Details
Stereochemistry | ACHIRAL |
Molecular Formula | C14H31NO |
Molecular Weight | 229.402 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCCCCCCC[N+](C)(C)[O-]
InChI
InChIKey=SYELZBGXAIXKHU-UHFFFAOYSA-N
InChI=1S/C14H31NO/c1-4-5-6-7-8-9-10-11-12-13-14-15(2,3)16/h4-14H2,1-3H3
Molecular Formula | C14H31NO |
Molecular Weight | 229.402 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Lauramine Oxide is a tertiary amine oxide. Because Lauramine Oxide has dual functional groups in the same molecule (both asidic and basic groups), it is very versatile. At a concentration of 30%, Lauramine Oxide produced severe dermal reactions in rabbits, but at 0.3% only slight to moderate erythema with slight edema. Lauramine Oxide at 0.1% in drinking water was not carcinogenic in rats. Lauramine oxide is used mainly in hair-care products such as shampoos, hair rinses, tonics and hair-grooming aids.
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Modulation of hepatitis C virus NS3 protease and helicase activities through the interaction with NS4A. | 1999 Apr 27 |
|
Resolution of the V1 ATPase from Manduca sexta into subcomplexes and visualization of an ATPase-active A3B3EG complex by electron microscopy. | 2003 Jan 3 |
|
The ionic track in the F1-ATPase from the thermophilic Bacillus PS3. | 2004 Mar 9 |
|
Purification, crystallization, and properties of F1-ATPase complexes from the thermoalkaliphilic Bacillus sp. strain TA2.A1. | 2005 Nov |
|
Overexpression and purification of the RyR1 pore-forming region. | 2007 |
|
Structural characterization of recombinant human CD81 produced in Pichia pastoris. | 2008 Feb |
|
Structure and non-essential function of glycerol kinase in Plasmodium falciparum blood stages. | 2009 Jan |
|
Reflections on my career in analytical chemistry and biochemistry. | 2010 |
|
Two different hematocrit detection methods: different methods, different results? | 2010 Mar 9 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:00:35 GMT 2023
by
admin
on
Fri Dec 15 15:00:35 GMT 2023
|
Record UNII |
4F6FC4MI8W
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Systematic Name | English | ||
|
Brand Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
C014518
Created by
admin on Fri Dec 15 15:00:35 GMT 2023 , Edited by admin on Fri Dec 15 15:00:35 GMT 2023
|
PRIMARY | |||
|
1364388
Created by
admin on Fri Dec 15 15:00:35 GMT 2023 , Edited by admin on Fri Dec 15 15:00:35 GMT 2023
|
PRIMARY | RxNorm | ||
|
216-700-6
Created by
admin on Fri Dec 15 15:00:35 GMT 2023 , Edited by admin on Fri Dec 15 15:00:35 GMT 2023
|
PRIMARY | |||
|
DB04147
Created by
admin on Fri Dec 15 15:00:35 GMT 2023 , Edited by admin on Fri Dec 15 15:00:35 GMT 2023
|
PRIMARY | |||
|
LAURYLDIMETHYLAMINE OXIDE
Created by
admin on Fri Dec 15 15:00:35 GMT 2023 , Edited by admin on Fri Dec 15 15:00:35 GMT 2023
|
PRIMARY | |||
|
15433
Created by
admin on Fri Dec 15 15:00:35 GMT 2023 , Edited by admin on Fri Dec 15 15:00:35 GMT 2023
|
PRIMARY | |||
|
SUB21624
Created by
admin on Fri Dec 15 15:00:35 GMT 2023 , Edited by admin on Fri Dec 15 15:00:35 GMT 2023
|
PRIMARY | |||
|
131762
Created by
admin on Fri Dec 15 15:00:35 GMT 2023 , Edited by admin on Fri Dec 15 15:00:35 GMT 2023
|
PRIMARY | |||
|
4F6FC4MI8W
Created by
admin on Fri Dec 15 15:00:35 GMT 2023 , Edited by admin on Fri Dec 15 15:00:35 GMT 2023
|
PRIMARY | |||
|
5451
Created by
admin on Fri Dec 15 15:00:35 GMT 2023 , Edited by admin on Fri Dec 15 15:00:35 GMT 2023
|
PRIMARY | |||
|
4F6FC4MI8W
Created by
admin on Fri Dec 15 15:00:35 GMT 2023 , Edited by admin on Fri Dec 15 15:00:35 GMT 2023
|
PRIMARY | |||
|
1643-20-5
Created by
admin on Fri Dec 15 15:00:35 GMT 2023 , Edited by admin on Fri Dec 15 15:00:35 GMT 2023
|
PRIMARY | |||
|
100000088316
Created by
admin on Fri Dec 15 15:00:35 GMT 2023 , Edited by admin on Fri Dec 15 15:00:35 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
ACTIVE MOIETY |