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Merck
CN

59330

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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
57651680
EC Number:
200-860-9
Beilstein/REAXYS Number:
605259
MDL number:
MFCD00008082
Assay:
≥97.0% (GC)
Form:
liquid

Key Documents

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InChI key

JJWLVOIRVHMVIS-UHFFFAOYSA-N

InChI

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

SMILES string

CC(C)N

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 %

Quality Level

200

impurities

≤3% water

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

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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

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCN6870
BCCM3754
BCCH8953
BCCL4108
BCCK9146

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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
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.
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