36701-01-6

Basic information

• Product Name: Furfuryl pentanoate
• Synonyms: FURFURYL PENTANOATE;FURFURYL VALERATE;FEMA 3397;ALPHA-FURFURYL PENTANOATE;2-FURFURYL PENTANOATE;Pentanoicacid,2-furanylmethylester;FURFURYL PENTANOATE 97+%;furfuryl pentanoat
• CAS NO: 36701-01-6
• Molecular Formula: C₁₀H₁₄O₃
• Molecular Weight: 182.22
• EINECS: 253-160-0
• Product Categories: ester Flavor
• Mol File: 36701-01-6.mol

Chemical Properties

• Boiling Point: 82-83 °C1 mm Hg(lit.)
• Flash Point: 209 °F
• Appearance: /
• Density: 1.028 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.0668mmHg at 25°C
• Refractive Index: n20/D 1.46(lit.)
• CAS DataBase Reference: Furfuryl pentanoate(CAS DataBase Reference)
• NIST Chemistry Reference: Furfuryl pentanoate(36701-01-6)
• EPA Substance Registry System: Furfuryl pentanoate(36701-01-6)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 36701-01-6(Hazardous Substances Data)

Usage

Uses

Used in Food and Beverage Industry:
Furfuryl pentanoate is used as a flavoring substance for inducing fruit-like tastes, particularly pineapple, in food and beverage products.
Used in Cosmetic Industry:
Furfuryl pentanoate is used as a fragrance ingredient in various cosmetic products, contributing to their pleasant and appealing scents.
Safety Considerations:
Despite its applications, furfuryl pentanoate must be handled with care due to its potential hazards and toxicity.

InChI:InChI=1/C10H14O3/c1-2-3-6-10(11)13-8-9-5-4-7-12-9/h4-5,7H,2-3,6,8H2,1H3

Upstream product

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• 79246-43-8 3-valeroyloxymethylpyridazine 1-oxide 
• 100-66-3 methoxybenzene 
• 110-83-8 cyclohexene 
• 67-47-0 5-hydroxymethyl-2-furfuraldehyde 
• 542-69-8 1-iodo-butane 

Relevant articles and documents

HMF and furfural: Promising platform molecules in rhodium-catalyzed carbonylation reactions for the synthesis of furfuryl esters and tertiary amides

A biomass involved rhodium-catalyzed carbonylative synthesis of furfuryl esters and tertiary amides has been developed. 5-Hydroxymethylfurfural (HMF) was used as both substrate and CO surrogate for the first time in a carbonylation reaction, and both alkyl and aryl iodides were tolerated well to afford the desired furfuryl esters in moderate to good yields. In addition, furfural was also utilized as a CO source for the synthesis of tertiary amides. A variety of tertiary amides were obtained in moderate to excellent yields with good functional groups compatibility. Notably, tertiary amines were used as the amine source through a C[sbnd]N bond cleavage pathway in the absence of additional oxidant.

A STUDY ON THE TRANSITION STATE IN THE PHOTOOXYGENATIONS BY AROMATIC AMINE N-OXIDES

Oxygen-atom transfer process in the photolysis of aromatic amine N-oxides was suggested to involve the primary oxygen-atom elimination from N-oxides to give "oxene" followed by its reactions with the oxygen-acceptors.