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18138-05-1

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18138-05-1 Usage

Chemical Properties

3,5-Diethyl-2-methylpyrazine has a nutty, meaty, vegetable odor

Occurrence

Reported found in potato, chicken, beef, pork (0.1 to 0.5 ppm), cocoa (2.1 ppm), coffee, tea, peanut, coconut (1 ppm), corn, shrimp (0.002 ppm).

Check Digit Verification of cas no

The CAS Registry Mumber 18138-05-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,3 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18138-05:
(7*1)+(6*8)+(5*1)+(4*3)+(3*8)+(2*0)+(1*5)=101
101 % 10 = 1
So 18138-05-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H14N2/c1-4-8-6-10-7(3)9(5-2)11-8/h6H,4-5H2,1-3H3

18138-05-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-diethyl-3-methylpyrazine

1.2 Other means of identification

Product number -
Other names 3,5-DIETHYL-2-METHYL PYRAZINE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
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:18138-05-1 SDS

18138-05-1Downstream Products

18138-05-1Relevant articles and documents

Flavor components of roasted almond

Takei,Yamanishi

, p. 2329 - 2336 (1974)

-

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

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