Skip to Content
Merck
All Photos(1)

Documents

W342807

Sigma-Aldrich

Ethyl 3-hydroxybutyrate

≥97%, FG

Synonym(s):

grape butyrate

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3CH(OH)CH2COOC2H5
CAS Number:
Molecular Weight:
132.16
FEMA Number:
3428
Beilstein:
1446190
EC Number:
Council of Europe no.:
10596
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
9.522
NACRES:
NA.21

biological source

synthetic

Quality Level

grade

FG
Fragrance grade
Halal
Kosher

Agency

follows IFRA guidelines

reg. compliance

EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002

Assay

≥97%

refractive index

n20/D 1.42 (lit.)

bp

170 °C (lit.)

density

1.017 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

no known allergens

Organoleptic

grape; green; fruity

SMILES string

CCOC(=O)CC(C)O

InChI

1S/C6H12O3/c1-3-9-6(8)4-5(2)7/h5,7H,3-4H2,1-2H3

InChI key

OMSUIQOIVADKIM-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Ethyl 3-hydroxybutyrate is one of the main aroma components of wine. It occurs naturally in fruits such as pineapple, tamarillo fruit, caja fruit and naranjilla fruit.

Application


  • Deciphering the immobilization of lipases on hydrophobic wrinkled silica nanoparticles.: This study explores the immobilization of lipases on hydrophobic wrinkled silica nanoparticles, highlighting the potential of these nanoparticles in biocatalysis applications, which can be critical for biochemical synthesis processes involving compounds like Ethyl 3-hydroxybutyrate. (Pota et al., 2024).

  • Exploring the Therapeutic Potential of Ethyl 3-Hydroxybutyrate in Alleviating Skeletal Muscle Wasting in Cancer Cachexia.: This research investigates the therapeutic effects of Ethyl 3-hydroxybutyrate in reducing muscle wasting in cancer patients, demonstrating its potential biochemical applications in medical treatments. (Zhou et al., 2023).

  • High-Pressure Depolymerization of Poly(lactic acid) (PLA) and Poly(3-hydroxybutyrate) (PHB) Using Bio-Based Solvents: A Way to Produce Alkyl Esters Which Can Be Modified to Polymerizable Monomers.: This study explores the depolymerization of biopolymers using bio-based solvents, resulting in alkyl esters like Ethyl 3-hydroxybutyrate, highlighting its applications in sustainable biochemical processes. (Jašek et al., 2022).

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

170.6 °F - closed cup

Flash Point(C)

77 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Identification of additional pineapple volatiles
Takeoka GR, et al.
Journal of Agricultural and Food Chemistry, 39(10), 1848-1851 (1991)
Fast analysis of important wine volatile compounds: Development and validation of a new method based on gas chromatographic?flame ionisation detection analysis of dichloromethane microextracts.
Ortega C, et al.
Journal of Chromatography A, 923(1), 205-214 (2001)
Volatiles from naranjilla fruit (Solanum quitoense Lam.). GC/MS analysis and sensory evaluation using sniffing GC
Brunke EJ, et al.
Journal of Agricultural and Food Chemistry, 37(3), 746-748 (1989)
Volatile constituents from Tamarillo (Cyphomandra betacea Sendtn.) fruit.
Torrado A, et al.
Flavour and Fragrance Journal, 10(6), 349-354 (1995)
Identification of volatile components of caja fruit (Spondias lutea L.) and chiral analysis of 3?hydroxy aliphatic esters.
Allegrone G & Barbeni M.
Flavour and Fragrance Journal, 7(6), 337-342 (1992)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service