176036
Iodomethane-d3
≥99.5 atom % D, ≥99% (CP), contains copper as stabilizer
동의어(들):
Deuterated iodomethane, Methyl-d3 Iodide
로그인조직 및 계약 가격 보기
모든 사진(4)
About This Item
Linear Formula:
CD3I
CAS Number:
Molecular Weight:
144.96
Beilstein:
1732026
EC Number:
MDL number:
UNSPSC 코드:
12142201
PubChem Substance ID:
NACRES:
NA.12
추천 제품
vapor density
4.89 (vs air)
Quality Level
vapor pressure
22.76 psi ( 55 °C)
6.61 psi ( 20 °C)
동위원소 순도
≥99.5 atom % D
분석
≥99% (CP)
양식
liquid
포함
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
응용 분야
environmental
pharmaceutical
질량 이동
M+3
저장 온도
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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일반 설명
CD3I is isotopically deuterium- enriched reagent of methyl iodide.
포장
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.
신호어
Danger
유해 및 위험 성명서
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
표적 기관
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
가장 최신 버전 중 하나를 선택하세요:
시험 성적서(COA)
Lot/Batch Number
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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