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W320404

Sigma-Aldrich

4-甲基-5-噻唑乙醇

≥98%, FG

别名:

5-(2-羟乙基)-4-甲基噻唑, 磺酰醇

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About This Item

经验公式（希尔记法）:
C6H9NOS
CAS号:
137-00-8
分子量:
143.21
FEMA號碼:
3204
Beilstein:
114249
EC號碼:
205-272-6
歐洲委員會號碼:
11621
MDL號碼:
MFCD00005339
分類程式碼代碼:
12164502
PubChem物質ID:
24901552
Flavis號碼:
15.014
NACRES:
NA.21
agency:
follows IFRA guidelines
meets purity specifications of JECFA

生物源

synthetic

品質等級

400

等級

FG
Fragrance grade
Halal
Kosher

agency

follows IFRA guidelines
meets purity specifications of JECFA

法律遵循

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

化驗

≥98%

折射率

n20/D 1.550 (lit.)

bp

135 °C/7 mmHg (lit.)

密度

1.196 g/mL at 25 °C (lit.)

應用

flavors and fragrances

文件

see Safety & Documentation for available documents

食物過敏原

no known allergens

香料過敏原

no known allergens

感官的

fatty; meaty; nutty

儲存溫度

room temp

SMILES 字串

Cc1ncsc1CCO

InChI

1S/C6H9NOS/c1-5-6(2-3-8)9-4-7-5/h4,8H,2-3H2,1H3

InChI 密鑰

BKAWJIRCKVUVED-UHFFFAOYSA-N

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相关类别

一般說明

4-甲基-5-噻唑乙醇是一种含硫杂环风味化合物，据报道其产生于考姆特芝士和人参中。

應用


  • New aspects characterizing non-obese NAFLD by the analysis of the intestinal flora and metabolites using a mouse model.：研究非肥胖型非酒精性脂肪性肝病(NAFLD)影响的代谢途径，其中4-甲基-5-噻唑乙醇有调节肠道微生物群落的作用，可作为治疗标志物(Zhang et al., 2024)。

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險聲明

H315,H319,H335

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

10 - Combustible liquids

水污染物質分類（WGK）

WGK 2

閃點（°F）

233.6 °F - closed cup

閃點（°C）

112 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
SHBN6262
SHBM1450
STBG8108
MKCJ2603
MKCJ2602

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Flavor constituents of aqueous fraction extracted from Comte cheese by liquid carbon dioxide.
Roudot?Algaron F, et al.
Journal of Food Science, 58(5), 1005-1009 (1993)
A thiazole and two β-carboline constitutents from Panax ginseng.
Park JD, et al.
Archives of Pharmacal Research, 11(1), 52-55 (1988)
C Niederberger et al.
Gene, 171(1), 119-122 (1996-05-24)
Amiloride (Am) inhibits growth in the fission yeast Schizosaccharomyces pombe. We show that the toxic effect of this drug is relieved by low concentrations of thiamine (Th) and that the pyrimidine moiety of the Th molecule is responsible for growth
Biosynthesis of thiamin thiazole: determination of the regiochemistry of the S/O acyl shift by using 1,4-dideoxy-D-xylulose-5-phosphate.
Abhishek Chatterjee et al.
Angewandte Chemie (International ed. in English), 45(21), 3507-3510 (2006-04-21)
S A Petrov et al.
Ukrainskii biokhimicheskii zhurnal (1978), 59(3), 76-79 (1987-05-01)
Thiamine, thiaminepyrophosphate and 4-methyl-5-beta-oxyethylthiazole are studied for their effect on the acetylcholinesterase activity in the brain, blood plasma and cells. The activity of acetylcholinesterase in blood cells is shown to be inhibited most of all by thiamine and thiazole. Acetylcholinesterase
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