377023
2-Iodopropane-d7
98 atom % D, contains copper as stabilizer
Synonym(s):
Isopropyl-d7 iodide
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About This Item
Linear Formula:
(CD3)2CDI
CAS Number:
Molecular Weight:
177.04
MDL number:
UNSPSC Code:
12142201
PubChem Substance ID:
NACRES:
NA.21
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isotopic purity
98 atom % D
Quality Level
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.[1]
Application
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Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Flam. Liq. 3
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
107.6 °F - closed cup
Flash Point(C)
42.00 °C - closed cup
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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)
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
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
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