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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
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
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
Lifang Luo et al.
Journal of environmental quality, 40(1), 109-117 (2011-04-15)
Due to ever-increasing state and federal regulations, the future use of fumigants is predicted on reducing negative environmental impacts while offering sufficient pestcontrol efficacy. To foster the development of a best management practice, an integrated tool is needed to simultaneously
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