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Fórmula empírica (notación de Hill):
CH3I
Número CAS:
Peso molecular:
141.94
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
200-819-5
MDL number:
Beilstein/REAXYS Number:
969135
Assay:
≥99.0% (GC)
Servicio técnico
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Permítanos ayudarleNombre del producto
Iodomethane, purum, ≥99.0% (GC)
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
mp
−64 (lit.)
solubility
water: soluble 14 g/L at 20 °C
density
2.28 g/mL at 25 °C (lit.)
functional group
alkyl halide, iodo
SMILES string
CI
InChI
1S/CH3I/c1-2/h1H3
InChI key
INQOMBQAUSQDDS-UHFFFAOYSA-N
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
target_organs
Respiratory system
Clase de almacenamiento
3 - Flammable liquids
flash_point_f
89.8 °F - closed cup
flash_point_c
32.1 °C - closed cup
ppe
Faceshields, Gloves, Goggles
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Eye Dam. 1 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
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Interaction of tris (triphenylphosphine) chlororhodium (I) with iodomethane, methylallyl, and allyl chloride.
Lawson DN, et al.
J. Chem. Soc. Sect. A, 1733-1736 (1966)
Iodomethane oxidation by dimethyldioxirane: a new route to hypoiodous acid and iodohydrines.
Asensio G, et al.
Organic Letters, 1(13), 2125-2128 (1999)




