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Butyl levulinate

CAS No.
2052-15-5
Chemical Name:
Butyl levulinate
Synonyms
NBL;PENTANOIC ACID, 4-OXO-, BUTYL ESTER;FEMA 2207;FEMA 22073;Butyl levulite;BUTYLLAEVULATE;Butyl Levuhnate;Butyl leulinate;butyllaevulinate;BUTYL LEVULINATE
CBNumber:
CB5778065
Molecular Formula:
C9H16O3
Molecular Weight:
172.22
MDL Number:
MFCD00009449
MOL File:
2052-15-5.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-09-12 14:30:55

Butyl levulinate Properties

Boiling point 106-108 °C5.5 mm Hg(lit.)
Density 0.974 g/mL at 25 °C(lit.)
vapor pressure 5Pa at 25℃
FEMA 2207 | BUTYL LEVULINATE
refractive index n20/D 1.427(lit.)
FLAVIS Number 09.436 | Butyl 4-oxovalerate
Flash point 197 °F
storage temp. 2-8°C
form clear liquid
color Colorless to Almost colorless
Specific Gravity 0.974
Odor at 100.00 %. fruity herbal waxy caramel savory
Odor Type herbal
biological source synthetic
Water Solubility Slightly soluble in water.
JECFA Number 608
Cosmetics Ingredients Functions SOLVENT
SKIN CONDITIONING - EMOLLIENT
PERFUMING
InChI 1S/C9H16O3/c1-3-4-7-12-9(11)6-5-8(2)10/h3-7H2,1-2H3
InChIKey ISBWNEKJSSLXOD-UHFFFAOYSA-N
SMILES CCCCOC(=O)CCC(C)=O
LogP 1.435 at 20℃
Surface tension 31.37mN/m at 293.15K
Substances Added to Food (formerly EAFUS) BUTYL LEVULINATE
FDA 21 CFR 172.515
CAS DataBase Reference 2052-15-5(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII OI56208RTB
NIST Chemistry Reference Pentanoic acid, 4-oxo-, butyl ester(2052-15-5)
EPA Substance Registry System Butyl levulinate (2052-15-5)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
PPE Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
Hazard Codes  Xi
Safety Statements  24/25
WGK Germany  2
RTECS  OI1695000
Hazard Note  Irritant
TSCA  TSCA listed
HS Code  29183000
Storage Class 10 - Combustible liquids
Hazard Classifications Eye Irrit. 2
Skin Irrit. 2
REACH Registrations Active
NFPA 704
2
0 0

Butyl levulinate price More Price(20)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical L0138 Butyl Levulinate >98.0%(GC) 2052-15-5 25mL $39 2026-04-30 Buy
TCI Chemical L0138 Butyl Levulinate >98.0%(GC) 2052-15-5 500mL $239 2026-04-30 Buy
Biosynth CAA05215 Butyl levulinate 2052-15-5 100g $900 2026-06-04 Buy
Biosynth CAA05215 Butyl levulinate 2052-15-5 1000g $900 2026-06-04 Buy
Biosynth CAA05215 Butyl levulinate 2052-15-5 500g $900 2026-06-04 Buy
Product number Packaging Price Buy
L0138 25mL $39 Buy
L0138 500mL $239 Buy
CAA05215 100g $900 Buy
CAA05215 1000g $900 Buy
CAA05215 500g $900 Buy

Butyl levulinate Chemical Properties, Uses, Production

Aroma

Sweet and slightly pungent-caramellic odor with fruity undertones. Overall warm and almost herbaceous with some similarity to Valerolactone. Mild, sweet, caramellic-herbaceous taste.

Chemical Properties

Butyl levulinate has a sweet and slightly pungent caramellic odor with fruity undertones; mild sweet caramellicherbaceous taste; bitter taste.

Uses

Butyl 4-Oxopentanoate is used in preparation and application of magnetic nano-solid acid catalyst iron oxide-polydopamine-sulfonic acid

Uses

Butyl levulinate can be used in flavor compositions for imitation Butter, Rum, and in various fruit flavors, "Tutti-frutti", etc. Concentration is usually mere traces (a few ppm. ) in the finished product.

Production Methods

Butyl levulinate can be produced by direct esterificalion of n-Butyl alcohol with Levulinic acid.

Definition

ChEBI: Butyl levulinate is an oxo carboxylic acid.

Synthesis Reference(s)

Tetrahedron Letters, 31, p. 3063, 1990 DOI: 10.1016/S0040-4039(00)89026-7

Flammability and Explosibility

Not classified

64-18-6
123-76-2
71-36-3
592-84-7
2052-15-5
Synthesis of Butyl levulinate from Formic acid and Levulinic acid and 1-Butanol

Butyl levulinate Preparation Products And Raw materials

Raw materials

Preparation Products

Global Suppliers ( 229)
Supplier Tel Email Country ProdList Advantage
Langfang Hawk Technology & Development Co., Ltd. 316-2224727 18631652130 fenghe0820@hawk-chinachem.com China 30 58
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Alfa Aesar 400-6106006 saleschina@alfa-asia.com China 30103 84
TCI (Shanghai) Development Co., Ltd. 021-67121386 Sales-CN@TCIchemicals.com China 24512 81
Beijing HwrkChemical Technology Co., Ltd 89508211 18501085097 sales.bj@hwrkchemical.com China 9409 55
Energy Chemical 400-0056266 18918157536; sales8178@energy-chemical.com China 45000 61
Capot Chemical Co., Ltd +86 (0) 571 85 58 67 18 China 18187 66
Adamas Reagent, Ltd. 4006009262 13023226327 hmj@titansci.com China 14098 59
XiaoGan ShenYuan ChemPharm co,ltd 15527621225; 15527621225 1791901229@qq.com China 6722 52
Beijing Isomersyn Technology CO;LTD 010-82954736 13391601435 sales@isomersyn.com China 3294 57

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Butyl levulinate, 98% 500ML Levulinic Acid Butyl Ester 4-Oxovaleric Acid Butyl Ester Butyl 4-Oxovalerate Butyl 4-oxopentanoate Butyl laevulinate butyl4-oxopentanoate butyllaevulinate Levulinic acid, butyl ester levulinicacid,butylester n-Butyl laevulinate n-butyllaevulinate LEVULINIC ACID N-BUTYL ESTER BUTYL LEVULINATE BUTYL 4-OXOVALERATE FEMA 2207 FEMA 22073 4-Oxo-pentanoic acid butyl ester 4-OXO-N-VALERIC ACID N-BUTYL ESTER 4-KETO-N-VALERIC ACID N-BUTYL ESTER N-BUTYL LEVULINATE Butyl levulinate 98% Butyl Levuhnate Butyl levulite 4-Ketopentanoic acid butyl ester 4-ketopentanoicacidbutylester 4-oxo-pentanoicacibutylester 2,4,5-Trimethoxyamphetamine Hydrochloride n-butyl 4-oxopentanoate BUTYL LEVULINATE 97+% BUTYLLAEVULATE N-Butyl-4-oxopentanoat 4-Oxovaleric Acid Butyl Ester 3-Acetylpropanoic acid butyl ester Butyl levulinate,98% Butyl leulinate ButylLevulinate> Butyl levulinate USP/EP/BP NBL PENTANOIC ACID, 4-OXO-, BUTYL ESTER 2052-15-5 2052-12-5 C2H5COCH22COOC4H9 CH3COCH2CH2CO2CH23CH3 Carbonyl Compounds C8 to C9 Building Blocks Organic Building Blocks Esters Flavors and Fragrances Building Blocks C8 to C9 Carbonyl Compounds Chemical Synthesis Organic Building Blocks Pharmaceutical Intermediates C8 to C9 Carbonyl Compounds Esters A-B