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176036

Sigma-Aldrich

Iodomethane-d3

≥99.5 atom % D, ≥99% (CP), contains copper as stabilizer

Synonym(s):

Deuterated iodomethane, Methyl-d3 Iodide

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About This Item

Linear Formula:
CD3I
CAS Number:
865-50-9
Molecular Weight:
144.96
Beilstein:
1732026
EC Number:
231-159-6
MDL number:
MFCD00001074
UNSPSC Code:
12142201
PubChem Substance ID:
24850545
NACRES:
NA.12

vapor density

4.89 (vs air)

vapor pressure

22.76 psi ( 55 °C)
6.61 psi ( 20 °C)

isotopic purity

≥99.5 atom % D

Assay

≥99% (CP)

form

liquid

contains

copper as stabilizer

refractive index

n20/D 1.5262 (lit.)

bp

42 °C (lit.)

mp

−66.5 °C (lit.)

density

2.329 g/mL at 25 °C

application(s)

environmental

mass shift

M+3

storage temp.

2-8°C

SMILES string

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

InChI

1S/CH3I/c1-2/h1H3/i1D3

InChI key

INQOMBQAUSQDDS-FIBGUPNXSA-N

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General description

CD3I is isotopically deuterium- enriched reagent of methyl iodide.

Packaging

This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.

accessory

Product No.
Description
Pricing

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

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Yunli Hu et al.
Rapid communications in mass spectrometry : RCM, 27(8), 865-877 (2013-03-16)
Mass spectrometry based comparative glycomics is essential for disease biomarker discovery. However, developing a reliable quantification method is still a challenging task. We here report an isotopic labeling strategy employing stable isotopic iodomethane for comparative glycomic profiling by liquid chromatography/electrospray
Xue Dong et al.
Analytical chemistry, 91(18), 11794-11802 (2019-07-30)
Glycosylation is an important post-translational modification of proteins. Many diseases, such as cancer, have proved to be related to aberrant glycosylation. High throughput quantitative methods have gained attention recently in the study of glycomics. With the development of high-resolution mass
Warayuth Sajomsang et al.
International journal of biological macromolecules, 50(1), 263-269 (2011-11-22)
Five water-soluble chitosan derivatives were carried out by quaternizing either iodomethane or N-(3-chloro-2-hydroxypropyl) trimethylammonium chloride (Quat188) as a quaternizing agent under basic condition. The degree of quaternization (DQ) ranged between 28±2% and 90±2%. The antifungal activity was evaluated by using
Azarmidokht Gholamipour-Shirazi et al.
Organic & biomolecular chemistry, 10(40), 8059-8063 (2012-09-15)
We describe here the determination of the alkylation rate of a set of organic superbases by iodomethane in DMF using a microfluidic continuous flow reactor. Surprisingly, log k(Alkylation) follows the inverse trend of pK(BH+) of the base. Mayr's equation allows
Edvard Ehler et al.
Neurotoxicology, 32(3), 307-311 (2011-02-19)
Dichloromethane and iodomethane are colorless relatively volatile liquids, which are used as solvents in chemical manufacturing processes. The major route of exposure is via inhalation and to a lesser extent through the skin and digestive tract. Both substances are characterized
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