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506052

Supelco

Iodomethane solution

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

Sinonimo/i:

Methyl iodide

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About This Item

Formula empirica (notazione di Hill):
CH3I
Numero CAS:
74-88-4
Peso molecolare:
141.94
Beilstein:
969135
Numero MDL:
MFCD00001073
Codice UNSPSC:
12000000
ID PubChem:
329757611

Grado

certified reference material
TraceCERT®

Nome Commerciale

TraceCERT®

CdA

current certificate can be downloaded

Caratteristiche

standard type calibration

Confezionamento

ampule of 1 mL

Concentrazione

2000 μg/mL in methanol: water (4:1)

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

cleaning products
cosmetics
environmental
food and beverages
personal care

Formato

single component solution

Temperatura di conservazione

-10 to -25°C

Stringa SMILE

CI

InChI

1S/CH3I/c1-2/h1H3
INQOMBQAUSQDDS-UHFFFAOYSA-N

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Applicazioni

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

Altre note

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.

Note legali

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

Avvertenze

Danger

Indicazioni di pericolo

H225,H301 + H311 + H331,H370

Classi di pericolo

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

Organi bersaglio

Eyes,Central nervous system

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

50.0 °F - closed cup

Punto d’infiammabilità (°C)

10 °C - closed cup

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Certificati d'analisi (COA)

Lot/Batch Number
LRAD7489
LRAC9014
LRAC4746
LRAB8981
XA26237V

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Adipic acid certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

Supelco

89143

Adipic acid

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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