추천 제품
product name
Acetonitrile, anhydrous, 99.8%
Grade
anhydrous
Quality Level
vapor density
1.41 (vs air)
vapor pressure
72.8 mmHg ( 20 °C)
분석
99.8%
형태
liquid
autoignition temp.
973 °F
expl. lim.
16 %
기술
solid phase extraction (SPE): suitable
불순물
<0.001% water
<0.005% water (100 mL pkg)
증발 잔류물
<0.0005%
색상
colorless
refractive index
n20/D 1.344 (lit.)
bp
81-82 °C (lit.)
mp
−45 °C (lit.)
solubility
water: soluble (completely)
density
0.786 g/mL at 25 °C (lit.)
형식
neat
SMILES string
CC#N
InChI
1S/C2H3N/c1-2-3/h1H3
InChI key
WEVYAHXRMPXWCK-UHFFFAOYSA-N
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일반 설명
Acetonitrile, an aliphatic nitrile, is widely used as an organic solvent and intermediate in organic syntheses. It is transparent to UV-visible light, which makes it highly applicable in spectrophotometric and fluorimetric techniques. MeCN is utilized as a mobile phase component in many chromatographic techniques, due to its low viscosity, high elution strength and miscibility in water. It also plays a major role as an extractant medium in liquid-liquid extraction, solid-phase extraction or microextraction.
애플리케이션
Acetonitrile may be used as a solvent to prepare:
It may also be used as a reactant to synthesize:
- 1,2-Azidoalcohols and 1,2-azidoamines via cerium(III) chloride assisted ring opening of epoxides and aziridines by sodium azide.
- Cyano-bearing indolinones by oxidative arylalkylation of olefins in the presence of palladium catalyst.
It may also be used as a reactant to synthesize:
- Bis (diphenylphosphino) acetonitrile by reacting with n-butyllithium and then with chlorodiphenylphosphine.
- β-Acetamido ketones via coupling reaction with ketones or ketoesters and aldehydes in the presence of cobalt(II) chloride.
포장
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가격
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2
Storage Class Code
3 - Flammable liquids
WGK
WGK 2
Flash Point (°F)
35.6 °F - closed cup
Flash Point (°C)
2.0 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Bis (diphenylphosphino) acetonitrile: Synthesis, ligand properties and application in catalytic carbon?carbon coupling
Dalton Transactions, 14, 1409-1415 (2007)
Cobalt-catalysed three-component coupling involving ketones or ketoesters, aldehydes and acetonitrile: a novel one-pot synthesis of ?-acetamido ketones
Journal of the Chemical Society. Chemical Communications, 6, 713-714 (1994)
Concise Encyclopedia Chemistry, 56-56 (1994)
Cerium (III) chloride promoted highly regioselective ring opening of epoxides and aziridines using NaN3 in acetonitrile: a facile synthesis of 1,2-azidoalcohols and 1,2-azidoamines.
Organic Letters, 4(3), 343-345 (2002)
Palladium-Catalyzed Oxidative Arylalkylation of Activated Alkenes: Dual C-H Bond Cleavage of an Arene and Acetonitrile.
Angewandte Chemie (International Edition in English), 50(52), 12578-12581 (2011)
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