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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%
Pricing and availability is not currently available.
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


