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W323713

Sigma-Aldrich

2,3,5,6-四甲基吡嗪

greener alternative

natural, ≥98%, FG

别名:

四甲基吡嗪碱, 川芎嗪

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About This Item

经验公式（希尔记法）:
C8H12N2
CAS号:
1124-11-4
分子量:
136.19
FEMA编号:
3237
Beilstein:
113100
EC 号:
214-391-2
MDL编号:
MFCD00006146
UNSPSC代码:
12164502
PubChem化学物质编号:
24901576
Flavis编号:
14.018
NACRES:
NA.21
性状检查:
chocolate; coffee; fatty; musty; nutty
等级:
FG
Fragrance grade
Halal
Kosher
natural
Agency:
follows IFRA guidelines
meets purity specifications of JECFA
食品过敏原:
no known allergens

等级

FG
Fragrance grade
Halal
Kosher
natural

质量水平

400

Agency

follows IFRA guidelines
meets purity specifications of JECFA

管理合规性

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

方案

≥98%

环保替代产品特性

Less Hazardous Chemical Syntheses
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

杂质

≤2.0% water (Karl Fischer)

沸点

190 °C (lit.)

mp

77-80 °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

环保替代产品分类

, Aligned

性状检查

chocolate; coffee; fatty; musty; nutty

SMILES字符串

Cc1nc(C)c(C)nc1C

InChI

1S/C8H12N2/c1-5-6(2)10-8(4)7(3)9-5/h1-4H3

InChI key

FINHMKGKINIASC-UHFFFAOYSA-N

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相关类别

一般描述

2，3，5，6-四甲基吡嗪是烤可可豆和枫糖浆中的主要挥发性香气化合物之一。
我们竭诚为您带来满足绿色替代产品四大类别要求的替代产品。本品为生物基产品，在“危险性较小的化学合成”和“使用可再生原料”绿色化学原则方面取得了重大进步。

应用


  • 2,3,5,6-四甲基吡嗪和紫外光的结合能有效地吸引嗜脂虫。：该研究表明，2,3,5,6-四甲基吡嗪和紫外线的组合有效地吸引了书虫，这表明在储存产品环境中害虫管理的潜在应用（Tanaka et al., 2024）。

  • 2,3,5,6-四甲基吡嗪通过调节ATF4介导的PRP聚集抑制来保护视网膜光感受器免受内质网应激。：该研究强调了2,3,5,6-四甲基吡嗪的神经保护作用，显示其通过保护光感受器免受应激性损伤来治疗视网膜疾病的潜力（Huang et al., 2021）。

  • 约氏红球菌的TMP1四甲基吡嗪诱导启动子区。：该研究在约氏红球菌TMP1中发现了一个由四甲基吡嗪诱导的启动子区域，可用于基因工程和生物技术应用（Stanislauskienė et al., 2018）。

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险分类

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
SHBR6644
SHBS0294
SHBQ8589
SHBN2561
SHBM9557

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Quantitation of alkylpyrazines in maple syrup, maple flavors and non-maple syrups.
Akochi-KE, et al.
Food Research International, 27(5), 451-457 (1994)
Donghui Xu et al.
Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology, 49(5), 2012-2021 (2018-09-24)
Ligustrazine (LSZ) has been identified as an antitumor agent against some types of cancers. Nevertheless, its ability to inhibit growth, migration and invasion of medulloblastoma cells is still unclear. This study aimed to explore the effect of LSZ on Daoy
Xian-Chao Cheng et al.
Bioorganic & medicinal chemistry, 17(8), 3018-3024 (2009-03-31)
A series of novel acylpiperazinyl Ligustrazine derivatives was designed, synthesized, and their protective effects on damaged ECV-304 cells and antiplatelet aggregation activities were evaluated. The results showed that compound E33 displayed most potential protective effects on the ECV-304 cells damaged
Xian-Chao Cheng et al.
Bioorganic & medicinal chemistry, 15(10), 3315-3320 (2007-03-27)
A series of novel Ligustrazine derivatives was designed, synthesized, and assayed for their protective effects on damaged ECV-304 cells and antiplatelet aggregation activities. The results showed that most Ligustrazine derivatives exhibited lower EC(50) values for protective effects on the ECV-304
Hongfei Chen et al.
European journal of medicinal chemistry, 46(11), 5609-5615 (2011-10-14)
A series of novel ligustrazinyloxy-cinnamic acid derivatives were designed, synthesized and evaluated for their inhibitory effect on adenosine diphosphate (ADP)-induced platelet aggregation in vitro, and also assayed for their protective effect against hydrogen peroxide (H(2)O(2))-induced oxidative damage on ECV-304 cells.
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