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59330

Sigma-Aldrich

Isopropylamine

≥97.0% (GC)

Synonym(s):

2-Aminopropane

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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

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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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM3754
BCCH8953
BCCL4108
BCCK9146
BCCC6592

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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
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
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
Katrijn De Klerck et al.
Journal of chromatography. A, 1234, 72-79 (2011-12-07)
In chiral supercritical fluid chromatography (SFC), mobile-phase additives are often used to improve enantioseparations and peak shapes. An acidic or basic additive is chosen, depending on the nature of the compound. This work highlights the simultaneous use of the acidic
Bambang Veriansyah et al.
Journal of hazardous materials, 124(1-3), 119-124 (2005-06-09)
Supercritical water oxidation can effectively destroy a large variety of high-risk wastes resulting from munitions demilitarization and complex industrial chemical. An important design consideration in the development of supercritical water oxidation is the information on the oxidation rate. In this
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