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506052

Supelco

Iodomethane solution

certified reference material, 2000 μg/mL in methanol: water (4:1)

Sinônimo(s):

Methyl iodide

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About This Item

Fórmula empírica (Notação de Hill):
CH3I
Número CAS:
74-88-4
Peso molecular:
141.94
Beilstein:
969135
Número MDL:
MFCD00001073
Código UNSPSC:
12000000
ID de substância PubChem:
329757611

grau

certified reference material
TraceCERT®

linha de produto

TraceCERT®

Certificado de análise (CofA)

current certificate can be downloaded

Características

standard type calibration

embalagem

ampule of 1 mL

concentração

2000 μg/mL in methanol: water (4:1)

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

aplicação(ões)

cleaning products
cosmetics
environmental
food and beverages
personal care

formato

single component solution

temperatura de armazenamento

-10 to -25°C

cadeia de caracteres SMILES

CI

InChI

1S/CH3I/c1-2/h1H3

chave InChI

INQOMBQAUSQDDS-UHFFFAOYSA-N

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Aplicação

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Outras notas

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Informações legais

TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany

Palavra indicadora

Danger

Classificações de perigo

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

Órgãos-alvo

Eyes,Central nervous system

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

50.0 °F - closed cup

Ponto de fulgor (°C)

10 °C - closed cup

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
LRAD7489
LRAC9014
LRAC4746
LRAB8981
XA26237V

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Se precisar de uma versão específica, você pode procurar um certificado específico pelo número do lote ou da remessa.

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2-Iodopropane (stabilised) for synthesis

Sigma-Aldrich

8.43955

2-Iodopropane

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.
Microhydration effects on the intermediates of the S(N)2 reaction of iodide anion with methyl iodide.
Keisuke Doi et al.
Angewandte Chemie (International ed. in English), 52(16), 4380-4383 (2013-01-31)
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
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
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
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