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5S06052

Supelco

Iodmethan

2000 μg/mL in methanol: water (4:1), analytical standard

Synonym(e):

Iodmethan -Lösung, 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:
77101502
PubChem Substanz-ID:
329758643

Qualität

analytical standard

Agentur

EPA 8260

Beschreibung

Separate Source

Leistungsmerkmale

standard type calibration

Verpackung

ampule of 1 × 1 mL

Konzentration

2000 μg/mL in methanol: water (4:1)

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

agriculture

Format

single component solution

Lagertemp.

2-8°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.

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

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves

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Analysenzertifikate (COA)

Lot/Batch Number
LC21924V
LC20843V
LC12558
LC09323
LC04882

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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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