Skip to Content
Merck
CN

06755

Isobutylamine

analytical standard

Synonym(s):

1-Amino-2-methylpropane

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

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:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


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



Still not finding the right product?

Explore all of our products under Isobutylamine


signalword

Danger

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

This item has



Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library



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