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Details

Stereochemistry ABSOLUTE
Molecular Formula C4H11NO.C4H6O6
Molecular Weight 239.2231
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DEANOL BITARTRATE

SMILES

CN(C)CCO.O[C@H]([C@@H](O)C(O)=O)C(O)=O

InChI

InChIKey=UIEGYKVRCKDVKQ-LREBCSMRSA-N
InChI=1S/C4H11NO.C4H6O6/c1-5(2)3-4-6;5-1(3(7)8)2(6)4(9)10/h6H,3-4H2,1-2H3;1-2,5-6H,(H,7,8)(H,9,10)/t;1-,2-/m.1/s1

HIDE SMILES / InChI

Molecular Formula C4H6O6
Molecular Weight 150.0868
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula C4H11NO
Molecular Weight 89.1362
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

DEANOL is an inactive component of CERAVE® hydrocortisone anti-itch cream, which is used for temporarily relieve itching associated with minor skin irritations, inflammation, and rashes due to eczema, soaps, detergents, cosmetics, seborrheic dermatitis, psoriasis. DEANOL is also used as a food additive.

Approval Year

Doses

Doses

DosePopulationAdverse events​
0.1 % single, topical
Highest studied dose
healthy
6000 mg 1 times / day multiple, oral
Highest studied dose
Dose: 6000 mg, 1 times / day
Route: oral
Route: multiple
Dose: 6000 mg, 1 times / day
Sources: Page: p.188
unhealthy
Health Status: unhealthy
Condition: Involuntary movement disorders
Sources: Page: p.188
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
Inhibitors of choline uptake and metabolism cause developmental abnormalities in neurulating mouse embryos.
2001 Aug
Studies of the side chain cleavage of deramciclane in rats with radiolabelled compounds.
2002 Mar
Reactivity and molecular recognition: amine methylation by an introverted ester.
2003 Dec 3
Efficacy of dimethylaminoethanol (DMAE) containing vitamin-mineral drug combination on EEG patterns in the presence of different emotional states.
2003 May 30
The sea urchin embryo as a model for mammalian developmental neurotoxicity: ontogenesis of the high-affinity choline transporter and its role in cholinergic trophic activity.
2003 Nov
[11C]Choline as a PET biomarker for assessment of prostate cancer tumor models.
2004 Jun 1
A new design strategy for dispersion stabilization of Ni particles based on the surface acid and base properties of Ni particles.
2007 Aug 15
The antiwrinkle effect of topical concentrated 2-dimethylaminoethanol involves a vacuolar cytopathology.
2007 Mar
Mannosylated poly(ethylene oxide)-b-poly(epsilon-caprolactone) diblock copolymers: synthesis, characterization, and interaction with a bacterial lectin.
2007 Sep
Bis[N-(2-hydroxy-ethyl)-N-methyl-glycinato]copper(II).
2008 Nov 22
Quantitative determination of dimethylaminoethanol in cosmetic formulations by nuclear magnetic resonance spectroscopy.
2008 Nov-Dec
Organocadmium aminoalcoholates: synthesis, structure, and materials chemistry.
2008 Oct 20
Effects of dimethylaminoethanol pyroglutamate (DMAE p-Glu) against memory deficits induced by scopolamine: evidence from preclinical and clinical studies.
2009 Dec
Mitochondrial 2,4-dienoyl-CoA reductase deficiency in mice results in severe hypoglycemia with stress intolerance and unimpaired ketogenesis.
2009 Jul
The pentameric vertex proteins are necessary for the icosahedral carboxysome shell to function as a CO2 leakage barrier.
2009 Oct 21
Application of high performance liquid chromatography coupled to on-line solid-phase extraction-nuclear magnetic resonance spectroscopy for the analysis of degradation products of V-class nerve agents and nitrogen mustard.
2010 Apr 23
Mesotherapy - The french connection.
2010 Jan
Chloridotris[μ(2)-2-(dimethyl-amino)-ethano-lato]-μ(3)-hydroxido-tri-μ(2)-trifluoro-acetato-tetra-copper(II) tetra-hydro-furan solvate.
2010 Jun 18
In vitro cytotoxicity of benzopyranone derivatives with basic side chain against human lung cell lines.
2010 Nov
Reduced dimethylaminoethanol in [(18)F]fluoromethylcholine: an important step towards enhanced tumour visualization.
2010 Nov
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:21:29 GMT 2023
Edited
by admin
on Fri Dec 15 15:21:29 GMT 2023
Record UNII
D240J05W14
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DEANOL BITARTRATE
MI   WHO-DD  
Common Name English
ETHANOL, 2-(DIMETHYLAMINO)-, (2R,3R)-2,3-DIHYDROXYBUTANEDIOATE (1:1)
Systematic Name English
DIMETHYLAMINOETHANOL TARTRATE [INCI]
Common Name English
DIMETHYLAMINOETHYL BITARTRATE
Systematic Name English
ETHANOL, 2-(DIMETHYLAMINO)-, (2R, 3R)-2,3-DIHYDROXYBUTANEDIOATE (SALT)
Common Name English
ORISTAR DMAE TARTRATE
Brand Name English
DEANOL TARTRATE
Common Name English
DMAE TARTRATE
Common Name English
DMAE L-TARTRATE
Brand Name English
DIMETHYLAMINOETHANOL TARTRATE
INCI  
INCI  
Official Name English
Deanol bitartrate [WHO-DD]
Common Name English
DIMETHYLAMINOETHANOL BITARTRATE
Systematic Name English
DEANOL BITARTRATE [MI]
Common Name English
N,N-DIMETHYLETHANOLAMINE-TARTARIC ACID SALT
Common Name English
2-DIMETHYLAMINOETHANOL TARTRATE
Systematic Name English
2-(DIMETHYLAMINO)ETHANOL BITARTRATE
Systematic Name English
DMAE BITARTRATE
Common Name English
Classification Tree Code System Code
CFR 21 CFR 331.15
Created by admin on Fri Dec 15 15:21:30 GMT 2023 , Edited by admin on Fri Dec 15 15:21:30 GMT 2023
CFR 21 CFR 331.11
Created by admin on Fri Dec 15 15:21:30 GMT 2023 , Edited by admin on Fri Dec 15 15:21:30 GMT 2023
Code System Code Type Description
RXCUI
236124
Created by admin on Fri Dec 15 15:21:30 GMT 2023 , Edited by admin on Fri Dec 15 15:21:30 GMT 2023
PRIMARY RxNorm
FDA UNII
D240J05W14
Created by admin on Fri Dec 15 15:21:30 GMT 2023 , Edited by admin on Fri Dec 15 15:21:30 GMT 2023
PRIMARY
SMS_ID
100000089061
Created by admin on Fri Dec 15 15:21:30 GMT 2023 , Edited by admin on Fri Dec 15 15:21:30 GMT 2023
PRIMARY
EVMPD
SUB01561MIG
Created by admin on Fri Dec 15 15:21:30 GMT 2023 , Edited by admin on Fri Dec 15 15:21:30 GMT 2023
PRIMARY
EPA CompTox
DTXSID40952332
Created by admin on Fri Dec 15 15:21:30 GMT 2023 , Edited by admin on Fri Dec 15 15:21:30 GMT 2023
PRIMARY
MERCK INDEX
m4115
Created by admin on Fri Dec 15 15:21:30 GMT 2023 , Edited by admin on Fri Dec 15 15:21:30 GMT 2023
PRIMARY Merck Index
EVMPD
SUB62020
Created by admin on Fri Dec 15 15:21:30 GMT 2023 , Edited by admin on Fri Dec 15 15:21:30 GMT 2023
PRIMARY
PUBCHEM
16212495
Created by admin on Fri Dec 15 15:21:30 GMT 2023 , Edited by admin on Fri Dec 15 15:21:30 GMT 2023
PRIMARY
DAILYMED
D240J05W14
Created by admin on Fri Dec 15 15:21:30 GMT 2023 , Edited by admin on Fri Dec 15 15:21:30 GMT 2023
PRIMARY
ECHA (EC/EINECS)
227-809-3
Created by admin on Fri Dec 15 15:21:30 GMT 2023 , Edited by admin on Fri Dec 15 15:21:30 GMT 2023
PRIMARY
CAS
5988-51-2
Created by admin on Fri Dec 15 15:21:30 GMT 2023 , Edited by admin on Fri Dec 15 15:21:30 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY