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Merck
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Documenti fondamentali

W318809

Sigma-Aldrich

2-Methyl-3-furanthiol

≥95%, FG

Sinonimo/i:

2-methyl-3-furyl mercaptan, Fish thiol, Oxy cyclothione-030

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About This Item

Formula empirica (notazione di Hill):
C5H6OS
Numero CAS:
Peso molecolare:
114.17
Numero FEMA:
3188
Numero CE:
N° CoE:
11678
Numero MDL:
Codice UNSPSC:
12164502
ID PubChem:
Numero Flavis:
13.055
NACRES:
NA.21
Organolettico:
fishy; meaty; metallic; sulfurous
Grado:
FG
Fragrance grade
Halal
Kosher
Origine biologica:
synthetic
agenzia:
follows IFRA guidelines
Allergene alimentare:
no known allergens

Origine biologica

synthetic

Livello qualitativo

Grado

FG
Fragrance grade
Halal
Kosher

agenzia

follows IFRA guidelines

Conformità normativa

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

Densità del vapore

>1 (vs air)

Saggio

≥95%

Indice di rifrazione

n20/D 1.518 (lit.)

P. ebollizione

57-60 °C/44 mmHg (lit.)

Densità

1.145 g/mL at 25 °C

applicazioni

flavors and fragrances

Documentazione

see Safety & Documentation for available documents

Allergene alimentare

no known allergens

Allergene in fragranze

no known allergens

Organolettico

fishy; meaty; metallic; sulfurous

Stringa SMILE

Cc1occc1S

InChI

1S/C5H6OS/c1-4-5(7)2-3-6-4/h2-3,7H,1H3
RUYNUXHHUVUINQ-UHFFFAOYSA-N

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Descrizione generale

2-Methyl-3-furanthiol, a sulfur-containing compound, is the key odorant in cooked ham, wine and canned tuna fish.

Applicazioni


  • Elucidating salt-reduction mechanisms of aroma-active compounds from yeast extracts through sensomics approaches and electroencephalography.: This innovative study leverages both sensory science and neurotechnology to uncover how 2-methyl-3-furanthiol and other key compounds in yeast extracts can enhance flavor profiles while reducing sodium content in foods, aligning with health trends and consumer demands for lower-sodium options (Shan et al., 2024).

  • Widely Targeted Metabolomics and Network Pharmacology Reveal the Nutritional Potential of Yellowhorn (Xanthoceras sorbifolium Bunge) Leaves and Flowers.: This study demonstrates the use of targeted metabolomics to profile bioactive compounds, including 2-methyl-3-furanthiol, in Yellowhorn plant parts, which are emerging as a nutritional powerhouse with potential health benefits (Sha et al., 2024).

  • Metabolomics reveals factors affecting the radical reaction of sulfides during thermal processing for meaty aroma.: This research identifies how 2-methyl-3-furanthiol and other sulfides interact during cooking to create rich, meaty flavors, providing valuable insights for the culinary industry on optimizing flavor profiles in cooked meats (Zhang et al., 2024).

Azioni biochim/fisiol

Taste at 10 ppm

Pittogrammi

FlameSkull and crossbones

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Acute Tox. 3 Oral - Flam. Liq. 3

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

98.6 °F - closed cup

Punto d’infiammabilità (°C)

37 °C - closed cup

Dispositivi di protezione individuale

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


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I clienti hanno visto anche

A novel method for quantification of 2-methyl-3-furanthiol and 2-furanmethanethiol in wines made from Vitis vinifera grape varieties.
Tominaga T & Dubourdieu D
Journal of Agricultural and Food Chemistry, 54(1), 29-33 (2006)
Caroline Thomas et al.
Food chemistry, 155, 207-213 (2014-03-07)
The aim of this work was to identify and gain further knowledge on the origin of sulfur compounds present in the volatile fraction of cooked ham, and on their role in the aroma of this product. To this end, we
Mosciano, G.
Perfumer & Flavorist, 26, 58-58 (2001)
Identification of 2-Methyl-3-Furanthiol in the Steam Distillate from Canned Tuna Fish.
WITHYCOMBE D and MUSSINAN CYJ.
Journal of Food Science, 53(2), 658-658 (1988)
Mosciano, G.
Perfumer & Flavorist, 21, 53-53 (1996)

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