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506052

Supelco

Iodomethane solution

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

Sinónimos:

Methyl iodide

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About This Item

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

grado

certified reference material
TraceCERT®

Línea del producto

TraceCERT®

CofA

current certificate can be downloaded

Características

standard type calibration

envase

ampule of 1 mL

concentración

2000 μg/mL in methanol: water (4:1)

técnicas

HPLC: suitable
gas chromatography (GC): suitable

aplicaciones

cleaning products
cosmetics
environmental
food and beverages
personal care

Formato

single component solution

temp. de almacenamiento

-10 to -25°C

cadena SMILES

CI

InChI

1S/CH3I/c1-2/h1H3

Clave InChI

INQOMBQAUSQDDS-UHFFFAOYSA-N

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Aplicación

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

Otras 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.

Información legal

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

Palabra de señalización

Danger

Clasificaciones de peligro

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

Órganos de actuación

Eyes,Central nervous system

Código de clase de almacenamiento

3 - Flammable liquids

Clase de riesgo para el agua (WGK)

WGK 2

Punto de inflamabilidad (°F)

50.0 °F - closed cup

Punto de inflamabilidad (°C)

10 °C - closed cup

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Certificados de análisis (COA)

Lot/Batch Number

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Christian R Evenhuis et al.
The journal of physical chemistry. A, 115(23), 5992-6001 (2011-02-12)
The photodissociation of methyl iodide in the A band is studied by full-dimensional (9D) wave packet dynamics calculations using the multiconfigurational time-dependent Hartree approach. The potential energy surfaces employed are based on the diabatic potentials of Xie et al. [J.
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.
Lifang Luo et al.
Environmental science & technology, 44(16), 6275-6280 (2010-08-14)
For fumigants, information on transport and fate as well as pest control is needed to develop management practices with the fewest negative environmental effects while offering sufficient pest control efficacy. For this purpose, a 2-D soil chamber with a surface-mounted
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
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