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471291

Sigma-Aldrich

Isopropylamine

≥99.5%

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/REAXYS Number:
605259
EC Number:
200-860-9
MDL number:
MFCD00008082
UNSPSC Code:
12352100
PubChem Substance ID:
24870715
NACRES:
NA.22

vapor density

2.04 (vs air)

Quality Level

200

vapor pressure

9.2 psi ( 20 °C)

assay

≥99.5%

form

liquid

autoignition temp.

755 °F

expl. lim.

10.4 %

impurities

≤0.1% water

color

APHA: ≤50

refractive index

n20/D 1.374 (lit.)

bp

33-34 °C (lit.)

density

0.688 g/mL at 20 °C (lit.)

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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General description

Isopropylamine (i-PrNH2), a primary mine, is a urinary metabolite of propranolol.

Application

Isopropylamine was used in the following studies:
  • Preparation of enantiomerically pure (R and S)- acebutolol.
  • As template during the hydrothermal synthesis of SAPO materials.
  • Synthesis of bis(salicylaldiminate)nickel(II) complexes.
  • Preparation of hydrated, microporous aluminum phosphate AlPO-14.

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_germany

WGK 1

flash_point_f

<-13.0 °F - closed cup

flash_point_c

<= -25 °C - closed cup

ppe

Faceshields, Gloves, Goggles

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Certificates of Analysis (COA)

Lot/Batch Number
MKCQ3151
MKCM6934
BCCC6592
MKCK8067
BCBZ3058

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Isopropylamine, a biologically active deamination product of propranolol in dogs: identification of deuterated and unlabeled isopropylamine by gas chromatography-mass spectrometry.
T Walle et al.
The Journal of pharmacology and experimental therapeutics, 183(3), 508-512 (1972-12-01)
Huaixin Yang et al.
The journal of physical chemistry. B, 109(10), 4464-4469 (2006-07-21)
Differential scanning calorimetry of the hydrated, microporous aluminum phosphate AlPO-14 shows two distinct water losses between room temperature and 120 degrees C, indicating the presence of two types of water in the solid. Multiple-quantum magic angle spinning (MQMAS) (27)Al NMR
Linga Banoth et al.
Chirality, 27(6), 382-391 (2015-05-16)
A new chemoenzymatic route is reported to synthesize acebutolol, a selective β1 adrenergic receptor blocking agent in enantiopure (R and S) forms. The enzymatic kinetic resolution strategy was used to synthesize enantiopure intermediates (R)- and (S)-N-(3-acetyl-4-(3-chloro-2-hydroxypropoxy)phenyl)butyramide from the corresponding racemic
Ethylene oligomerization by novel catalysts based on bis (salicylaldiminate) nickel (II) complexes and organoaluminum co-catalysts.
Carlini C, et al.
Applied Catalysis A: General, 231(1), 307-320 (2002)
On the possibility of incorporating Mn (II) and Cr (III) in SAPO-34 in the presence of isopropylamine as a template.
Rajic N, et al.
Zeolites, 13(4), 384-387 (1993)
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