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Merck
CN

5S06052

Iodomethane

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

Synonym(s):

Iodomethane solution, Methyl iodide

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About This Item

Empirical Formula (Hill Notation):
CH3I
CAS Number:
74-88-4
Molecular Weight:
141.94
PubChem Substance ID:
329758643
UNSPSC Code:
77101502
Beilstein/REAXYS Number:
969135
MDL number:
MFCD00001073

Key Documents

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Product Name

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

SMILES string

CI

InChI key

INQOMBQAUSQDDS-UHFFFAOYSA-N

InChI

1S/CH3I/c1-2/h1H3

grade

analytical standard

agency

EPA 8260

description

Separate Source

feature

standard type calibration

packaging

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

storage temp.

2-8°C

Quality Level

100

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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.

signalword

Danger

Hazard Classifications

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

target_organs

Eyes,Central nervous system

Storage Class

3 - Flammable liquids

wgk

WGK 2

flash_point_f

50.0 °F - closed cup

flash_point_c

10 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
LC21924V
LC20843V
LC12558
LC09323
LC04882

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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)
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
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
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
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