309.92
Beilstein/REAXYS Number:
1098276
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Productos recomendados
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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Categorías relacionadas
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Los clientes también vieron
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.
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
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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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