4-(Isopropylamino)butanol
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
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
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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4-(Isopropylamino)butanol(42042-71-7)Related Product Information
- 4,4-DIMETHYL-2-PENTANOL
- Tropine
- 5-chloro-2,3-diphenylpyrazine
- ( 2-{4-[N-(5,6-diphenylpyrazin-2-yl)-N-isopropylamino]butyloxy}acetic acid tert-butylester )
- SELEXIPAG interMediate
- [4-[(5,6-DIPHENYLPYRAZINYL)(1-METHYLETHYL)AMINO]BUTOXY]-ACETIC ACID
- 2,3-DIPHENYLPYRAZINE
- Bromoacetic acid
- 2-T-BUTYL GLYCOLATE
- 5,6-DIPHENYLPYRAZIN-2-OL
- N-(methylsulfonyl)glycine
- 2,3-Dichloro-5,6-diphenylpyrazine
- Acetic acid, 2-[4-[(5,6-diphenyl-2-pyrazinyl)oxy]butoxy]-
- 2-Pyrazinamine, N-(1-methylethyl)-5,6-diphenyl-
- 1-Butanol, 4-[(5,6-diphenyl-2-pyrazinyl)oxy]-
- Acetic acid, 2-[4-[(5,6-diphenyl-2-pyrazinyl)oxy]butoxy]-, 1,1-dimethylethyl ester
- Acetamide, 2-[4-[(1-methylethyl)amino]butoxy]-N-(methylsulfonyl)-
- Acetamide, 2-[4-[(5,6-diphenyl-2-pyrazinyl)(1-methylethyl)amino]butoxy]-