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Sigma-Aldrich

Iodomethane

purum, ≥99.0% (GC)

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Synonym(s):
Methyl iodide
Empirical Formula (Hill Notation):
CH3I
CAS Number:
Molecular Weight:
141.94
Beilstein/REAXYS Number:
969135
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21

vapor density

4.89 (vs air)

Quality Level

vapor pressure

24.09 psi ( 55 °C)
7.89 psi ( 20 °C)

grade

purum

assay

≥99.0% (GC)

contains

silver wool as stabilizer

impurities

≤0.5% CH2I2

refractive index

n20/D 1.530
n20/D 1.531 (lit.)

bp

41-43 °C (lit.)
41-43 °C

mp

−64 (lit.)

solubility

water: soluble 14 g/L at 20 °C

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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General description

Iodomethane (Methyl iodide) is a colorless liquid. It can be prepared by reacting dimethyl sulfate with concentrated KI. Reaction of iodine and phosphorous with methanol has been reported to afford iodomethane. It reacts with tris(triphenylphosphine)chlororhodium(I) to afford the octahedral complex of rhodium(III), [RhlCl(CH3)(PPh3)2(ICH3)]. Kinetics of its reaction with atomic chlorine in the gas phase has been investigated. The absolute rate constant of the reaction has been reported.

Application

Iodomethane (Methyl iodide) may be employed in the preparation of stable neutral solutions of hypoiodous acid and various methyl esters.

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 Dam. 1 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

wgk_germany

WGK 3

ppe

Faceshields, Gloves, Goggles


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Farabi Temel
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This work designs the synthesis of a novel amino morpholine schiff base functionalized calix[4]arene cage (SCC), its deposition onto Quartz Crystal Microbalance (QCM) crystal surface, and usage for the selective detecting of formaldehyde (HCHO). The SCC modified QCM sensor has
Iodomethane oxidation by dimethyldioxirane: a new route to hypoiodous acid and iodohydrines.
Asensio G, et al.
Organic Letters, 1(13), 2125-2128 (1999)
Eagleson M.
Concise Encyclopedia Chemistry, 649-649 (1994)
Efficient methylation of carboxylic acids with potassium hydroxide/methyl sulfoxide and iodomethane.
Avila-Zarraga JG and Martinez R.
Synthetic Communications, 31(14), 2177-2183 (2001)
Interaction of tris (triphenylphosphine) chlororhodium (I) with iodomethane, methylallyl, and allyl chloride.
Lawson DN, et al.
J. Chem. Soc. Sect. A, 1733-1736 (1966)

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