D157406
2-二甲氨基乙醇
别名:
N,N-二甲乙醇胺, N,N-二甲基-2-羟基乙胺, Jeffcat DMEA
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关于此项目
线性分子式:
(CH3)2NCH2CH2OH
化学文摘社编号:
分子量:
89.14
EC Number:
203-542-8
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1209235
MDL number:
signalword
Danger
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B - STOT SE 3
target_organs
Respiratory system
存储类别
3 - Flammable liquids
wgk
WGK 1
flash_point_f
104.0 °F - Seta closed cup
flash_point_c
40 °C - Seta closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Tadashi Tatsumi et al.
Bioorganic & medicinal chemistry, 18(7), 2720-2727 (2010-03-17)
Effects of retro-inverso (RI) modifications of HTLV-1 protease inhibitors containing a hydroxyethylamine isoster backbone were clarified. Construction of the isoster backbone was achieved by a stereoselective aldol reaction. Four diastereomers with different configurations at the isoster hydroxyl site and the
Olivier Blin et al.
Psychopharmacology, 207(2), 201-212 (2009-09-17)
Dimethylaminoethanol pyroglutamate (DMAE p-Glu) is a compound resulting from the reaction between dimethylaminoethanol (an indirect precursor of acetylcholine) and pyroglutamic acid (a cyclic derivative of glutamic acid having procholinergic properties and promnesic effects in both animals and man). The present
B Sommerfeld
Phytomedicine : international journal of phytotherapy and phytopharmacology, 14(11), 711-715 (2007-10-10)
Tricutan is a combination product of herbal extracts traditionally used for treatment of skin conditions, together with dimethylaminoethanol. The effectiveness of Tricutan in improving skin firmness and elasticity in photoaged facial skin was examined in a randomised, placebo-controlled, double-blind, split-face
Vera Sampels et al.
The Journal of biological chemistry, 287(20), 16289-16299 (2012-03-28)
The obligate intracellular and promiscuous protozoan parasite Toxoplasma gondii needs an extensive membrane biogenesis that must be satisfied irrespective of its host-cell milieu. We show that the synthesis of the major lipid in T. gondii, phosphatidylcholine (PtdCho), is initiated by
Ouassila Amiri-Attou et al.
Molecules (Basel, Switzerland), 10(3), 545-551 (2007-11-17)
We report herein the synthesis of substituted 2-(6-nitrobenzo[1,3]dioxol-5-yl)-1- aryl ethanols and 2-(6-nitrobenzo[1,3]dioxol-5-yl)-propionic acid ethyl esters from the reaction of 5-chloromethyl-6-nitrobenzo[1,3]dioxole with various aromatic carbonyl and alpha- carbonyl ester derivatives using the tetrakis(dimethylamino)ethylene (TDAE) methodology.
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