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2-Ethyl-3-methylpyrazine is an organic compound with a strong, raw-potato, roasted, and earthy odor. It is a clear colorless to slightly yellow liquid and is known for its distinct taste characteristics, which include nutty, peanut, and musty corn-like flavors with raw and oily nuances. 2-Ethyl-3-methylpyrazine is commonly found in a variety of food products, such as bakery items, roasted barley, coffee, peanuts, filberts, potato products, soy products, roasted and fried chicken, beef, pork, beer, rum, cocoa, coffee, tea, malt, and seafood like shrimp and crayfish.

15707-23-0

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15707-23-0 Usage

Uses

1. Used in the Flavor and Fragrance Industry:
2-Ethyl-3-methylpyrazine is used as a flavoring agent for its nutty, peanut, and musty corn-like taste characteristics. It is particularly useful in enhancing the flavor of various food products, such as bakery items, roasted barley, coffee, peanuts, filberts, potato products, and soy products.
2. Used in the Food Additive Industry:
As a food additive, 2-Ethyl-3-methylpyrazine is employed to impart a unique taste and aroma to a wide range of products, including roasted and fried chicken, beef, pork, beer, rum, cocoa, coffee, tea, and malt.
3. Used in the E-cigarette Industry:
2-Ethyl-3-methylpyrazine is used in the preparation of Chinese chestnut pyrolyzate, which is then applied to e-cigarettes. Its strong, raw-potato, roasted, and earthy odor contributes to the overall flavor and sensory experience of e-cigarette vapor.
4. Used in the Aroma Compound Research:
Due to its distinct odor and taste characteristics, 2-Ethyl-3-methylpyrazine is also utilized in the research and development of new aroma compounds for various applications, such as perfumery and the creation of artificial flavors.

Preparation

By condensation of ethylenediamine with 2,3-pentanedione.

Hazard

Moderately toxic by ingestion.

Flammability and Explosibility

Notclassified

Safety Profile

Moderately toxic by ingestion. When heated to decomposition it emits acrid smoke and irritating fumes.

Check Digit Verification of cas no

The CAS Registry Mumber 15707-23-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,7,0 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 15707-23:
(7*1)+(6*5)+(5*7)+(4*0)+(3*7)+(2*2)+(1*3)=100
100 % 10 = 0
So 15707-23-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H10N2/c1-3-7-6(2)8-4-5-9-7/h4-5H,3H2,1-2H3

15707-23-0 Well-known Company Product Price

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  • Alfa Aesar

  • (A11092)  2-Ethyl-3-methylpyrazine, 98+%   

  • 15707-23-0

  • 5g

  • 362.0CNY

  • Detail
  • Alfa Aesar

  • (A11092)  2-Ethyl-3-methylpyrazine, 98+%   

  • 15707-23-0

  • 25g

  • 1383.0CNY

  • Detail
  • Alfa Aesar

  • (A11092)  2-Ethyl-3-methylpyrazine, 98+%   

  • 15707-23-0

  • 100g

  • 4430.0CNY

  • Detail

15707-23-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Ethyl-3-methylpyrazine

1.2 Other means of identification

Product number -
Other names FEMA 3155

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:15707-23-0 SDS

15707-23-0Related news

Syntheses, structures, thermal stabilities and photoluminescent properties of three silver(I) complexes of 2-Ethyl-3-methylpyrazine (cas 15707-23-0) and different aromatic dicarboxylates with various silver units09/03/2019

Three new silver(I) coordination compounds based on 2-ethyl-3-methylpyrazine (epyz), [Ag2(epyz)(pta] (1), [Ag4(epyz)2(ipa)2] (2) and [Ag8(epyz)4(npa)4] (3, H2pta = o-phthalic acid, H2ipa = m-phthalic acid, H2npa = 1,4-napthalenedicarboxylic acid), have been synthesized and have been characterize...detailed

15707-23-0Relevant articles and documents

Efficient synthesis method of 2-ethyl-3-methylpyrazine

-

Paragraph 0024; 0029; 0035; 0041; 0049; 0053, (2018/04/01)

The invention discloses an efficient synthesis method of 2-ethyl-3-methylpyrazine. The method comprises specific steps as follows: 2,3-pentanedione is prepared from lactic acid as a raw material, a porous carrier is prepared from raw materials including diammonium hydrogen phosphate and barium nitrate, caesium supported on the carrier is taken as a catalyst, and the conversion rate of lactic acidis effectively increased; then, prepared 2,3-pentanedione and ethylenediamine are taken as raw materials and are sequentially subjected to dehydration condensation and dehydrogenation reactions, and 2-ethyl-3-methylpyrazine is prepared. The synthesis method is simple, low in cost and high in product yield.

Influence of Free Amino Acids, Oligopeptides, and Polypeptides on the Formation of Pyrazines in Maillard Model Systems

Scalone, Gustavo Luis Leonardo,Cucu, Tatiana,De Kimpe, Norbert,De Meulenaer, Bruno

, p. 5364 - 5372 (2015/06/25)

Pyrazines are specific Maillard reaction compounds known to contribute to the unique aroma of many products. Most studies concerning the generation of pyrazines in the Maillard reaction have focused on amino acids, while little information is available on the impact of peptides and proteins. The present study investigated the generation of pyrazines in model systems containing whey protein, hydrolyzed whey protein, amino acids, and glucose. The impact of thermal conditions, ratio of reagents, and water activity (aw) on pyrazine formation was measured by headspace solid-phase microextraction with gas chromatography/mass spectrometry (HS-SPME-GC/MS. The presence of oligopeptides from hydrolyzed whey protein contributed significantly to an increased amount of pyrazines, while in contrast free amino acids generated during protein hydrolysis contributed to a lesser extent. The generation of pyrazines was enhanced at low aw (0.33) and high temperatures (>120 °C). This study showed that the role of peptides in the generation of pyrazines in Maillard reaction systems has been dramatically underestimated.

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, formed from the reactions of l-ascorbic acid with l-threonine/l-serine at five different pH values (5.00, 6.00, 7.00, 8.00, or 9.55) and 143 ± 2 °C for 2 h, was performed using a SPME-GC-MS technique, and further use

Pt/Al2O3 CATALYSTS IN THE SYNTHESIS OF NITROGEN HETEROCYCLES. CATALYTIC SYNTHESIS OF PYRAZINES

Gitis, K. M.,Neumoeva, G. E.,Isagulyants, G. V.

, p. 1308 - 1315 (2007/10/02)

A study was carried out on the use of Pt/Al2O3 catalysts in the synthesis of pyrazines via the dehydrogenation of piperazines, dehydrodeamination of diamines, and dehydrocyclocondensation of N-hydroxyalkyldiamines.In contrast to the current hypothesis of the intermediate formation of piperazine in the latter two reactions, evidence was found that these reactions proceed through initial dehydrogenation and the dehydrogenated intermediate then undergoes cyclization.Polyalkylpyrazines, formed by the alkylation of the pyrazine ring by hydrogenolysis products, are the major side-products in all the reactions studied.Pyrazines may be obtained in high yield and satisfactory selectivity by selecting suitable modifiers, which enhance the dehydrogenation activity of the catalyst and suppress the hydrogenolysis of the C-N bond.

Ueber die Synthese von 2,3-Dialkylpyrazinen

Heyns, Kurt,Behse, Ernst,Francke, Wittko

, p. 240 - 245 (2007/10/02)

2,3-Dialkylquinoxalines (4), which are available from the reaction of benzofuroxan (1) with ketones and subsequent reduction of the 2,3-dialkylquinoxaline N,N'-dioxides (3), are converted to 2,3-dialkylpyrazines (6) by oxidation-decarboxylation steps.

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