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5S06052

Supelco

Iodométhane

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

Synonyme(s) :

Iodométhane solution, Iodure de méthyle

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About This Item

Formule empirique (notation de Hill):
CH3I
Numéro CAS:
74-88-4
Poids moléculaire :
141.94
Numéro Beilstein :
969135
Numéro MDL:
MFCD00001073
Code UNSPSC :
77101502
ID de substance PubChem :
329758643

Qualité

analytical standard

Agence

EPA 8260

Description

Separate Source

Caractéristiques

standard type calibration

Conditionnement

ampule of 1 × 1 mL

Concentration

2000 μg/mL in methanol: water (4:1)

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

agriculture

Format

single component solution

Température de stockage

2-8°C

Chaîne SMILES 

CI

InChI

1S/CH3I/c1-2/h1H3

Clé InChI

INQOMBQAUSQDDS-UHFFFAOYSA-N

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Application

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

Pictogrammes

FlameSkull and crossbonesHealth hazard
GHS02,GHS06,GHS08

Mention d'avertissement

Danger

Classification des risques

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

Organes cibles

Eyes,Central nervous system

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

50.0 °F - closed cup

Point d'éclair (°C)

10 °C - closed cup

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves

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Certificats d'analyse (COA)

Lot/Batch Number
LC21924V
LC20843V
LC12558
LC09323
LC04882

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

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
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
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.
Nicole J Rijs et al.
Dalton transactions (Cambridge, England : 2003), 39(37), 8655-8662 (2010-08-18)
A combination of multistage mass spectrometry experiments and DFT calculations were used to examine the synthesis and reactivity of dimethylaurate. Collision induced dissociation (CID) of [(CH(3)CO(2))(4)Au](-) proceeded via reductive elimination of acetylperoxide to yield the diacetate [CH(3)CO(2)AuO(2)CCH(3)](-), which in turn
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.
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