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经验公式(希尔记法):
CH3I
化学文摘社编号:
分子量:
141.94
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
200-819-5
MDL number:
Beilstein/REAXYS Number:
969135
Assay:
99.5%
Bp:
41-43 °C (lit.)
Vapor pressure:
24.09 psi ( 55 °C)
7.89 psi ( 20 °C)
7.89 psi ( 20 °C)
产品名称
碘甲烷, contains copper as stabilizer, ReagentPlus®, 99.5%
InChI key
INQOMBQAUSQDDS-UHFFFAOYSA-N
InChI
1S/CH3I/c1-2/h1H3
SMILES string
CI
vapor density
4.89 (vs air)
vapor pressure
24.09 psi ( 55 °C)
7.89 psi ( 20 °C)
product line
ReagentPlus®
assay
99.5%
form
liquid
contains
copper as stabilizer
dilution
(for general lab use)
refractive index
n20/D 1.531 (lit.)
bp
41-43 °C (lit.)
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
storage temp.
2-8°C
Quality Level
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Application
碘甲烷作为甲基化剂用于合成:
- N,N -十二烷基,甲基聚乙烯亚胺 (PEI),一种具有潜在应用前景的杀菌聚合物在杀菌涂料中的应用。
- 甲基化的吡啶衍生物,可用作活细胞成像的 RNA 特异性荧光探针。
General description
碘甲烷是一种常用作甲基化剂的卤代烷烃。
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
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
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
89.8 °F - closed cup
flash_point_c
32.1 °C - closed cup
ppe
Faceshields, Gloves, Goggles
法规信息
危险化学品
此项目有
Preparation, application and testing of permanent antibacterial and antiviral coatings
Haldar J, et al
Nature Protocols, 2(10), 2412-2412 (2007)
A protocol for preparing, characterizing and using three RNA-specific, live cell imaging probes: E36, E144 and F22
Li Q & Chang YT
Nature Protocols, 1(6), 2922-2922 (2006)
Interaction of tris (triphenylphosphine) chlororhodium (I) with iodomethane, methylallyl, and allyl chloride.
Lawson DN, et al.
J. Chem. Soc. Sect. A, 1733-1736 (1966)
Eagleson M.
Concise Encyclopedia Chemistry, 649-649 (1994)
Iodomethane oxidation by dimethyldioxirane: a new route to hypoiodous acid and iodohydrines.
Asensio G, et al.
Organic Letters, 1(13), 2125-2128 (1999)
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