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07-4170

2-Dimethylaminoethanol

SAJ first grade, ≥99.0%

Synonym(s):

N,N-Dimethyl-2-hydroxyethylamine, N,N-Dimethylethanolamine, Jeffcat DMEA

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About This Item

Linear Formula:
(CH3)2NCH2CH2OH
CAS Number:
Molecular Weight:
89.14
EC Number:
203-542-8
UNSPSC Code:
12352104
PubChem Substance ID:
Beilstein/REAXYS Number:
1209235
MDL number:
Assay:
≥99.0%
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grade

SAJ first grade

vapor pressure

100 mmHg ( 55 °C), 6.12 mmHg ( 20 °C)

assay

≥99.0%

availability

available only in Japan

refractive index

n20/D 1.4294 (lit.)

bp

134-136 °C (lit.)

mp

−70 °C (lit.)

density

0.886 g/mL at 20 °C (lit.)

SMILES string

CN(C)CCO

InChI

1S/C4H11NO/c1-5(2)3-4-6/h6H,3-4H2,1-2H3

InChI key

UEEJHVSXFDXPFK-UHFFFAOYSA-N



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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

Storage Class

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



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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
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
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



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