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19-3510

Sigma-Aldrich

Iodomethane

SAJ first grade, ≥93.0%

Synonym(s):

Methyl iodide

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About This Item

Empirical Formula (Hill Notation):
CH3I
CAS Number:
Molecular Weight:
141.94
Beilstein/REAXYS Number:
969135
MDL number:
UNSPSC Code:
12352101
PubChem Substance ID:

grade

SAJ first grade

vapor density

4.89 (vs air)

vapor pressure

24.09 psi ( 55 °C)
7.89 psi ( 20 °C)

assay

≥93.0%

form

liquid

availability

available only in Japan

refractive index

n20/D 1.531 (lit.)

bp

41-43 °C (lit.)

mp

−64 (lit.)

density

2.28 g/mL at 25 °C (lit.)

SMILES string

CI

InChI

1S/CH3I/c1-2/h1H3

InChI key

INQOMBQAUSQDDS-UHFFFAOYSA-N

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signalword

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Aquatic Acute 1 - Aquatic Chronic 2 - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

89.8 °F - closed cup

flash_point_c

32.1 °C - closed cup


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R Otto et al.
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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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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
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)
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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