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Merck
CN

W327204

Sigma-Aldrich

2,5-二甲基吡嗪

≥98%, FG

别名:

Ketine

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关于此项目

经验公式(希尔记法):
C6H8N2
CAS Number:
分子量:
108.14
FEMA编号:
3272
Beilstein:
107052
EC 号:
欧洲委员会编号:
2210
MDL编号:
UNSPSC代码:
12164502
PubChem化学物质编号:
Flavis编号:
14.020
NACRES:
NA.21
Agency:
follows IFRA guidelines
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生物来源

synthetic

质量水平

等级

FG
Fragrance grade
Halal
Kosher

Agency

follows IFRA guidelines

管理合规性

EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002

方案

≥98%

折射率

n20/D 1.502 (lit.)

沸点

155 °C (lit.)

密度

0.99 g/mL at 25 °C (lit.)

应用

flavors and fragrances

文件

see Safety & Documentation for available documents

食品过敏原

no known allergens

致敏芳香化合物

no known allergens

性状检查

cocoa; nutty; woody; earthy

SMILES字符串

Cc1cnc(C)cn1

InChI

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

InChI key

LCZUOKDVTBMCMX-UHFFFAOYSA-N

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一般描述

2,5-二甲基吡嗪是一种吡嗪类化合物,主要在烹煮或烘烤过程中,由于糖类和蛋白质之间的美拉德反应,在熟米或烘烤花生等食品中形成。

应用


  • 通过重建代谢途径和增强辅因子再生,工程化大肠杆菌由L-苏氨酸高产合成2,5-二甲基吡嗪。:研究详细介绍了*大肠杆菌*的基因工程,可提高由L-苏氨酸生成2,5-二甲基吡嗪的效率。通过重建代谢途径和改善辅因子再生,研究人员实现了更高的产量,这是该化合物工业生物生产的重大进展(Liu et al., 2024)。

  • 从纳豆发酵大豆中分离的芽孢杆菌菌株生物合成吡嗪的研究。:研究探讨了从纳豆中分离的*芽孢杆菌*菌株对2,5-二甲基吡嗪等吡嗪类化合物的天然生物合成。这些发现有助于了解风味化合物的微生物生产及其在食品生物技术中的潜在应用(Klosowski et al., 2021)。

其他说明

残留物 2,6-二甲基吡嗪

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

147.2 °F - closed cup

闪点(°C)

64 °C - closed cup

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Flavor components of roasted peanuts. Some low molecular weight pyrazines and pyrrole.
Mason ME, et al.
Journal of Agricultural and Food Chemistry, 14(5), 454-460 (1966)
W Ma et al.
Biology of reproduction, 59(6), 1317-1320 (1998-11-26)
Mature female mice, grouped in the absence of a male stimulus, exhibit a suppressed estrous cycle (the so-called Lee-Boot effect). We have designed a series of experiments to elucidate the involvement of the adrenal gland in this phenomenon. Our initial
Roger N Thompson et al.
Chemical senses, 31(7), 613-619 (2006-06-08)
The social and reproductive behaviors of most mammals are modulated by pheromones, which are perceived by the vomeronasal organ (VNO). Vomeronasal transduction in vertebrates is activated through G-protein-coupled receptors, which in turn leads to the generation of inositol 1,4,5-trisphosphate (IP(3))
Katharina Mamasuew et al.
Chemical senses, 36(3), 271-282 (2010-12-15)
Based on a variety of recent findings, the Grueneberg ganglion (GG) in the vestibule of the nasal cavity is considered as an olfactory compartment. However, defined chemical substances that activate GG neurons have not been identified. In this study, the
Roger N Thompson et al.
Chemical senses, 29(9), 749-754 (2004-12-03)
Social behaviors of most mammals are affected by chemical signals, pheromones, exchanged between conspecifics. Previous experiments have shown that behavioral responses to the same pheromone differ depending on the sex and endocrine status of the respondent. Although the exact mechanism

实验方案

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

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