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Merck
CN

550000

3-Isopropoxypropylamine

≥98%

Synonym(s):

IPOPA

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About This Item

Linear Formula:
(CH3)2CHO(CH2)3NH2
CAS Number:
2906-12-9
Molecular Weight:
117.19
UNSPSC Code:
12352100
PubChem Substance ID:
24879084
EC Number:
220-816-2
MDL number:
MFCD00008220
Assay:
≥98%

Key Documents

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InChI key

VHYUNSUGCNKWSO-UHFFFAOYSA-N

InChI

1S/C6H15NO/c1-6(2)8-5-3-4-7/h6H,3-5,7H2,1-2H3

SMILES string

CC(C)OCCCN

assay

≥98%

refractive index

n20/D 1.4195 (lit.)

bp

78-79 °C/85 mmHg (lit.)

density

0.845 g/mL at 25 °C (lit.)

functional group

amine, ether

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Application

3-Isopropoxypropylamine may be used as a reactant in the preparation of:
  • 1-alcoxyalkyl-5-aryl-4-acyl-3-hydroxy-3-pyrrolin-2-ones
  • 1-(p-sulfamyl)-phenyl-5-oxo-3-pyrrolidine carboxylic acid derivative
  • ethyl 1,4-dihydro-1-(3-isopropoxypropyl)-4-oxo-3-quinolinecarboxylate

General description

3-Isopropoxypropylamine is an aliphatic primary amine.

Legal Information

Product of Arkema Inc.

pictograms

FlameCorrosion
GHS02,GHS05

signalword

Danger

Hazard Classifications

Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1A

Storage Class

3 - Flammable liquids

wgk

WGK 1

flash_point_f

102.2 °F - closed cup

flash_point_c

39 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
01205JO

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Ethyl 1, 4-dihydro-4-oxo-3-quinolinecarboxylates by a tandem addition-elimination-SNAr reaction.
Bunce RA, et al.
Journal of Heterocyclic Chemistry, 48(3), 620-625 (2011)
Itaconic acid derivatives of sulfanilamide.
Paytash PL, et al.
Journal of the American Chemical Society, 74(18), 4549-4552 (1952)
Synthesis and antibacterial activity of 1-alkoxyalkyl-5-aryl-4-acyl-3-hydroxy-3-pyrrolin-2-ones.
Gein VL, et al.
Pharmaceutical Chemistry Journal, 41(4), 208-210 (2007)
Jeffrey A Schneider et al.
Nature communications, 9(1), 4396-4396 (2018-10-26)
New chemical inhibitors of protein-protein interactions are needed to propel advances in molecular pharmacology. Peptoids are peptidomimetic oligomers with the capability to inhibit protein-protein interactions by mimicking protein secondary structure motifs. Here we report the in silico design of a

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