Details
Stereochemistry | ACHIRAL |
Molecular Formula | C4H11NO |
Molecular Weight | 89.1362 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CN(C)CCO
InChI
InChIKey=UEEJHVSXFDXPFK-UHFFFAOYSA-N
InChI=1S/C4H11NO/c1-5(2)3-4-6/h6H,3-4H2,1-2H3
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
Dose | Population | Adverse events |
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0.1 % single, topical Highest studied dose Dose: 0.1 % Route: topical Route: single Dose: 0.1 % Sources: Page: p.10 |
healthy Health Status: healthy Sources: Page: p.10 |
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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 |
PubMed
Title | Date | PubMed |
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The relationship between the interfacial properties of surfactants and their toxicity to aquatic organisms. | 2001 Mar 1 |
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Split face study on the cutaneous tensile effect of 2-dimethylaminoethanol (deanol) gel. | 2002 Aug |
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Preparation of phytate-removed deamidated soybean globulins by ion exchangers and characterization of their calcium-binding ability. | 2002 Jan 2 |
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[18F]fluoromethyl triflate, a novel and reactive [18F]fluoromethylating agent: preparation and application to the on-column preparation of [18F]fluorocholine. | 2002 Sep |
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Reactivity and molecular recognition: amine methylation by an introverted ester. | 2003 Dec 3 |
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Efficacy of dimethylaminoethanol (DMAE) containing vitamin-mineral drug combination on EEG patterns in the presence of different emotional states. | 2003 May 30 |
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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 |
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[Fluorescent-labeled lipophilic analogues of serotonin, dopamine, and acetylcholine: synthesis, mass spectrometry, and biological activity]. | 2004 Sep-Oct |
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The role of dimethylaminoethanol in cosmetic dermatology. | 2005 |
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C-terminal sequencing method for proteins in polyacrylamide gel by the reaction of acetic anhydride. | 2006 Apr |
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The evolution of senescence and post-reproductive lifespan in guppies (Poecilia reticulata). | 2006 Jan |
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A new design strategy for dispersion stabilization of Ni particles based on the surface acid and base properties of Ni particles. | 2007 Aug 15 |
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Synthesis and characterization of succinylcholine-d18 and succinylmonocholine-d3 designed for simultaneous use as internal standards in mass spectrometric analyses. | 2007 Jul |
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Improved automated synthesis of [18F]fluoroethylcholine as a radiotracer for cancer imaging. | 2007 May 1 |
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Mannosylated poly(ethylene oxide)-b-poly(epsilon-caprolactone) diblock copolymers: synthesis, characterization, and interaction with a bacterial lectin. | 2007 Sep |
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Synthesis, cytotoxicity, DNA interaction, and topoisomerase II inhibition properties of novel indeno[2,1-c]quinolin-7-one and indeno[1,2-c]isoquinolin-5,11-dione derivatives. | 2008 Jun 26 |
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Quantitative determination of dimethylaminoethanol in cosmetic formulations by nuclear magnetic resonance spectroscopy. | 2008 Nov-Dec |
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Mesotherapy - The french connection. | 2010 Jan |
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The choC gene encoding a putative phospholipid methyltransferase is essential for growth and development in Aspergillus nidulans. | 2010 Jun |
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C265
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DSLD |
1303 (Number of products:461)
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WHO-VATC |
QN06BX04
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WHO-ATC |
N06BX04
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2652
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100000091061
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1329
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2N6K9DRA24
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D003642
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7902
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SUB13534MIG
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3116
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108-01-0
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787
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DTXSID2020505
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SUB13536MIG
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ALTERNATIVE | |||
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DIMETHYLETHANOLAMINE
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271436
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DB13352
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C72733
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2N6K9DRA24
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m4115
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203-542-8
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DEANOL
Created by
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PRIMARY | Dimethylethanolamine is used in the preparation of water-reducible coating formulations. Government regulations covering the amount of organic solvent allowable in the air have spurred a search for emission control procedures. One of the most promising is the replacement of the organic solvent by water. The resins used in coating formulations are not water soluble, but can be made so by reacting them with the amine. |
ACTIVE MOIETY
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