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Details

Stereochemistry ACHIRAL
Molecular Formula C6H15N.ClH
Molecular Weight 137.6511
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TRIETHYLAMINE HYDROCHLORIDE

SMILES

CCN(CC)CC.Cl

InChI

InChIKey=ILWRPSCZWQJDMK-UHFFFAOYSA-N
InChI=1S/C6H15N.ClH/c1-4-7(5-2)6-3;/h4-6H2,1-3H3;1H

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.4609
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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
Cell adhesion and signaling on the fibronectin 1st type III repeat; requisite roles for cell surface proteoglycans and integrins.
2001
Oriented antibody immobilization to polystyrene macrocarriers for immunoassay modified with hydrazide derivatives of poly(meth)acrylic acid.
2001
Syntheses and molecular structures of new cali.
2001
High-performance liquid chromatography assay for simultaneous determination of dextromethorphan and its main metabolites in urine and in microsomal preparations.
2001 Apr 15
Synthesis of TiRru2 heterobimetallic and TiRuM (M = Rh, Rr, Pd, Pt) heterotrimetallic sulfido clusters from a hydrosulfido-bridged titanium-ruthenium complex.
2001 Apr 23
Enantiomer separation by nonaqueous and aqueous capillary electrochromatography on cyclodextrin stationary phases.
2001 Aug
Separation of lidocaine and its metabolites by capillary electrophoresis using volatile aqueous and nonaqueous electrolyte systems.
2001 Aug
Determination of propranolol concentration in small volume of rat plasma by HPLC with fluorometric detection.
2001 Dec
Quality of odor and olfactory lateralization processes in humans.
2001 Dec
The reactions of diaminomaleonitrile with isocyanates and either aldehydes or ketones revisited.
2001 Dec 14
GnRH antagonists: a new generation of long acting analogues incorporating p-ureido-phenylalanines at positions 5 and 6.
2001 Feb 1
Validation of an HPLC method for the determination of urinary and plasma levels of N1-methylnicotinamide, an endogenous marker of renal cationic transport and plasma flow.
2001 Jan
Spectrophotometric measurement of mercaptans with 4,4'-dithiodipyridine.
2001 Jan 15
Optimised determination of clobazam in human plasma with extraction and high-performance liquid chromatography analysis.
2001 Jan 5
Efficient methods for the synthesis of [2-15N]guanosine and 2'-deoxy[2-15N]guanosine derivatives.
2001 Jan-Feb
Entomological investigations of an outbreak of Japanese encephalitis virus in the Torres Strait, Australia, in 1998.
2001 Jul
Simultaneous determination of mono-, di-, and tributyltin in sediments by isotope dilution analysis using gas chromatography--ICPMS.
2001 Jul 1
A novel mechanical dissociation technique for studying acutely isolated maturing Drosophila central neurons.
2001 Jul 30
Palladium-copper catalyzed synthesis of benzofused heterocycles with two heteroatoms: novel and highly regio- and stereoselective syntheses of (E)-2-(2-arylvinyl)-3-tosyl-2,3-dihydro-1,3-benzothiazoles and (E)-2-alkyl(aryl)idene-3,4-dihydro-2H-1,4-benzothiazines.
2001 Jun 29
Analysis of alcohols, as dimethylglycine esters, by electrospray ionization tandem mass spectrometry.
2001 Mar
Photooxygenation of the helimers of (-)-isocolchicine: regio- and facial selectivity of the [4 + 2] cycloaddition with singlet oxygen and surprising endoperoxide transformations.
2001 May 4
Development of a simplified, sensitive high-performance liquid chromatographic method using fluorescence detection to determine the concentration of UCN-01 in human plasma.
2001 Sep 5
Simultaneous determination of cloricromene and its active metabolite in rabbit aqueous humor by high-performance liquid chromatography.
2002 Feb 5
Patents
Substance Class Chemical
Created
by admin
on Sat Jun 26 11:05:06 UTC 2021
Edited
by admin
on Sat Jun 26 11:05:06 UTC 2021
Record UNII
0NX3818GCW
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TRIETHYLAMINE HYDROCHLORIDE
HSDB  
Systematic Name English
ETHANAMINE, N,N-DIETHYL-, HYDROCHLORIDE
Systematic Name English
TRIETHYLAMINE HYDROCHLORIDE [HSDB]
Common Name English
TRIETHYLAMINE MONOHYDROCHLORIDE
Systematic Name English
TRIETHYLAMINE, HYDROCHLORIDE
Systematic Name English
ETHANAMINE, N,N-DIETHYL-, HYDROCHLORIDE (1:1)
Systematic Name English
NSC-30600
Code English
N,N-DIETHYLETHANAMINE HYDROCHLORIDE
Systematic Name English
Code System Code Type Description
PUBCHEM
11130
Created by admin on Sat Jun 26 11:05:07 UTC 2021 , Edited by admin on Sat Jun 26 11:05:07 UTC 2021
PRIMARY
EPA CompTox
554-68-7
Created by admin on Sat Jun 26 11:05:07 UTC 2021 , Edited by admin on Sat Jun 26 11:05:07 UTC 2021
PRIMARY
FDA UNII
0NX3818GCW
Created by admin on Sat Jun 26 11:05:07 UTC 2021 , Edited by admin on Sat Jun 26 11:05:07 UTC 2021
PRIMARY
CAS
554-68-7
Created by admin on Sat Jun 26 11:05:07 UTC 2021 , Edited by admin on Sat Jun 26 11:05:07 UTC 2021
PRIMARY
MESH
C016162
Created by admin on Sat Jun 26 11:05:07 UTC 2021 , Edited by admin on Sat Jun 26 11:05:07 UTC 2021
PRIMARY
ECHA (EC/EINECS)
209-067-2
Created by admin on Sat Jun 26 11:05:07 UTC 2021 , Edited by admin on Sat Jun 26 11:05:07 UTC 2021
PRIMARY
HSDB
5689
Created by admin on Sat Jun 26 11:05:07 UTC 2021 , Edited by admin on Sat Jun 26 11:05:07 UTC 2021
PRIMARY
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