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Merck

377023

Sigma-Aldrich

2-Iodopropane-d7

98 atom % D, contains copper as stabilizer

Sinónimos:

Isopropyl-d7 iodide

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About This Item

Fórmula lineal:
(CD3)2CDI
Número de CAS:
Peso molecular:
177.04
MDL number:
UNSPSC Code:
12142201
PubChem Substance ID:
NACRES:
NA.21

isotopic purity

98 atom % D

assay

99% (CP)

form

liquid

contains

copper as stabilizer

technique(s)

NMR: suitable

impurities

≤0.5% water
water

refractive index

n20/D 1.4925 (lit.)

bp

88-90 °C

density

1.774 g/mL at 25 °C (lit.)

mass shift

M+7

storage temp.

2-8°C

SMILES string

[2H]C([2H])([2H])C([2H])(I)C([2H])([2H])[2H]

InChI

1S/C3H7I/c1-3(2)4/h3H,1-2H3/i1D3,2D3,3D

InChI key

FMKOJHQHASLBPH-YYWVXINBSA-N

General description

2-Iodopropane-d7 is 2-iodopropane with all the hydrogen atoms substituted by deuterium. Its synthesis from 2-propanol-d8 has been reported.

Application

2-Iodopropane-d7 may be used in the preparation of deuterium labeled prenyldiphosphate and prenylcysteine derivatives, and 1-(isopentylsulfonyl)benzene-d7.

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pictograms

FlameExclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

107.6 °F - closed cup

flash_point_c

42.00 °C - closed cup


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Maya Kamao et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 859(2), 192-200 (2007-10-19)
Sensitive quantification method for fat-soluble vitamins in human breast milk by liquid chromatography-tandem mass spectrometry was developed. Vitamins A, D and E were extracted from 10.0 mL of breast milk after saponifying by basic condition. Vitamin K derivatives were extracted
Thangaiah Subramanian et al.
Journal of labelled compounds & radiopharmaceuticals, 56(8), 370-375 (2013-11-29)
A Wittig reaction employing Li(CD3)2CP(C6H5)3 was used to prepare d6-farnesol and d6-geranylgeraniol. Reductive amination of aniline-2,3,4,5,6-d5 was used to prepare the unnatural isoprenoid analogues d5-anilinogeraniol and d5-anilinofarnesol. All of these deuterated isoprenols were elaborated into their diphosphate and cysteine thioether
Chemistry of the 2, 5-didehydropyridine biradical: Computational, kinetic, and trapping studies toward drug design.
Hoffner J, et al.
Journal of the American Chemical Society, 120(2), 376-385 (1998)

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