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250384

Sigma-Aldrich

Ethylpyrazine

98%

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About This Item

Empirical Formula (Hill Notation):
C6H8N2
CAS Number:
Molecular Weight:
108.14
Beilstein:
108200
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

refractive index

n20/D 1.498 (lit.)

bp

152-153 °C (lit.)

density

0.984 g/mL at 25 °C (lit.)

SMILES string

CCc1cnccn1

InChI

1S/C6H8N2/c1-2-6-5-7-3-4-8-6/h3-5H,2H2,1H3

InChI key

KVFIJIWMDBAGDP-UHFFFAOYSA-N

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Application

Ethylpyrazine has been used in the synthesis of pyrazinoic acid.

Pictograms

FlameExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

109.0 °F

Flash Point(C)

42.78 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Notes. Synthesis of Pyrazinoic Acid.
Gainer H.
The Journal of Organic Chemistry, 24(5), 691-691 (1959)
Gustavo Luis Leonardo Scalone et al.
Journal of agricultural and food chemistry, 63(22), 5364-5372 (2015-05-15)
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

Protocols

Separation of various pyrazines and sulfur compounds including carbon disulfide and dimethyl disulfide.

Separation of various pyrazines and sulfur compounds including carbon disulfide and dimethyl disulfide.

Separation of various pyrazines and sulfur compounds including carbon disulfide and dimethyl disulfide.

Separation of various pyrazines and sulfur compounds including carbon disulfide and dimethyl disulfide.

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