U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C6H15N
Molecular Weight 101.1902
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TRIETHYLAMINE

SMILES

CCN(CC)CC

InChI

InChIKey=ZMANZCXQSJIPKH-UHFFFAOYSA-N
InChI=1S/C6H15N/c1-4-7(5-2)6-3/h4-6H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C6H15N
Molecular Weight 101.1902
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
1.17 μM
25 mg single, oral
dose: 25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
TRIETHYLAMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
3.81 μM × h
137 μmol single, intravenous
dose: 137 μmol
route of administration: Intravenous
experiment type: SINGLE
co-administered:
TRIETHYLAMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
5.46 μM × h
25 mg single, oral
dose: 25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
TRIETHYLAMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
3.7 h
137 μmol single, intravenous
dose: 137 μmol
route of administration: Intravenous
experiment type: SINGLE
co-administered:
TRIETHYLAMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
2.9 h
25 mg single, oral
dose: 25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
TRIETHYLAMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
PubMed

PubMed

TitleDatePubMed
Preliminary study of the analysis of oligogalacturonic acids by electrospray ionization mass spectrometry.
2001
Syntheses and molecular structures of new cali.
2001
Simultaneous analysis of clozapine, clomipramine and their metabolites by reversed-phase liquid chromatography.
2001 Apr
The rapid quantitative analysis of phenprobamate and acetaminophen by RP-LC and compensation technique.
2001 Apr
Validated high-performance liquid chromatographic assay for simultaneous determination of dacarbazine and the plasma metabolites 5-(3-hydroxymethyl-3-methyl-1-triazeno)imidazole-4-carboxamide and 5-(3-methyl-1-triazeno)imidazole-4-carboxamide.
2001 Apr 15
High-performance liquid chromatography assay for simultaneous determination of dextromethorphan and its main metabolites in urine and in microsomal preparations.
2001 Apr 15
An improved (32)P-postlabeling assay for the sensitive detection of 8-oxodeoxyguanosine in tissue DNA.
2001 Aug
Ionic blockade of the rat connexin40 gap junction channel by large tetraalkylammonium ions.
2001 Dec
Determination of haloacetic acids in aqueous environments by solid-phase extraction followed by ion-pair liquid chromatography-electrospray ionization mass spectrometric detection.
2001 Dec 14
Clean-up procedures for the analysis of heterocyclic aromatic amines (aminoazaarenes) from heat-treated meat samples.
2001 Dec 14
Systematic structural coordination chemistry of p-tert-butyltetrathiacalix[4]arene: 1. Group 1 elements and congeners.
2001 Feb 12
Spectroscopic study on the photoinduced reaction of fullerene C60 with aliphatic amines and its dynamics--strong short wavelength fluorescence from the adducts.
2001 Jan
Photoreductive dehalogenation of halogenated benzene derivatives using ZnS or CdS nanocrystallites as photocatalysts.
2001 Jan 1
Palladium-catalyzed heteroannulation leading to heterocyclic structures with two heteroatoms: a highly regio- and stereoselective synthesis of (Z)-4-alkyl-2-alkyl(aryl)idene-3,4-dihydro-2H-1,4-benzoxazines and (Z)-3-alkyl(aryl)idene-4-tosyl-3,4-dihydro-2H-1,4-benzoxazines.
2001 Jan 12
Capillary electrophoresis of high-molecular chitosan: the natural carbohydrate biopolymer.
2001 Jul
Substrate-dependent chemoselective aldose-aldose and aldose-ketose isomerizations of carbohydrates promoted by a combination of calcium ion and monoamines.
2001 Jul 19
Direct separation of captopril diastereoisomers including their rotational isomers by RP-LC using a teicoplanin column.
2001 Jun
Can conditioned histamine release occur under urethane anesthesia in guinea pigs?
2001 Mar
Specific and non-specific measurements of tissue angiotensin II cascade members.
2001 Mar
Development of liquid chromatographic method for the analysis of kanamycin residues in varicella vaccine using phenylisocyanate as a derivatization reagent.
2001 Mar 5
High-performance liquid chromatographic analysis of a new neuroprotective agent for ischemia-reperfusion damage, KR-31378.
2001 Mar-Apr
Switch-over in photochemical reaction mechanism from hydrogen abstraction to exciplex-induced quenching: interaction of triplet-excited versus singlet-excited acetone versus cumyloxyl radicals with amines.
2001 Oct 10
Palladium-catalyzed tandem dimerization and cyclization of acetylenic ketones: a convenient method for 3,3'-bifurans using PdCl2(PPh3)2.
2001 Sep 7
Simultaneous determination of cloricromene and its active metabolite in rabbit aqueous humor by high-performance liquid chromatography.
2002 Feb 5
Excited state proton transfer reaction of two new intramolecularly hydrogen bonded Schiff bases at room temperature and 77K.
2002 Jan 1
Patents
Substance Class Chemical
Created
by admin
on Fri Jun 25 22:43:22 UTC 2021
Edited
by admin
on Fri Jun 25 22:43:22 UTC 2021
Record UNII
VOU728O6AY
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TRIETHYLAMINE
FHFI   HSDB   MI   USP-RS  
Systematic Name English
FEMA NO. 4246
Code English
ETHANAMINE, N,N-DIETHYL-
Systematic Name English
TRIETHYLAMINE [MI]
Common Name English
TRIETHYLAMINE [FHFI]
Common Name English
N,N-DIETHYLETHANAMINE
Systematic Name English
TRIETHYLAMINE [USP-RS]
Common Name English
(DIETHYLAMINO)ETHANE
Systematic Name English
TRIETHYLAMINE [INCI]
Common Name English
TRIETHYLAMINE [HSDB]
Common Name English
Classification Tree Code System Code
JECFA EVALUATION TRIETHYLAMINE
Created by admin on Fri Jun 25 22:43:22 UTC 2021 , Edited by admin on Fri Jun 25 22:43:22 UTC 2021
Code System Code Type Description
ECHA (EC/EINECS)
204-469-4
Created by admin on Fri Jun 25 22:43:22 UTC 2021 , Edited by admin on Fri Jun 25 22:43:22 UTC 2021
PRIMARY
HSDB
896
Created by admin on Fri Jun 25 22:43:22 UTC 2021 , Edited by admin on Fri Jun 25 22:43:22 UTC 2021
PRIMARY
RXCUI
1307097
Created by admin on Fri Jun 25 22:43:22 UTC 2021 , Edited by admin on Fri Jun 25 22:43:22 UTC 2021
PRIMARY RxNorm
PUBCHEM
8471
Created by admin on Fri Jun 25 22:43:22 UTC 2021 , Edited by admin on Fri Jun 25 22:43:22 UTC 2021
PRIMARY
MESH
C016162
Created by admin on Fri Jun 25 22:43:22 UTC 2021 , Edited by admin on Fri Jun 25 22:43:22 UTC 2021
PRIMARY
WIKIPEDIA
TRIETHYLAMINE
Created by admin on Fri Jun 25 22:43:22 UTC 2021 , Edited by admin on Fri Jun 25 22:43:22 UTC 2021
PRIMARY
CAS
121-44-8
Created by admin on Fri Jun 25 22:43:22 UTC 2021 , Edited by admin on Fri Jun 25 22:43:22 UTC 2021
PRIMARY
FDA UNII
VOU728O6AY
Created by admin on Fri Jun 25 22:43:22 UTC 2021 , Edited by admin on Fri Jun 25 22:43:22 UTC 2021
PRIMARY
EVMPD
SUB130556
Created by admin on Fri Jun 25 22:43:22 UTC 2021 , Edited by admin on Fri Jun 25 22:43:22 UTC 2021
PRIMARY
EPA CompTox
121-44-8
Created by admin on Fri Jun 25 22:43:22 UTC 2021 , Edited by admin on Fri Jun 25 22:43:22 UTC 2021
PRIMARY
USP_CATALOG
1683559
Created by admin on Fri Jun 25 22:43:22 UTC 2021 , Edited by admin on Fri Jun 25 22:43:22 UTC 2021
PRIMARY USP-RS
MERCK INDEX
M11101
Created by admin on Fri Jun 25 22:43:22 UTC 2021 , Edited by admin on Fri Jun 25 22:43:22 UTC 2021
PRIMARY Merck Index
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT