176036
Iodomethane-d3
≥99.5 atom % D, ≥99% (CP), contains copper as stabilizer
Sinónimos:
Deuterated iodomethane, Methyl-d3 Iodide
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Fórmula lineal:
CD3I
Número CAS:
Peso molecular:
144.96
UNSPSC Code:
12142201
NACRES:
NA.12
PubChem Substance ID:
EC Number:
231-159-6
Beilstein/REAXYS Number:
1732026
MDL number:
Isotopic purity:
≥99.5 atom % D
Assay:
≥99% (CP)
Mass shift:
M+3
Form:
liquid
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Permítanos ayudarleInChI 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
Categorías relacionadas
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.
Application
- Mass spectrometry calibration
- Quality control reference standards
- Reaction mechanism investigation
Features and Benefits
Features
Benefits
- 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
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.
signalword
Danger
target_organs
Respiratory system
Clase de almacenamiento
6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
flash_point_f
Not applicable
flash_point_c
Not applicable
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Aquatic Acute 1 - Aquatic Chronic 2 - Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
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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
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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
Beata Jędrzejewska et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 79(5), 985-992 (2011-05-11)
Electronic absorption and fluorescence spectra of eight hemicyanine dyes were recorded at room temperature in several solvents of different polarity. The spectral data were analyzed using the theory of solvatochromism, based on a dielectric continuum description of the solvent and
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
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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