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269689

Sigma-Aldrich

3,4-Dimethylbenzenethiol

98%

Synonym(s):

3,4-Dimethylthiophenol

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About This Item

Linear Formula:
(CH3)2C6H3SH
CAS Number:
18800-53-8
Molecular Weight:
138.23
EC Number:
242-587-8
MDL number:
MFCD00010023
UNSPSC Code:
12352100
PubChem Substance ID:
24856339
NACRES:
NA.22

Quality Level

100

Assay

98%

refractive index

n20/D 1.5736 (lit.)

bp

218 °C (lit.)

density

1.027 g/mL at 25 °C (lit.)

SMILES string

Cc1ccc(S)cc1C

InChI

1S/C8H10S/c1-6-3-4-8(9)5-7(6)2/h3-5,9H,1-2H3

InChI key

IDKCKPBAFOIONK-UHFFFAOYSA-N

Application

3,4-Dimethylbenzenethiol may be used in chemical synthesis studies.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

194.0 °F - closed cup

Flash Point(C)

90 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Francesca Bettazzi et al.
Food chemistry, 344, 128692-128692 (2020-12-23)
An easy and reliable method based on a novel electroanalytical nanostructured sensor has been developed to perform quantification of vitamin C in commercial and fortified cow-milk-based formulae and foods for infants and young children. The work is motivated by the
Maria Principia Scavo et al.
Cells, 8(8) (2019-07-28)
Extracellular vesicles (EVs) are involved in intercellular communication during carcinogenesis, and cancer cells are able to secrete EVs, in particular exosomes containing molecules, that can be transferred to recipient cells to induce pathological processes and significant modifications, as metastasis, increase
Homan Kang et al.
Scientific reports, 5, 10144-10144 (2015-05-29)
Recently, preparation and screening of compound libraries remain one of the most challenging tasks in drug discovery, biomarker detection, and biomolecular profiling processes. So far, several distinct encoding/decoding methods such as chemical encoding, graphical encoding, and optical encoding have been

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