Page last updated: 2024-11-05

isobutylamine

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

Isobutylamine, also known as 2-methylpropan-1-amine, is a primary amine with the chemical formula (CH3)2CHCH2NH2. It is a colorless liquid with an ammonia-like odor. Isobutylamine is a common reagent in organic chemistry, used in the synthesis of various compounds, including pharmaceuticals, agrochemicals, and polymers. It is also used as a solvent and a catalyst in various industrial processes. Isobutylamine is synthesized from isobutyl alcohol via amination reaction with ammonia. The reaction typically involves a catalyst such as a metal oxide or a zeolite. Isobutylamine is a versatile intermediate in organic synthesis and has several biological activities, including antibacterial, antifungal, and antitumor properties. It is also used as a corrosion inhibitor and a stabilizer in various applications. The study of isobutylamine focuses on its potential applications in various fields, including medicine, agriculture, and industry. Researchers are investigating its biological activities, its synthesis methods, and its environmental impact.'

2-methylpropanamine : An alkylamine having isobutyl as the alkyl group. It has been isolated from Sambucus nigra (Elderberry). [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

FloraRankFlora DefinitionFamilyFamily Definition
SambucusgenusA plant genus in the family CAPRIFOLIACEAE known for elderberries.[MeSH]Viburnaceae[no description available]
Sambucus nigraspeciesA plant species in the genus SAMBUCUS, known for the elderberry fruit. The plant is also a source of Sambucus nigra lectins and ribosome-inactivating protein.[MeSH]Viburnaceae[no description available]

Cross-References

ID SourceID
PubMed CID6558
CHEBI ID15997
MeSH IDM0151600

Synonyms (65)

Synonym
3-methyl-2-propylamine
1-propanamine, 2-methyl-
1-amino-2-methylpropane
valamine
nsc-8028
wln: z1y1&1
2-methylpropylamine
monoisobutylamine
nsc8028
iso-butylamine
2-methyl-1-aminopropane
CHEBI:15997
i-butylamine
iso-c4h9nh2
inchi=1/c4h11n/c1-4(2)3-5/h4h,3,5h2,1-2h
ccris 6250
hsdb 612
einecs 201-145-4
un1214
nsc 8028
ai3-24039
isobutylamine
78-81-9
2-methylpropanamine
2-methylpropan-1-amine
C02787
2-methyl-1-propanamine
isobutylamine, 99%
FT-0695051
I0095
AKOS000119607
unii-1h60h4lohz
1h60h4lohz ,
isobutylamine [un1214] [flammable liquid]
FT-0607317
2-methylpropyl amine
isobutyl amine
i-bunh2
2-methylpropane-1-amine
isobutyl-amine
n-iso-butylamine
ibunh2
(2-methylpropyl)amine
iso-butyl amine
isobutylamine [hsdb]
isobutylamine [mi]
amino-2-methyl propane, 1-
isobutylamine [fhfi]
fema no. 4239
un 1214
mfcd00008146
DTXSID9025459
2-methyl-1-propylamine
J-510080
F2190-0360
isobutylamine, purum, >=98.0% (gc)
isobutylamine, analytical standard
valamine?
isobutylamine, 8ci
2-methyl-1-propanamine, 9ci
Q416655
1-amino-2-methyl-propane
STL183318
STR01259
EN300-20218
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
plant metaboliteAny eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (1)

ClassDescription
alkylaminesAny amine formally derived from ammonia by replacing one, two or three hydrogen atoms by alkyl groups.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Research

Studies (10)

TimeframeStudies, This Drug (%)All Drugs %
pre-19902 (20.00)18.7374
1990's2 (20.00)18.2507
2000's5 (50.00)29.6817
2010's1 (10.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 51.64

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be very strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index51.64 (24.57)
Research Supply Index2.48 (2.92)
Research Growth Index4.56 (4.65)
Search Engine Demand Index76.22 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (51.64)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other11 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]