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About This Item
Linear Formula:
(CH3)2CHCH2NH2
CAS Number:
Molecular Weight:
73.14
UNSPSC Code:
85151701
NACRES:
NA.24
PubChem Substance ID:
EC Number:
201-145-4
Beilstein/REAXYS Number:
385626
MDL number:
grade
analytical standard
Quality Level
assay
≥99.0% (GC)
shelf life
limited shelf life, expiry date on the label
impurities
≤1.0% water
refractive index
n20/D 1.397 (lit.), n20/D 1.396-1.398
bp
64-71 °C (lit.)
mp
−85 °C (lit.)
density
0.736 g/mL at 25 °C (lit.)
application(s)
cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care
format
neat
SMILES string
CC(C)CN
InChI
1S/C4H11N/c1-4(2)3-5/h4H,3,5H2,1-2H3
InChI key
KDSNLYIMUZNERS-UHFFFAOYSA-N
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Flam. Liq. 2 - Skin Corr. 1A
Storage Class
3 - Flammable liquids
wgk
WGK 1
flash_point_f
15.8 °F - closed cup
flash_point_c
-9 °C - closed cup
Regulatory Information
危险化学品
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Mirlinda Biba et al.
Journal of chromatography. A, 1363, 250-256 (2014-08-02)
Fast chiral supercritical fluid chromatography (SFC) separations have become important due to the increasing use of high-throughput experimentation (HTE) in organic synthesis. These HTE experiments can generate hundreds of samples for chiral analysis that need to be assayed in a
Lars Erik Uggerhøj et al.
FEBS letters, 588(17), 3291-3297 (2014-07-27)
The inclusion of peptoid monomers into antimicrobial peptides (AMPs) increases their proteolytic resistance, but introduces conformational flexibility (reduced hydrogen bonding ability and cis/trans isomerism). We here use NMR spectroscopy to answer how the insertion of a peptoid monomer influences the


