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Details

Stereochemistry ACHIRAL
Molecular Formula C4H11N.ClH
Molecular Weight 109.598
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TERT-BUTYLAMINE HYDROCHLORIDE

SMILES

Cl.CC(C)(C)N

InChI

InChIKey=DLDIDQIZPBIVNQ-UHFFFAOYSA-N
InChI=1S/C4H11N.ClH/c1-4(2,3)5;/h5H2,1-3H3;1H

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C4H11N
Molecular Weight 73.1368
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Erbumine (tert-butylamine) is a colorless liquid with an ammonia-like odor. It is used in the preparation of insecticides, pharmaceuticals, oil additives, and rubber accelerators. It neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated in combination with strong reducing agents, such as hydrides.

Approval Year

PubMed

PubMed

TitleDatePubMed
Novel small molecule glucagon-like peptide-1 receptor agonist stimulates insulin secretion in rodents and from human islets.
2010-12
(tert-Butyl-imido)bis-(η-cyclo-penta-dien-yl)pyridine-zirconium(IV).
2010-08-28
Towards molecular diversity: dealkylation of tert-butyl amine in Ugi-type multicomponent reaction product establishes tert-butyl isocyanide as a useful convertible isonitrile.
2010-08-21
2-Methyl-propan-2-aminium 4-hy-droxy-benzoate.
2010-06-18
"Turn-on" fluorescent polymeric microparticle sensors for the determination of ammonia and amines in the vapor state.
2010-06
Preparation of N-acetyl, tert-butyl amide derivatives of the 20 natural amino acids.
2010-03
Step-mediated anisotropic adsorption and condensation of tert-butylamine on Cu(111).
2010-02-01
Effect of guest-host hydrogen bonding on the structures and properties of clathrate hydrates.
2010-01-18
Novel synthesis of ureas: application of t-butylureas.
2010-01
Applications of chitin and its derivatives in biological medicine.
2010
Structural transformations of sVI tert-butylamine hydrates to sII binary hydrates with methane.
2009-10-22
Synthesis, crystal structure and spectroscopic properties of a novel carbacylamidophosphate: N-(3-nitrobenzoyl)-N',N''-bis(tert-butyl)phosphoric triamide.
2009-08
Stabilization of quinapril by incorporating hydrogen bonding interactions.
2009-07
Titanium hydroamination catalysts bearing a 2-aminopyrrolinato spectator ligand: monitoring the individual reaction steps.
2009-06-21
Hydrogen storage in double clathrates with tert-butylamine.
2009-06-18
tert-Butyl-aminium phosphite.
2009-02-28
An acyclic dimer of cyclodiphosphazane {(t)BuHN((t)BuNP)2OCH2}2 containing alkoxo and amido functionalities: synthesis, derivatization, Bi- (Pd(II), Rh(I)), and tetranuclear (Pd(II), Au(I), Rh(I)Au(I)) transition metal complexes.
2009-02-16
One ring to bind them all: shape-selective complexation of phenylenediamine isomers with cucurbit[6]uril in the gas phase.
2009-02-12
N,N-Bis(2-pyridylmeth-yl)-tert-butyl-amine.
2009-01-28
Catalytic mechanism of nitrile hydratase proposed by time-resolved X-ray crystallography using a novel substrate, tert-butylisonitrile.
2008-12-26
tert-Butyl-ammonium 2,3,4,5-tetra-chloro-6-methoxy-carbonyl-benzoate.
2008-11-13
Role of key transmembrane residues in agonist and antagonist actions at the two conformations of the human beta1-adrenoceptor.
2008-11
Formation of an exciplex with mixed ligands in the mercury-photosensitized luminescence of alcohol-amine mixtures in the liquid phase.
2008-07
The use of microcalorimetry and HPLC for the determination of degradation kinetics and thermodynamic parameters of Perindopril Erbumine in aqueous solutions.
2008-05-22
Isolation and characterization of a neutral imino-semiquinone radical.
2008-05-07
The Rap-RapGAP complex: GTP hydrolysis without catalytic glutamine and arginine residues.
2008-04-09
Evaluation of impurities level of perindopril tert-butylamine in tablets.
2007-09-03
Synthesis and evaluation of L-glutamic Acid analogs as potential anticancer agents.
2007-03-28
The formation of endo-complexes between calixarenes and amines--a reinvestigation.
2006-07
Dynamics of an [Fe4S4(SPh)4]2- cluster explored via IR, Raman, and nuclear resonance vibrational spectroscopy (NRVS)-analysis using 36S substitution, DFT calculations, and empirical force fields.
2006-05-14
Investigation of the electrochemical oxidation products of zotepine and their fragmentation using on-line electrochemistry/electrospray ionization mass spectrometry.
2006-05
Dizinc alkoxides and amides supported by binucleating bis(amidoamine) ligands.
2006-02-20
Structural transition and tuning of tert-butylamine hydrate.
2005-12-02
99mTcN complexes of tert-butyl dithiocarbamate and methoxyisobutyl dithiocarbamate as myocardial and brain imaging agents.
2005-11
Human erythrocyte delta-aminolevulinate dehydratase inhibition by monosaccharides is not mediated by oxidation of enzyme sulfhydryl groups.
2005-08
Distribution of amines in water/AOT/n-hexane reverse micelles: influence of the amine chemical structure.
2005-06-01
Enantioselective nitrile anion cyclization to substituted pyrrolidines. A highly efficient synthesis of (3S,4R)-N-tert-butyl-4-arylpyrrolidine-3-carboxylic acid.
2005-04-29
Thiol-reactive clenbuterol analogues conjugated to bovine serum albumin.
2005-01-26
Kinetic stability of heteroleptic (beta-diketiminato) heavier alkaline-earth (Ca, Sr, Ba) amides.
2005-01-21
An unusual zwitterionic, diradical intermediate in photochemical electron-transfer substitution reactions.
2004-10-13
ATR-FTIR characterization of transport properties of benzoic acid ion-pairs in silicone membranes.
2004-09-28
A general study of [(eta5-Cp')2Ti(eta2-Me3SiC2SiMe3)]-catalyzed hydroamination of terminal alkynes: regioselective formation of Markovnikov and anti-Markovnikov products and mechanistic explanation (Cp'=C5H5, C5H4Et, C5Me5).
2004-05-17
Competing sulfonylation and phosphonylation following rearrangement of an O-sulfonyl-N-phosphinoylhydroxylamine with tert-butylamine: demonstration of a phosphonamidic-sulfonic anhydride intermediate and 18O-labelling evidence on how it may be formed.
2003-10-07
Application of an alkyl-diol silica precolumn in a column-switching system for the determination of meloxicam in plasma.
2003-08-08
Cucurbit[6]uril pseudorotaxanes: distinctive gas-phase dissociation and reactivity.
2003-08-06
Increasing rates and scope of reactions: sluggish amines in microwave-heated aminocarbonylation reactions under air.
2003-07-11
Transannular reactions of two parallel 1,3-butadiynes: syntheses, structures, and reactions of 1-azacyclotetradeca-3,5,10,12-tetrayne derivatives.
2003-04-14
Diminished reactivity of ortho-substituted phenacyl bromides toward nucleophilic displacement.
2003-02-21
Optical sensor for amine vapors based on dimer-monomer equilibrium of indium(III) octaethylporphyrin in a polymeric film.
2003-01-15
A piezoelectric quartz crystal sensor array self assembled calixarene bilayers for detection of volatile organic amine in gas.
2002-07-19
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:35:01 GMT 2025
Edited
by admin
on Mon Mar 31 19:35:01 GMT 2025
Record UNII
7B1QGR5JY2
Record Status Validated (UNII)
Record Version
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Name Type Language
TERT-BUTYLAMINE HYDROCHLORIDE
MI  
Systematic Name English
NSC-227859
Preferred Name English
2-PROPANAMINE, 2-METHYL-, HYDROCHLORIDE
Systematic Name English
1,1-DIMETHYLETHYLAMINE HYDROCHLORIDE
Systematic Name English
BUTYLAMINE HYDROCHLORIDE, TERT-
Systematic Name English
TERT-BUTYLAMINE HYDROCHLORIDE [MI]
Common Name English
TERT-BUTYLAMINE, HYDROCHLORIDE
Systematic Name English
2-PROPANAMINE, 2-METHYL-, HYDROCHLORIDE (1:1)
Systematic Name English
T-BUTYLAMINE HYDROCHLORIDE
Systematic Name English
Code System Code Type Description
FDA UNII
7B1QGR5JY2
Created by admin on Mon Mar 31 19:35:01 GMT 2025 , Edited by admin on Mon Mar 31 19:35:01 GMT 2025
PRIMARY
CAS
10017-37-5
Created by admin on Mon Mar 31 19:35:01 GMT 2025 , Edited by admin on Mon Mar 31 19:35:01 GMT 2025
PRIMARY
MERCK INDEX
m2817
Created by admin on Mon Mar 31 19:35:01 GMT 2025 , Edited by admin on Mon Mar 31 19:35:01 GMT 2025
PRIMARY Merck Index
NSC
227859
Created by admin on Mon Mar 31 19:35:01 GMT 2025 , Edited by admin on Mon Mar 31 19:35:01 GMT 2025
PRIMARY
EPA CompTox
DTXSID4064894
Created by admin on Mon Mar 31 19:35:01 GMT 2025 , Edited by admin on Mon Mar 31 19:35:01 GMT 2025
PRIMARY
MESH
C025397
Created by admin on Mon Mar 31 19:35:01 GMT 2025 , Edited by admin on Mon Mar 31 19:35:01 GMT 2025
PRIMARY
ECHA (EC/EINECS)
233-009-5
Created by admin on Mon Mar 31 19:35:01 GMT 2025 , Edited by admin on Mon Mar 31 19:35:01 GMT 2025
PRIMARY
PUBCHEM
82292
Created by admin on Mon Mar 31 19:35:01 GMT 2025 , Edited by admin on Mon Mar 31 19:35:01 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE