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176036

Sigma-Aldrich

Iodomethane-d3

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

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Synonym(s):
Deuterated iodomethane, Methyl-d3 Iodide
Linear Formula:
CD3I
CAS Number:
Molecular Weight:
144.96
Beilstein/REAXYS Number:
1732026
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.12

vapor density

4.89 (vs air)

Quality Level

100
200

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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1 of 4

This Item
296759492825492833
Iodomethane-d3 ≥99.5 atom % D, ≥99% (CP), contains copper as stabilizer

176036

Iodomethane-d3

Iodomethane-12C,d3 99.9 atom % 12C, 98 atom % D, 99% (CP), contains copper as stabilizer

296759

Iodomethane-12C,d3

Iodomethane-d ≥98 atom % D, ≥99% (CP), contains copper as stabilizer

492825

Iodomethane-d

Iodomethane-d2 ≥98 atom % D, ≥99% (CP), contains copper as stabilizer

492833

Iodomethane-d2

mass shift

M+3

mass shift

M+3

mass shift

M+1

mass shift

M+2

isotopic purity

≥99.5 atom % D

isotopic purity

99.9 atom % 12C, 98 atom % D

isotopic purity

≥98 atom % D

isotopic purity

≥98 atom % D

form

liquid

form

-

form

-

form

-

refractive index

n20/D 1.5262 (lit.)

refractive index

-

refractive index

n20/D 1.526 (lit.)

refractive index

n20/D 1.526 (lit.)

bp

42 °C (lit.)

bp

42 °C (lit.)

bp

42 °C (lit.)

bp

42 °C (lit.)

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

signalword

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

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

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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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
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
Kazunori Kawamura et al.
Nuclear medicine and biology, 39(1), 89-99 (2011-08-13)
To explore the possible use of positron emission tomography (PET) probes for imaging of I(2)-imidazoline receptors (I(2)Rs) in peripheral tissues, we labeled two new I(2)R ligands, 2-[2-(o-tolyl)vinyl]-4,5-dihydro-1H-imidazole (K(i) for I(2)Rs, 3.7 nM) and 2-[2-(o-tolyl)ethyl]-4,5-dihydro-1H-imidazole (K(i) for I(2)Rs, 1.7 nM) with
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
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

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