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ETHYL PROPIONYL PYRUVATE

CAS No.
13246-52-1
Chemical Name:
ETHYL PROPIONYL PYRUVATE
Synonyms
ethyl 2,4-dioxohexanoate;AKOS MSC-0253;2,4-dioxohexanoate;ETHYL PROPIONYL PYRUVATE;ETHYL PROPIONYL PYRUVATE USP/EP/BP;2-Oxopentanoic propionic anhydride;2,4-Dioxo-hexanoic acid ethyl ester;Hexanoic acid, 2,4-dioxo-, ethyl ester;ethyl propionyl pyruvate,ethyl 2,4-dioxo hexanoate
CBNumber:
CB6778794
Molecular Formula:
C8H12O4
Molecular Weight:
172.18
MDL Number:
MFCD03265450
MOL File:
13246-52-1.mol
MSDS File:
SDS
Last updated:2025-08-08 17:45:00
Product description Number Pack Size Price
Ethyl 2,4-dioxohexanoate 180231 500mg $240
Ethyl 2,4-dioxohexanoate 180231 1g $300
Ethyl-2,4-dioxohexanoate S701 5g $706
ETHYL PROPIONYL PYRUVATE 95.00% CHM0029540 1G $1070.84
Ethyl 2,4-dioxohexanoate 180231 10g $1600
More product size

ETHYL PROPIONYL PYRUVATE Properties

Boiling point 128-129 °C(Press: 11 Torr)
Density 1.087g/ml
FEMA 3278 | ETHYL 2,4-DIOXOHEXANOATE
storage temp. 2-8°C
pka 6.75±0.46(Predicted)
Appearance Colorless to light yellow Liquid
JECFA Number 603
InChI InChI=1S/C8H12O4/c1-3-6(9)5-7(10)8(11)12-4-2/h3-5H2,1-2H3
InChIKey JGFBKJBAYISHAG-UHFFFAOYSA-N
SMILES C(OCC)(=O)C(=O)CC(=O)CC
LogP 0.35
Substances Added to Food (formerly EAFUS) ETHYL 2,4-DIOXOHEXANOATE
FDA UNII 9064NS087D
EPA Substance Registry System Ethyl 2,4-dioxohexanoate (13246-52-1)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338

ETHYL PROPIONYL PYRUVATE price More Price(21)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Matrix Scientific 180231 Ethyl 2,4-dioxohexanoate 13246-52-1 500mg $240 2021-12-16 Buy
Matrix Scientific 180231 Ethyl 2,4-dioxohexanoate 13246-52-1 1g $300 2021-12-16 Buy
AK Scientific S701 Ethyl-2,4-dioxohexanoate 13246-52-1 5g $706 2021-12-16 Buy
American Custom Chemicals Corporation CHM0029540 ETHYL PROPIONYL PYRUVATE 95.00% 13246-52-1 1G $1070.84 2021-12-16 Buy
Matrix Scientific 180231 Ethyl 2,4-dioxohexanoate 13246-52-1 10g $1600 2021-12-16 Buy
Product number Packaging Price Buy
180231 500mg $240 Buy
180231 1g $300 Buy
S701 5g $706 Buy
CHM0029540 1G $1070.84 Buy
180231 10g $1600 Buy

ETHYL PROPIONYL PYRUVATE Chemical Properties,Uses,Production

Chemical Properties

Colorless liquid

Preparation

From methyl ethyl ketone and ethyl oxalate.

Definition

ChEBI: Ethyl 2,4-dioxohexanoate is a 3-acylpyruvic acid.

Synthesis

Diethyl oxalate

95-92-1

2-Butanone

78-93-3

ETHYL PROPIONYL PYRUVATE

13246-52-1

1. Under nitrogen protection, sodium ethoxide (10 g, 147 mmol) with anhydrous ethanol (65 mL) was added to a dry flask and heated to 70°C to dissolve completely. After cooling to 0 °C, a mixture of 2-butanone (13.16 mL, 147 mmol) and diethyl oxalate (19.96 mL, 147 mmol) was slowly added dropwise and subsequently warmed to room temperature. The reaction mixture was stirred for 1 hour and then heated to 80°C for 45 minutes. Cooled to room temperature and concentrated under reduced pressure to remove the solvent. The residue was dissolved in water (200 mL) and ethyl acetate (3 x 70 mL) to separate the organic phase. The aqueous phase was acidified to pH 2 with dilute sulfuric acid and extracted with ether (3×50 mL), the organic phases were combined, dried with anhydrous sodium sulfate, and concentrated under reduced pressure to give ethyl 2,4-dioxohexanoate as an amber colored oil 16.7 g (66% yield). Mass spectrum (CI) m/z: 173 (M+H)+. 2. Ethyl 2,4-dioxohexanoate (11.22 g, 65.15 mmol) was mixed with hydroxylamine hydrochloride (13.58 g, 195.5 mmol) in ethanol (200 mL) and heated to reflux for 1.5 hours. After cooling, the solvent was removed by concentration under reduced pressure. The residue was partitioned with water (150 mL) and ethyl acetate (2 x 150 mL), and the organic phases were combined, dried with anhydrous magnesium sulfate, and concentrated under reduced pressure to give an amber-colored oil (10.57 g). The crude product was purified by silica gel column chromatography (400 g silica gel, 20% ethyl acetate/hexane elution), the target fractions were combined, and concentrated under reduced pressure to afford ethyl 5-ethylisoxazole-3-carboxylate as a light-colored oil 8.95 g (81% yield). High resolution mass spectrometry (ESI) calculated value C8H11NO3+H: 170.0817, measured value 170.0824 (M+H)+. 3. An aqueous solution (35 mL) of sodium hydroxide (10.9 g, 273 mmol) was added to a solution of ethyl 5-ethylisoxazole-3-carboxylate (11.6 g, 68 mmol) in methanol (70 mL), and stirred at room temperature for 3 hours. The methanol was removed by concentration under reduced pressure, acidified with concentrated hydrochloric acid to pH 2. The acidic aqueous phase was extracted with dichloromethane (2 x 150 mL), then with 10% methanol/ dichloromethane (4 x 150 mL), the organic phases were combined, dried with anhydrous magnesium sulfate, and concentrated under reduced pressure to give 5.65 g of 5-ethylisoxazole-3-carboxylic acid as a white solid (58% yield). Mass spectrum (CI) m/z: 142 (M+H)+. 4. 5-Ethylisoxazole-3-carboxylic acid (1.41 g, 10 mmol) was dissolved in benzene (30 mL), oxalyl chloride (3.46 mL, 40 mmol) was added, and heated to reflux for 2 hours. After cooling, the solvent was removed by concentration under reduced pressure and the residue was azeotroped with dichloromethane to remove residual benzene. The resulting chloride was dissolved in acetone (15 mL), an aqueous solution of sodium azide (1.95 g, 30 mmol) was added (7 mL) and stirred vigorously for 1 hour. The acetone was removed by concentration under reduced pressure, and the residue was ground with water, filtered, washed with water and dried under vacuum to give 1.46 g of 5-ethylisoxazole-3-carbonyl azide as a white solid (88% yield).1H NMR (CDCl3,400MHz): δ1.34,2.85,6.46ppm. 5. 5-Ethylisoxazole-3-carbonyl azide (294 mg, 1.8 mmol) was mixed with 5-chloro-2,4-dimethoxyaniline (332 mg, 1.8 mmol) in anhydrous acetonitrile (20 mL) and heated to 70 °C for 20 h. The reaction was carried out at 70 °C for 20 min. After cooling, the solid was collected by filtration, washed with ether and dried under vacuum to give white solid Example 627 448 mg (78% yield). High resolution mass spectrometry (ESI) calculated value C14H16N3O4Cl+H: 326.0907, measured value 326.0909 (M+H)+.

References

[1] Synthetic Communications, 2013, vol. 43, # 1, p. 110 - 117
[2] Journal of Agricultural and Food Chemistry, 2012, vol. 60, # 6, p. 1470 - 1479
[3] Chinese Chemical Letters, 2016, vol. 27, # 4, p. 566 - 570
[4] Patent: US2003/236287, 2003, A1. Location in patent: Page 47, 48
[5] Monatshefte fur Chemie, 2003, vol. 134, # 9, p. 1221 - 1227

ETHYL PROPIONYL PYRUVATE Preparation Products And Raw materials

Global( 106)Suppliers
Supplier Tel Email Country ProdList Advantage
Capot Chemical Co.,Ltd.
+86-(0)57185586718; +8613336195806 sales@capot.com China 29735 60
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ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 33024 60
career henan chemical co
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Hubei Jusheng Technology Co.,Ltd.
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Changzhou Ditong Chemical Co.,Ltd
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Alchem Pharmtech,Inc.
8485655694 sales@alchempharmtech.com United States 63687 58
Jinan Liheng Biotechnology Co., Ltd.
15865262812 info@lihengpharm.com CHINA 938 58
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418671 +8618949823763 sales@tnjchem.com China 34563 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 20284 58

View Lastest Price from ETHYL PROPIONYL PYRUVATE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
ETHYL PROPIONYL PYRUVATE pictures 2019-09-02 ETHYL PROPIONYL PYRUVATE
13246-52-1
US $7.00 / KG 1KG 99% JD 673 Career Henan Chemical Co

ETHYL PROPIONYL PYRUVATE Spectrum

ETHYL PROPIONYL PYRUVATE AKOS MSC-0253 ethyl 2,4-dioxohexanoate 2,4-dioxohexanoate Hexanoic acid, 2,4-dioxo-, ethyl ester ethyl propionyl pyruvate,ethyl 2,4-dioxo hexanoate 2,4-Dioxo-hexanoic acid ethyl ester 2-Oxopentanoic propionic anhydride ETHYL PROPIONYL PYRUVATE USP/EP/BP 13246-52-1 246-52-1