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Merck

176036

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
UNSPSC Code:
12142201
NACRES:
NA.12
PubChem Substance ID:
24850545
EC Number:
231-159-6
Beilstein/REAXYS Number:
1732026
MDL number:
MFCD00001074

Key Documents

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Product Name

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

InChI key

INQOMBQAUSQDDS-FIBGUPNXSA-N

InChI

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

SMILES string

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

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
pharmaceutical

mass shift

M+3

storage temp.

2-8°C

Quality Level

100
200

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Related Categories

Application

  • Mass spectrometry calibration
  • Quality control reference standards
  • Reaction mechanism investigation

Features and Benefits

Features

  • Ideal for radiolabeling techniques
  • Enhances imaging contrast in biological studies
  • Supports Advanced drug delivery applications



Benefits

  • Enhances the effectiveness of imaging techniques
  • Provides valuable data for drug development
  • Improves the targeting of therapeutic agent

General description

Iodomethane-d3 ≥99.5 atom % D, ≥99% (CP), contains copper as stabilizer is a high-purity isotope product with a unique chemical profile that belongs to the class of isotopes. Produced by Sigma-Aldrich, we are committed to providing quality isotope products and a reliable supply chain. Available in industrial and pre-pack quantities.

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.

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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

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
MKCX4642
MKCX4641
MKCX4640
MKCX4289
MKCX4288

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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
Sarah J Feakins et al.
Rapid communications in mass spectrometry : RCM, 27(3), 430-436 (2013-01-03)
A published method to determine the hydrogen isotope ((2)H/(1)H) ratios of methoxyl groups, cleaved from lignin by hydroiodic acid (HI), calls for the analysis of methyl iodide (CH(3)I). However, analysis of halogenated compounds by gas chromatography/pyrolysis/isotope ratio mass spectrometry (GC/P/IRMS)
R Otto et al.
Nature chemistry, 4(7), 534-538 (2012-06-22)
Solvents have a profound influence on chemical reactions in solution and have long been used to control their outcome. Such effects are generally considered to be governed by thermodynamics; however, little is known about the steric effects of solvent molecules.
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
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