94089-18-6

Basic information

• Product Name: 4-[(3-acetoxypropyl)amino]-2,2-dimethyl-4-oxobutane-1,3-diyl diacetate
• Synonyms: 4-[(3-acetoxypropyl)amino]-2,2-dimethyl-4-oxobutane-1,3-diyl diacetate;PANTHENYL TRIACETATE;(R)-2,4-Bis(acetyloxy)-N-[3-(acetyloxy)propyl]-3,3-dimethylbutanamide
• CAS NO: 94089-18-6
• Molecular Formula: C15H25NO7
• Molecular Weight: 331.3615
• EINECS: 302-118-0
• Mol File: 94089-18-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 471.9°Cat760mmHg
• Flash Point: 239.2°C
• Appearance: /
• Density: 1.131g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.461
• CAS DataBase Reference: 4-[(3-acetoxypropyl)amino]-2,2-dimethyl-4-oxobutane-1,3-diyl diacetate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-[(3-acetoxypropyl)amino]-2,2-dimethyl-4-oxobutane-1,3-diyl diacetate(94089-18-6)
• EPA Substance Registry System: 4-[(3-acetoxypropyl)amino]-2,2-dimethyl-4-oxobutane-1,3-diyl diacetate(94089-18-6)

Safety Data

• Hazardous Substances Data: 94089-18-6(Hazardous Substances Data)

Usage

Uses

panthenyl triacetate is a panthotenic acid derivative with vitamin B activity.

InChI:InChI=1/C15H25NO7/c1-10(17)21-8-6-7-16-14(20)13(23-12(3)19)15(4,5)9-22-11(2)18/h13H,6-9H2,1-5H3,(H,16,20)

Upstream product

• 81-13-0 pantothenol 
• 108-24-7 acetic anhydride 
• 108-05-4 vinyl acetate 
• 50584-68-4 panthenol 

Relevant articles and documents

MULTIBIOTIC AGENTS AND METHODS OF USING THE SAME

Multibiotic agents are disclosed. The multibiotic agents may contain two or more moieties linked through bonds cleavable in vivo. The bonds cleavable in vivo can be ester bonds, amide bonds, azo bonds, glycosidic bonds, carbonate linkers, or carbamate linkers. The moieties can be alcohol cores, amine cores, and/or acyls. Also disclosed are compositions containing multibiotic agents and methods of using the multibiotic agents.

Selective synthesis of panthenyl esters by a kinetically controlled enzymatic process

Panthenyl esters (panthenyl monoacetate and panthenyl diacetate) were synthesized in high yields (≈100%) by a kinetic reaction control using a commercial immobilized Candida Antarctica lipase B (Novozyme 435) in acetonitrile. The enzyme showed excellent synthetic activity, regioselectivity, and operational stability under the conditions used.