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506052

Supelco

Iodmethan -Lösung

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

Synonym(e):

Methyliodid -Lösung

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About This Item

Empirische Formel (Hill-System):
CH3I
CAS-Nummer:
74-88-4
Molekulargewicht:
141.94
Beilstein:
969135
MDL-Nummer:
MFCD00001073
UNSPSC-Code:
12000000
PubChem Substanz-ID:
329757611

Qualität

certified reference material
TraceCERT®

Produktlinie

TraceCERT®

Analysenzertifikat (CofA)

current certificate can be downloaded

Leistungsmerkmale

standard type calibration

Verpackung

ampule of 1 mL

Konzentration

2000 μg/mL in methanol: water (4:1)

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

cleaning products
cosmetics
environmental
food and beverages
personal care

Format

single component solution

Lagertemp.

-10 to -25°C

SMILES String

CI

InChI

1S/CH3I/c1-2/h1H3

InChIKey

INQOMBQAUSQDDS-UHFFFAOYSA-N

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Anwendung

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

Sonstige Hinweise

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.

Rechtliche Hinweise

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

Signalwort

Danger

Gefahreneinstufungen

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

Zielorgane

Eyes,Central nervous system

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 2

Flammpunkt (°F)

50.0 °F - closed cup

Flammpunkt (°C)

10 °C - closed cup

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
LRAD7489
LRAC9014
LRAC4746
LRAB8981
XA26237V

Die passende Version wird nicht angezeigt?

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Suche nach COA

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Iodmethan-d3 ≥99.5 atom % D, ≥99% (CP), contains copper as stabilizer

Sigma-Aldrich

176036

Iodmethan-d3

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

Supelco

89143

Adipinsäure

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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