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

Details

Stereochemistry ACHIRAL
Molecular Formula C2H7N.BrH
Molecular Weight 125.996
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETHYLAMINE HYDROBROMIDE

SMILES

Br.CCN

InChI

InChIKey=PNZDZRMOBIIQTC-UHFFFAOYSA-N
InChI=1S/C2H7N.BrH/c1-2-3;/h2-3H2,1H3;1H

HIDE SMILES / InChI

Molecular Formula BrH
Molecular Weight 80.912
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C2H7N
Molecular Weight 45.0837
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
[Degradation of methamidophos by Saccharomyces rouxii WY-3].
2001 Jul
Phenolic modification as an approach to improve the pharmacology of the 3-acyloxy-2-benzylpropyl homovanillic amides and thioureas, a promising class of vanilloid receptor agonists and analgesics.
2002 Apr
[Study on adductive reaction of Ni[(C4H9O)2PS2]2 with nitrogen base by spectrophotometric method(II)].
2002 Aug
Modified high amylose starch for immobilization of uricase for therapeutic application.
2002 Dec
Further evidence for suicide inhibition of semicarbazide-sensitive amine oxidase in guinea pig lung by 2-bromoethylamine.
2003 Dec
Identification of clinically relevant Trichosporon species.
2003 Feb
Titanium(IV) tungstosilicate and titanium(IV) tungstophosphate: two new inorganic ion exchangers.
2003 Feb 14
Rapid fluorimetric assay for primary amine groups in water samples.
2003 Jul
Pyrrolidinobenzoic acid inhibitors of influenza virus neuraminidase: modifications of essential pyrrolidinone ring substituents.
2003 Jul 3
Synthesis and pharmacological characterization of a series of geometrically constrained 5-HT(2A/2C) receptor ligands.
2003 Jul 31
Characterization of labelling and de-labelling reagents for detection and recovery of tyrosine residue in peptide.
2003 Mar-Apr
Polyvinylalcohol three-dimensional matrices for improved long-term dynamic culture of hepatocytes.
2003 Sep 1
[Hygienic standards of the occupational air quality established by the Experts on Chemical Agents, 2002].
2004
Gas phase reactivity of isomeric arylglycosides towards amines. A chemical ionization mass spectrometry and tandem mass spectrometry study.
2004 Feb
Cyclic amidine sugars as transition-state analogue inhibitors of glycosidases: potent competitive inhibitors of mannosidases.
2004 Feb 25
Simple synthesis of a weak nucleophilic base (4-ethyl-2,6-diisopropyl-3,5-dimethylpyridine) evidencing a double Janus group effect.
2004 Jan 23
Visualization of PLP-bound intermediates in hemeless variants of human cystathionine beta-synthase: evidence that lysine 119 is a general base.
2004 Jul 15
Separation and conductimetric detection of C1-C7 aliphatic monocarboxylic acids and C1-C7 aliphatic monoamines on unfunctionized polymethacrylate resin columns.
2004 Jun 11
Conservation of mechanism in three chorismate-utilizing enzymes.
2004 Mar 3
Systematics of the anamorphic basidiomycetous yeast genus Trichosporon Behrend with the description of five novel species: Trichosporon vadense, T. smithiae, T. dehoogii, T. scarabaeorum and T. gamsii.
2004 May
Isolation of genomic DNA using magnetic cobalt ferrite and silica particles.
2004 Nov 12
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 06:50:18 GMT 2023
Edited
by admin
on Sat Dec 16 06:50:18 GMT 2023
Record UNII
10430J81ZZ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ETHYLAMINE HYDROBROMIDE
Systematic Name English
ETHYLAMINE MONOHYDROBROMIDE
Systematic Name English
NSC-4117
Code English
ETHYLAMMONIUM BROMIDE
Systematic Name English
ETHANAMINE, HYDROBROMIDE
Systematic Name English
ETHANAMINE, HYDROBROMIDE (1:1)
Systematic Name English
ETHYLAMINE, HYDROBROMIDE
Systematic Name English
Classification Tree Code System Code
DEA NO. 8678
Created by admin on Sat Dec 16 06:50:18 GMT 2023 , Edited by admin on Sat Dec 16 06:50:18 GMT 2023
Code System Code Type Description
ECHA (EC/EINECS)
209-797-1
Created by admin on Sat Dec 16 06:50:18 GMT 2023 , Edited by admin on Sat Dec 16 06:50:18 GMT 2023
PRIMARY
MESH
C041564
Created by admin on Sat Dec 16 06:50:18 GMT 2023 , Edited by admin on Sat Dec 16 06:50:18 GMT 2023
PRIMARY
FDA UNII
10430J81ZZ
Created by admin on Sat Dec 16 06:50:18 GMT 2023 , Edited by admin on Sat Dec 16 06:50:18 GMT 2023
PRIMARY
NSC
4117
Created by admin on Sat Dec 16 06:50:18 GMT 2023 , Edited by admin on Sat Dec 16 06:50:18 GMT 2023
PRIMARY
EPA CompTox
DTXSID1060475
Created by admin on Sat Dec 16 06:50:18 GMT 2023 , Edited by admin on Sat Dec 16 06:50:18 GMT 2023
PRIMARY
CAS
593-55-5
Created by admin on Sat Dec 16 06:50:18 GMT 2023 , Edited by admin on Sat Dec 16 06:50:18 GMT 2023
PRIMARY
PUBCHEM
68974
Created by admin on Sat Dec 16 06:50:18 GMT 2023 , Edited by admin on Sat Dec 16 06:50:18 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE