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추천 제품
생물학적 소스
synthetic
Quality Level
Grade
ACS reagent
vapor density
1.52 (vs air)
vapor pressure
14.63 psi ( 20 °C)
분석
≥99.5%
양식
liquid
autoignition temp.
365 °F
expl. lim.
60 %
불순물
≤0.008 meq/g Titr. acid
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일반 설명
Acetaldehyde is an industrially important solvent used as an intermediate for the synthesis of a wide range of compounds. On oxidation it forms acetic acid and ethanol on reduction.[1] The interaction of Criegee intermediate (CH2OO) with acetaldehyde has been measured.[2] Its effect as a neuroactive agent has been studied.[3] Alkynylation reaction of acetaldehyde by asymmetric catalysis has been reported.[4]
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Carc. 1B - Eye Irrit. 2 - Flam. Liq. 1 - Muta. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point (°F)
-38.0 °F - closed cup
Flash Point (°C)
-38.89 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves
이미 열람한 고객
Direct measurement of Criegee intermediate (CH2OO) reactions with acetone, acetaldehyde, and hexafluoroacetone.
Taatjes CA, et al.
Physical Chemistry Chemical Physics, 14(30), 10391-10400 (2012)
Proline-catalysed Mannich reactions of acetaldehyde.
Yang JW, et al.
Nature, 452(7186), 453-455 (2008)
Eagleson M.
Concise Encyclopedia Chemistry, 4-4 (1994)
One-pot cross double-Mannich reaction of acetaldehyde catalyzed by a binaphthyl-based amino sulfonamide.
Kano T, et al.
Chemical Communications (Cambridge, England), 49(11), 1118-1120 (2013)
Asymmetric Catalytic Alkynylation of Acetaldehyde: Application to the Synthesis of (+)-Tetrahydropyrenophorol.
Trost BM and Quintard A.
Angewandte Chemie (International Edition in English), 51(27), 6704-6708 (2012)
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