3-ethyl-2-hydroxy-2-cyclopenten-1-one

Available forms:White Crystalline powder

pd_proNo:466562-dc98e0d6-3b92-4488-bd1f-a9ec3a4887ed

pd_productuse:

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Detailed introduction

Factory Sells Best Quality 3-ethyl-2-hydroxy-2-cyclopenten-1-one 21835-01-8 with GMP standards

  • Molecular Formula:C7H10O2
  • Molecular Weight:126.155
  • Appearance/Colour:White Crystalline powder 
  • Vapor Pressure:0.00204mmHg at 25°C 
  • Melting Point:39.0 to 43.0 °C 
  • Refractive Index:n20/D 1.476  
  • Boiling Point:258.3 °C at 760 mmHg 
  • PKA:9.17±0.20(Predicted) 
  • Flash Point:107.2 °C 
  • PSA:37.30000 
  • Density:1.156 g/cm3 
  • LogP:1.57140 

3-Ethyl-2-hydroxy-2-cyclopenten-1-one(Cas 21835-01-8) Usage

Preparation

From 5-methyl-3,5-dicarbethoxy-2-cyclopen-ten-2-ol-one and phosphoric acid; by a patented process; also from dimethyl adipate.

Aroma threshold values

Aroma characteristics at 0.5%: sweet, brown, caramellic, maple, brown sugar, rum, whiskey, furanone.

Taste threshold values

A threshold value of 5 ppm, similar to the 3-methyl analog, has been determined by comparative sensory evaluation. Taste characteristics at 12 ppm: sweet, jamy, fruity, brown, toasted, maple, nutty

General Description

3-Ethyl-2-hydroxy-2-cyclopenten-1-one is formed by thermal degradation of ascorbic acid. It is an aroma compound formed from the reactions of L-ascorbic acid with L-threonine/L-serine at different pH values.

InChI:InChI=1/C7H10O2/c1-2-5-3-4-6(8)7(5)9/h9H,2-4H2,1H3

21835-01-8 Relevant articles

High yield "one-pot" synthesis of 2-hydroxy-3-methylcyclopent-2-en-1-one and related compounds

Strunz, George M.,Lal, G. Sankar

, p. 572 - 573 (1982)

A convenient "one-pot" modification of a...

-

Barco,A. et al.

, p. 104 - 105 (1975)

-

The effect of pH on the formation of aroma compounds produced by heating a model system containing l-ascorbic acid with l-threonine/l-serine

Yu, Ai-Nong,Zhang, Ai-Dong

experimental part, p. 214 - 219 (2011/12/14)

The identification of aroma compounds, f...

Reactions of 1,2-bis(trimethylsilyloxy)cycloalkenes with the diethyl acetals of aldehydes

Gao, Fuye,Burnell, D. Jean

, p. 356 - 359 (2007/10/03)

Lewis acid-mediated reactions of 1,2-bis...

Acetoacetic acid ester derivatives for the manufacture of α-hydroxycarbonyl compounds

-

, (2008/06/13)

The invention is concerned with a novel ...

21835-01-8 Process route

L-serin
56-45-1,83245-15-2

L-serin

ascorbic acid
50-81-7,98966-42-8

ascorbic acid

furfural
98-01-1

furfural

2-Methylpyrazine
109-08-0

2-Methylpyrazine

2,5-dimethyl-pyrazine
123-32-0

2,5-dimethyl-pyrazine

1-benzofurane
271-89-6

1-benzofurane

2,5-diformylfurane
823-82-5,163857-09-8

2,5-diformylfurane

1-furfuryl-pyrrole
1438-94-4

1-furfuryl-pyrrole

2,2'-difurylmethane
1197-40-6

2,2'-difurylmethane

2,4-di-tert-Butylphenol
96-76-4

2,4-di-tert-Butylphenol

2-ethyl-5-methypyrazine
13360-64-0

2-ethyl-5-methypyrazine

3-ethyl-2-hydroxy-2-cyclopenten-1-one
21835-01-8

3-ethyl-2-hydroxy-2-cyclopenten-1-one

Conditions
Conditions Yield
With sodium hydroxide; at 143 ℃; for 2h; pH=5; aq. phosphate buffer; Sealed vial;
L-serin
56-45-1,83245-15-2

L-serin

ascorbic acid
50-81-7,98966-42-8

ascorbic acid

2-Methylpyrazine
109-08-0

2-Methylpyrazine

2,5-dimethyl-pyrazine
123-32-0

2,5-dimethyl-pyrazine

1-benzofurane
271-89-6

1-benzofurane

2-ethylpyrazine
13925-00-3

2-ethylpyrazine

2,5-diformylfurane
823-82-5,163857-09-8

2,5-diformylfurane

2-ethyl-3,6-dimethylpyrazine
13360-65-1

2-ethyl-3,6-dimethylpyrazine

1-furfuryl-pyrrole
1438-94-4

1-furfuryl-pyrrole

2,4-di-tert-Butylphenol
96-76-4

2,4-di-tert-Butylphenol

2-ethyl-5-methypyrazine
13360-64-0

2-ethyl-5-methypyrazine

3-ethyl-2-hydroxy-2-cyclopenten-1-one
21835-01-8

3-ethyl-2-hydroxy-2-cyclopenten-1-one

Conditions
Conditions Yield
With sodium hydroxide; at 143 ℃; for 2h; pH=6; aq. phosphate buffer; Sealed vial;

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