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4-(Isopropylamino)butanol

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4-(Isopropylamino)butanol Basic information

Product Name:
4-(Isopropylamino)butanol
Synonyms:
  • 4-hydroxy-N-isopropylbutan-1-aMine
  • 4-(Isopropylamino)butanol
  • 4-(Isopropylamino)butan-1-ol
  • 4-(propan-2-ylamino)butan-1-ol
  • 1-Butanol, 4-(isopropylamino)-
  • 4-[(1-Methylethyl)amino]-1-butanol
  • 4-(Isopropylamino)butanol>
  • 1-Butanol, 4-[(1-methylethyl)amino]-
CAS:
42042-71-7
MF:
C7H17NO
MW:
131.22
EINECS:
678-583-1
Product Categories:
  • non-prostanoid prostacyclin (PGI2) receptor agonist
Mol File:
42042-71-7.mol
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4-(Isopropylamino)butanol Chemical Properties

Boiling point:
85°C/1mmHg(lit.)
Density 
0.889 g/cm3
refractive index 
1.4480-1.4520
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
form 
clear liquid
pka
15.13±0.10(Predicted)
color 
Colorless to Almost colorless
InChI
InChI=1S/C7H17NO/c1-7(2)8-5-3-4-6-9/h7-9H,3-6H2,1-2H3
InChIKey
IPLWOCGPIGUXOR-UHFFFAOYSA-N
SMILES
C(O)CCCNC(C)C
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Safety Information

RIDADR 
1993
HazardClass 
3
PackingGroup 
III
HS Code 
2922190090
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4-(Isopropylamino)butanol Usage And Synthesis

Chemical Properties

4-(Isopropylamino)butanol is a colorless liquid with an alkaline reaction. It reacts easily with acids and is soluble in water. The boiling point of this substance is 242°C. In the presence of ammonium chloride, the solution becomes acidic.

Uses

4-(Isopropylamino)butanol is used as a solvent for paints, varnishes, and lacquers.

Synthesis

13325-10-5

67-64-1

42042-71-7

The general procedure for the synthesis of 4-(isopropylamino)butanol from 4-amino-1-butanol and acetone was as follows: 200 g of 4-amino-1-butanol (II) was dissolved in a solvent mixture of 400 ml of acetone and 1,000 ml of ethanol, to which was added 20 g of 10% Pd/C catalyst. The hydrogenation reaction was carried out at a hydrogen pressure of 10 atmospheres for 4 to 5 hours. Upon completion of the reaction, the reaction mixture was filtered to remove the catalyst and the filtrate was subsequently concentrated to afford the target compound 4-(isopropylamino)butanol as a colorless oil in quantitative yield.

References

[1] Journal of Medicinal Chemistry, 2015, vol. 58, # 18, p. 7128 - 7137
[2] Patent: WO2017/60827, 2017, A1. Location in patent: Page/Page column 11
[3] Bioorganic and Medicinal Chemistry, 2007, vol. 15, # 21, p. 6692 - 6704
[4] Patent: EP1400518, 2004, A1. Location in patent: Page 21

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