Skip to Content
Merck
All Photos(1)

Key Documents

8.09691

Sigma-Aldrich

m-Cresol

for synthesis

Synonym(s):

m-Cresol, 3-Hydroxytoluol, 3-Methylphenol

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
3-(CH3)C6H4OH
CAS Number:
Molecular Weight:
108.14
MDL number:
UNSPSC Code:
12352104
EC Index Number:
203-577-9
NACRES:
NA.22

vapor pressure

0.065 hPa ( 20 °C)

Quality Level

Assay

≥99.0% (GC)

form

liquid

autoignition temp.

626 °C

potency

242 mg/kg LD50, oral (Rat)

expl. lim.

1.06 % (v/v)

pH

5 (20 °C, 20 g/L in H2O)

bp

203 °C/1013 hPa

mp

11.5 °C

transition temp

flash point 86 °C

solubility

23.5 g/L

density

1.03 g/cm3 at 20 °C

storage temp.

2-30°C

InChI

1S/C7H8O/c1-6-3-2-4-7(8)5-6/h2-5,8H,1H3

InChI key

RLSSMJSEOOYNOY-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

m-Cresol can be used as a starting material to synthesize:
  • Thymol via isopropylation reaction with 2-propanol in the presence of an acid catalyst.
  • Terpolymeric resin by an acid-catalyzed polycondensation reaction with hexamine and formaldehyde.
  • 4,7-Dimethylcoumarin via modified Pechmann condensation reaction with ethyl acetoacetate.

Analysis Note

Assay (GC, area%): ≥ 99.0 % (a/a)
Density (d 20 °C/ 4 °C): 1.031 - 1.037
Identity (IR): passes test
Due to its specific melting range the product may be solid, liquid, a solidified melt or a supercooled melt.
Appearance: colorless to dark yellow/light brown. Material may darken with time.

Pictograms

Skull and crossbonesCorrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 2

Flash Point(F)

186.8 °F - closed cup

Flash Point(C)

86 °C - closed cup


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’.

Already Own This Product?

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

Visit the Document Library

Synthesis, Chacterization, and Thermal Study of Terpolymeric Resin Derived from m-cresol, Hexamine and Formaldehyde
Khedkar KM, et al.
E-Journal of Chemistry, 9(4), 1911-1918 (2012)
Ganapati D Yadav et al.
The journal of physical chemistry. A, 109(48), 11080-11088 (2005-12-08)
The alkylation of m-cresol with isopropyl alcohol in the presence of novel superacidic catalysts named as UDCaT-4, UDCaT-5, and UDCaT-6 was investigated. The catalysts are modified versions of zirconia showing high catalytic activity, stability, and reusability in the presence of
Comparison of mesoporous and microporous solid acid catalysts for highly selective synthesis of thymol by vapor phase isopropylation of m-cresol
Selvaraj M and Kawi S
Microporous and Mesoporous Materials : The Official Journal of the International Zeolite Association, 109(1-3), 458-469 (2008)
Synthesis and antioxidant activity of selected 4-methylcoumarins
Cavar S, et al.
Food Chemistry, 117(1), 135-142 (2009)

Protocols

Fmoc resin cleavage and deprotection are crucial steps for peptide synthesis, yielding the desired peptide after resin detachment.

Fmoc resin cleavage and deprotection are crucial steps for peptide synthesis, yielding the desired peptide after resin detachment.

Fmoc resin cleavage and deprotection are crucial steps for peptide synthesis, yielding the desired peptide after resin detachment.

Fmoc resin cleavage and deprotection are crucial steps for peptide synthesis, yielding the desired peptide after resin detachment.

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