550000
3-Isopropoxypropylamine
≥98%
Synonym(s):
IPOPA
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
(CH3)2CHO(CH2)3NH2
CAS Number:
Molecular Weight:
117.19
UNSPSC Code:
12352100
PubChem Substance ID:
EC Number:
220-816-2
MDL number:
Assay:
≥98%
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
General description
3-Isopropoxypropylamine is an aliphatic primary amine.
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
Legal Information
Product of Arkema Inc.
signalword
Danger
hcodes
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
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Itaconic acid derivatives of sulfanilamide.
Paytash PL, et al.
Journal of the American Chemical Society, 74(18), 4549-4552 (1952)
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)
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
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service