Skip to Content
Merck
CN

W515507

2,5-Dimethylthiophene

≥98%

Synonym(s):

NSC 60689

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Empirical Formula (Hill Notation):
C6H8S
CAS Number:
Molecular Weight:
112.19
NACRES:
NA.21
Flavis number:
15.064
PubChem Substance ID:
UNSPSC Code:
12164502
EC Number:
211-313-9
MDL number:
Beilstein/REAXYS Number:
106450
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

2,5-Dimethylthiophene, ≥98%

InChI key

GWQOOADXMVQEFT-UHFFFAOYSA-N

InChI

1S/C6H8S/c1-5-3-4-6(2)7-5/h3-4H,1-2H3

SMILES string

Cc1ccc(C)s1

biological source

synthetic

grade

Halal
Kosher

assay

≥98%

refractive index

n20/D 1.512 (lit.)

bp

134 °C/740 mmHg (lit.)

density

0.985 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

organoleptic

sulfurous

Looking for similar products? Visit Product Comparison Guide

General description

2,5-Dimethylthiophene is a volatile flavoring compound that has been identified in the essential oil of onion. It is reported to be one of the sulfur-containing compounds formed via Maillard reaction/Strecker degradation of cysteine with furaneol.

pictograms

Flame

signalword

Warning

hcodes

Hazard Classifications

Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

75.2 °F - closed cup

flash_point_c

24 °C - closed cup

ppe

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

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Formation of sulfur-containing flavor compounds from reactions of furaneol and cysteine, glutathione, hydrogen sulfide, and alanine/hydrogen sulfide.
Zheng Y, et al.
Journal of Agricultural and Food Chemistry, 45(3), 894-897 (1997)
Volatile flavor compounds from onion.
Boelens M, et al.
Journal of Agricultural and Food Chemistry, 19(5), 984-991 (1971)
Restituto Tocmo et al.
Journal of agricultural and food chemistry, 62(23), 5296-5304 (2014-05-21)
There is a growing account of the health benefits of H2S as an endogenous cell-signaling molecule. H2S from organic polysulfides, in particular, is increasingly gaining attention for their beneficial effects to cardiovascular health. Here, we studied shallot as a potential

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service