60278-95-7

Basic information

• Product Name: 3-(butylamino)propane-1,2-diol
• Synonyms: 3-(butylamino)propane-1,2-diol;3-(Butylamino)-1,2-propanediol
• CAS NO: 60278-95-7
• Molecular Formula: C₇H₁₇NO₂
• Molecular Weight: 147.21538
• EINECS: 262-142-1
• Mol File: 60278-95-7.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 277.8°C at 760 mmHg
• Flash Point: 121°C
• Appearance: /
• Density: 0.992g/cm³
• Vapor Pressure: 0.000545mmHg at 25°C
• Refractive Index: 1.466
• CAS DataBase Reference: 3-(butylamino)propane-1,2-diol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(butylamino)propane-1,2-diol(60278-95-7)
• EPA Substance Registry System: 3-(butylamino)propane-1,2-diol(60278-95-7)

Safety Data

• Hazardous Substances Data: 60278-95-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C7H17NO2/c1-2-3-4-8-5-7(10)6-9/h7-10H,2-6H2,1H3

Upstream product

• 556-52-5 oxiranyl-methanol 
• 109-73-9 N-butylamine 

Relevant articles and documents

1,2-Diol type polyol derivative compound and preparation method thereof and anti-microbial composition containing it

The present invention relates to a polyol derivative compound having a 1,2-diol structure represented by chemical formula 1, a method of preparing the same, and an anti-microbial composition containing the compound as an active ingredient. In the chemical formula: R1 is nitrogen (N) or sulfur (S); and R2 is OH or C2 alkyl. According to the present invention, the polyol derivative compound having a 1,2-diol structure represented by the chemical formula 1 exhibits excellent anti-microbial activities better than 1,2-hexanediol, which is known to have the best anti-microbial activity among polyols, thereby being effectively used as a preservative for a food product, a medicine, a cosmetic, and the like to prevent spoilage caused by microorganisms.COPYRIGHT KIPO 2019

The reaction of sulfamic acid derivatives with epoxides. 4. Hydrolysis of 3-chloro-2-hydroxypropylsulfamates

Under basic hydrolysis conditions 3-chloro-2-hydroxypropylsulfamates transform into 2,3-dihydroxypropylsulfamates. Acidic hydrolysis of the latter leads to 3-alkylaminopropane-1,2-diols.