176036

Sigma-Aldrich

Iodomethane-d3

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

Sinónimos:
Methyl-d3 Iodide, Deuterated iodomethane
Fórmula lineal:
CD3I
Número de CAS:
Peso molecular:
144.96
Beilstein/REAXYS Number:
1732026
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.12

Quality Level

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)

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

Featured Industry

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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Packaging

5, 25, 50 g in glass bottle
1 g in ampule
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

hazcat

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 Germany

WGK 3

Flash Point F

Not applicable

Flash Point C

Not applicable

Certificado de Análisis

Certificado de origen

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...
Rainer Glaser et al.
Journal of agricultural and food chemistry, 60(7), 1776-1787 (2012-02-09)
The results are reported of a theoretical study of iodomethane (H(3)C-I, 1) and chloropicrin (Cl(3)C-NO(2), 2), of the heterodimers 3-6 formed by aggregation of 1 and 2, and of their addition products 7 and 8 and their possible fragmentation reactions...
Nicole J Rijs et al.
Dalton transactions (Cambridge, England : 2003), 39(37), 8655-8662 (2010-08-18)
A combination of multistage mass spectrometry experiments and DFT calculations were used to examine the synthesis and reactivity of dimethylaurate. Collision induced dissociation (CID) of [(CH(3)CO(2))(4)Au](-) proceeded via reductive elimination of acetylperoxide to yield the diacetate [CH(3)CO(2)AuO(2)CCH(3)](-), which in turn...
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....

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