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Merck
CN

15-2380

Isopropylamine

SAJ special grade, ≥99.0%

Synonym(s):

2-Aminopropane

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About This Item

Linear Formula:
(CH3)2CHNH2
CAS Number:
Molecular Weight:
59.11
EC Number:
200-860-9
UNSPSC Code:
12352116
PubChem Substance ID:
Beilstein/REAXYS Number:
605259
MDL number:
Assay:
≥99.0%
Grade:
SAJ special grade
Bp:
33-34 °C (lit.)
Vapor pressure:
9.2 psi ( 20 °C)
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InChI

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

InChI key

JJWLVOIRVHMVIS-UHFFFAOYSA-N

SMILES string

CC(C)N

grade

SAJ special grade

vapor density

2.04 (vs air)

vapor pressure

9.2 psi ( 20 °C)

assay

≥99.0%

autoignition temp.

755 °F

expl. lim.

10.4 %

availability

available only in Japan

dilution

(for analytical testing)

bp

33-34 °C (lit.)

density

0.688 g/mL at 20 °C (lit.)

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signalword

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

3 - Flammable liquids

wgk

WGK 1

flash_point_f

<-13.0 °F - closed cup

flash_point_c

<= -25 °C - closed cup

ppe

Faceshields, Gloves, Goggles

Regulatory Information

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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
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
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.
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
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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