ERBUMINE

Details

Stereochemistry	ACHIRAL
Molecular Formula	C4H11N
Molecular Weight	73.1368
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

CC(C)(C)N

InChI

InChIKey=YBRBMKDOPFTVDT-UHFFFAOYSA-N

InChI=1S/C4H11N/c1-4(2,3)5/h5H2,1-3H3

HIDE SMILES / InChI

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

Description
Sources: https://nj.gov/health/eoh/rtkweb/documents/fs/3025.pdf | https://cameochemicals.noaa.gov/chemical/8358

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

Title	Date	PubMed
A piezoelectric quartz crystal sensor array self assembled calixarene bilayers for detection of volatile organic amine in gas.	2002 Jul 19	18968724
The new generation dihydropyridine type calcium blockers, bearing 4-phenyl oxypropanolamine, display alpha-/beta-adrenoceptor antagonist and long-acting antihypertensive activities.	2002 Mar	11814861
Intramolecular and intermolecular N-H...C(5)H(5)(-) hydrogen bonding in magnesocene adducts of alkylamines. Implications for chemical vapor deposition using cyclopentadienyl source compounds.	2002 Sep 25	12236729
Cucurbit[6]uril pseudorotaxanes: distinctive gas-phase dissociation and reactivity.	2003 Aug 6	12889944
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 Oct 7	14584802
An unusual zwitterionic, diradical intermediate in photochemical electron-transfer substitution reactions.	2004 Oct 13	15469246
Dizinc alkoxides and amides supported by binucleating bis(amidoamine) ligands.	2006 Feb 20	16471998
Formation of an exciplex with mixed ligands in the mercury-photosensitized luminescence of alcohol-amine mixtures in the liquid phase.	2008 Jul	17804285
tert-Butyl-ammonium 2,3,4,5-tetra-chloro-6-methoxy-carbonyl-benzoate.	2008 Nov 13	21581294
tert-Butyl-aminium phosphite.	2009 Feb 28	21582288
N,N-Bis(2-pyridylmeth-yl)-tert-butyl-amine.	2009 Jan 28	21581995
Stabilization of quinapril by incorporating hydrogen bonding interactions.	2009 Jul	20502545
Applications of chitin and its derivatives in biological medicine.	2010	21614199
Towards molecular diversity: dealkylation of tert-butyl amine in Ugi-type multicomponent reaction product establishes tert-butyl isocyanide as a useful convertible isonitrile.	2010 Aug 21	20574586
Novel small molecule glucagon-like peptide-1 receptor agonist stimulates insulin secretion in rodents and from human islets.	2010 Dec	20823098

Patents

Substance Class	Chemical Created by `admin` on `Fri Dec 15 18:38:57 GMT 2023` Edited by `admin` on `Fri Dec 15 18:38:57 GMT 2023`
Record UNII	91Z53KF68U
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

ERBUMINE

Official Name

English

2-METHYLPROPAN-2-AMINE

Systematic Name

English

1,1-DIMETHYLETHYLAMINE

Systematic Name

English

NSC-9571

Code

English

T-BUTYLAMINE

Common Name

English

TERT-BUTYLAMINE

Systematic Name

English

TERT-BUTYLAMINE [MI]

Common Name

English

2-PROPANAMINE, 2-METHYL-

Common Name

English

BUTYLAMINE, TERT-

Systematic Name

English

erbumine [INN]

Common Name

English

2-METHYL-2-PROPANAMINE [HSDB]

Common Name

English

Code System Code Type Description

NSC

9571