16224-33-2

Basic information

• Product Name: 1-Butoxy-3-chloro-2-propanol
• Synonyms: 1-Butoxy-3-chloro-2-propanol
• CAS NO: 16224-33-2
• Molecular Formula: C₇H₁₅ClO₂
• Molecular Weight: 166.67
• Mol File: 16224-33-2.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 234.9°C (rough estimate)
• Flash Point: 98.1°C
• Appearance: /
• Density: 1.0732 (rough estimate)
• Vapor Pressure: 0.00745mmHg at 25°C
• Refractive Index: 1.4268 (estimate)
• PKA: 13.27±0.20(Predicted)
• CAS DataBase Reference: 1-Butoxy-3-chloro-2-propanol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Butoxy-3-chloro-2-propanol(16224-33-2)
• EPA Substance Registry System: 1-Butoxy-3-chloro-2-propanol(16224-33-2)

Safety Data

• Hazardous Substances Data: 16224-33-2(Hazardous Substances Data)

Usage

General Description

1-Butoxy-3-chloro-2-propanol is a chemical compound used in a variety of industrial and commercial applications. It is often utilized as a solvent in cleaning products, as well as in the production of paints, coatings, and adhesives. This chemical is known for its strong cleaning and degreasing properties, making it a valuable ingredient in many industrial and household cleaning formulations. However, it is important to note that 1-Butoxy-3-chloro-2-propanol may pose health risks if not handled properly, as it can be irritating to the skin, eyes, and respiratory system. Therefore, it is essential to follow safety precautions and guidelines when working with this chemical.

InChI:InChI=1/C7H15ClO2/c1-2-3-4-10-6-7(9)5-8/h7,9H,2-6H2,1H3

Upstream product

• 106-89-8 epichlorohydrin 
• 71-36-3 butan-1-ol 
• 2426-08-6 glycidyl n-butyl ether 
• 64-19-7 acetic acid 

Downstream Products

• 32972-04-6 1-diethylamino-3-butoxy-2-propanole 
• 26798-89-0 Bis-(2-butoxy-1-chloromethyl-ethoxy)-diphenyl-silane 
• 10461-30-0 1-Butoxy-3-[2-(2-methoxy-phenoxy)-ethylamino]-propan-2-ol 
• 67441-96-7 1-(3-butoxy-2-hydroxy-propyl)-5-ethyl-5-phenyl-pyrimidine-2,4,6-trione 
• 98451-40-2 3-n-butoxy-1,2-propanediol 
• 105996-48-3 [2-(4-Bromo-phenyl)-2-oxo-ethyl]-(3-butoxy-2-hydroxy-propyl)-dimethyl-ammonium; bromide 
• 105996-38-1 dl-1-Butoxy-2-hydroxy-3-dimethylaminopropane 
• 32338-77-5 3-butoxypropyl-1,2-episulfide 
• 2426-08-6 glycidyl n-butyl ether 
• 53146-45-5 1-allyloxy-3-butoxypropan-2-ol 
• 26798-85-6 C₂₇H₄₇Cl₃O₆Si 

Relevant articles and documents

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1,3,2,4-diazadiphosphetidine-based phosphazane oligomers as source of P(III) atom economy reagents: Conversion of epoxides to vic -haloalcohols, vic -dihalides, and alkenes in the presence of halogen sources

1,3,2,4-Diazadiphosphetidines (P1-P3), as easily prepared, stable, and heterogeneous P(III) compounds, were used for the efficient conversion of epoxides to vic-halohydrins, vic-dihalides, or alkenes in the presence of different halogen sources in CH3CN. Of these phosphazanes, P3 is most suitable and contains 4 phosphorous atoms with the advantage of having greater atom economy and its phosphorus oxide byproduct can be easily separated from the reaction mixture by simple filtration. The nitrogen atoms in this molecule can also act as acid scavengers in the reaction.

Synthesis of 1-alkoxy-3-N-succinimido-2-propanols

Procedures for preparing 1-alkoxy-3-chloro-2-propanols, with their subsequent transformation to 1-alkoxy-N-succinimido-2-propanols, were developed.