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2-N-Butyl-3-Methylpyrazine is an organic compound with the molecular formula C9H14N2. It is a colorless to pale yellow liquid with a strong, earthy, and nutty odor. 2-N-BUTYL-3-METHYLPYRAZINE is commonly found in the chemical composition of various natural products, particularly in the realm of food and beverages, where it contributes to the overall aroma and flavor profile.

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  • 15987-00-5 Structure
  • Basic information

    1. Product Name: 2-N-BUTYL-3-METHYLPYRAZINE
    2. Synonyms: 2-N-BUTYL-3-METHYLPYRAZINE;2-BUTYL-3-METHYLPYRAZINE;BUTYL-3-METHYLPYRAZINE, 2-;2-butyl-3-methyl-pyrazin;2-methyl-3- butylpyrazine;Pyrazine, 2-butyl-3-methyl-;Butylmethylpyrazine;BUTYL-3-METHYLPYRAZINE,2-(SG)
    3. CAS NO:15987-00-5
    4. Molecular Formula: C9H14N2
    5. Molecular Weight: 150.22
    6. EINECS: 240-126-5
    7. Product Categories: Mono- & Polyalkylpyrazines;Pyrazines
    8. Mol File: 15987-00-5.mol
    9. Article Data: 3
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 84 °C / 9mmHg
    3. Flash Point: 83℃
    4. Appearance: /
    5. Density: 0.95
    6. Vapor Pressure: 0.217mmHg at 25°C
    7. Refractive Index: 1.4920 to 1.4960
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. PKA: 1.93±0.10(Predicted)
    11. CAS DataBase Reference: 2-N-BUTYL-3-METHYLPYRAZINE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 2-N-BUTYL-3-METHYLPYRAZINE(15987-00-5)
    13. EPA Substance Registry System: 2-N-BUTYL-3-METHYLPYRAZINE(15987-00-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 15987-00-5(Hazardous Substances Data)

15987-00-5 Usage

Uses

Used in Flavor and Fragrance Industry:
2-N-Butyl-3-Methylpyrazine is used as an aroma component for its characteristic earthy and nutty scent. It is particularly valued in the flavor and fragrance industry for its ability to enhance the aroma of roasted cocoa beans, which are a key ingredient in the production of chocolate.
Used in the Synthesis of Aqueous Formulations:
2-N-Butyl-3-Methylpyrazine is also utilized in the synthesis of aqueous formulations that are rich in pyrazines. These formulations find applications in various industries, including the food and beverage sector, where they can be used to create complex and nuanced flavor profiles. The compound's unique properties make it a valuable addition to the development of new and innovative products in this field.

Check Digit Verification of cas no

The CAS Registry Mumber 15987-00-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,8 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 15987-00:
(7*1)+(6*5)+(5*9)+(4*8)+(3*7)+(2*0)+(1*0)=135
135 % 10 = 5
So 15987-00-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H14N2/c1-3-4-5-9-8(2)10-6-7-11-9/h6-7H,3-5H2,1-2H3

15987-00-5SDS

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-Butyl-3-methylpyrazine

1.2 Other means of identification

Product number -
Other names 2-N-BUTYL-3-METHYLPYRAZINE

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:15987-00-5 SDS

15987-00-5Downstream Products

15987-00-5Relevant articles and documents

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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