Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

45945

Supelco

Isopropylamine

anhydrous, analytical standard

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:
41116107
PubChem Substance ID:
329757019
NACRES:
NA.24

grade

analytical standard

vapor density

2.04 (vs air)

vapor pressure

9.2 psi ( 20 °C)

autoignition temp.

755 °F

quality

anhydrous

shelf life

limited shelf life, expiry date on the label

expl. lim.

10.4 %

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.374 (lit.)

bp

33-34 °C (lit.)

density

0.688 g/mL at 20 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care

format

neat

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

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Recommended products

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

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
BCCM0005
BCCL2209
BCCK4254
BCCH6119
BCCF5389

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
Hsin-Ling Lee et al.
Clinical toxicology (Philadelphia, Pa.), 47(7), 651-658 (2009-08-12)
Most of the glyphosate-surfactant herbicides (GlySH) are formulated commercial products containing isopropylamine (IPA) salt of glyphosate (IPAG), variable amount of a surfactant, and water. Although glyphosate is only slightly toxic to rats, ingestion of GlySH may lead to severe effects
Karim Engelmark Cassimjee et al.
Chemical communications (Cambridge, England), 46(30), 5569-5571 (2010-05-13)
Enantiopure chiral amines synthesis using omega-transaminases is hindered by an unfavourable equilibrium, but when using isopropylamine as the amine donor the equilibrium can be completely displaced by using a specific dehydrogenase in situ for removal of formed acetone.
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