Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

59330

Sigma-Aldrich

Isopropylamine

≥97.0% (GC)

Synonym(s):

2-Aminopropane

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
(CH3)2CHNH2
CAS Number:
75-31-0
Molecular Weight:
59.11
Beilstein:
605259
EC Number:
200-860-9
MDL number:
MFCD00008082
UNSPSC Code:
12352100
PubChem Substance ID:
57651680
NACRES:
NA.22

vapor density

2.04 (vs air)

vapor pressure

9.2 psi ( 20 °C)

Assay

≥97.0% (GC)

form

liquid

autoignition temp.

755 °F

expl. lim.

10.4 %

impurities

≤3% water

refractive index

n20/D 1.374 (lit.)
n20/D 1.374

bp

32-35 °C
33-34 °C (lit.)

density

0.688 g/mL at 20 °C (lit.)

functional group

amine

storage temp.

2-8°C

SMILES string

CC(C)N

InChI

1S/C3H9N/c1-3(2)4/h3H,4H2,1-2H3

InChI key

JJWLVOIRVHMVIS-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 1 - Skin Corr. 1A - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

<-13.0 °F - closed cup

Flash Point(C)

<= -25 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCM3754
BCCH8953
BCCL4108
BCCK9146
BCCC6592

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.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Donna L McGovern et al.
Journal of molecular graphics & modelling, 28(7), 612-625 (2010-01-20)
The highly potent and kappa-opioid (KOP) receptor-selective hallucinogen Salvinorin A and selected analogs have been analyzed using the 3D quantitative structure-affinity relationship technique Comparative Molecular Field Analysis (CoMFA) in an effort to derive a statistically significant and predictive model of
M Ashraf-Khorassani et al.
Journal of chromatography. A, 1229, 237-248 (2012-02-07)
A thorough evaluation of 5 μm bare silica from two major vendors for achiral supercritical fluid chromatography of polar analytes has been carried out. Columns were the same dimension, and a virgin column was reserved for each modifier-mixture combination. Three
Chaw Jiang Lim et al.
Pest management science, 69(1), 104-111 (2012-08-07)
Pesticides are developed with carriers to improve their physicochemical properties and, accordingly, the bioefficacy of the applied formulation. For foliar-applied herbicide, generally less than 0.1% of the active ingredient reaching the target site could reduce pesticide performance. Recently, a carrier
Gabriel Vallejos et al.
Bioorganic & medicinal chemistry, 13(14), 4450-4457 (2005-05-24)
The in vitro monoamine oxidase inhibitory (MAOI) activities of 11 heteroarylisopropylamines vis-à-vis MAO-A and MAO-B were described and interpreted in terms of possible interactions with the enzyme active site. Molecular dynamics simulations allowed a comparison between the most active MAO-A
Jacek Lipok et al.
Ecotoxicology and environmental safety, 73(7), 1681-1688 (2010-09-04)
The toxicity of commercial formulation of Roundup® 360 SL, widely used, nonselective herbicide and its main constituents, glyphosate (PMG), equimolar (1:1) isopropylamine salt of glyphosate (GIPA) and isopropylamine (IPA) was examined towards eight aquatic microphotoautotrophs; seven cyanobacterial strains representing either
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service