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Key Documents

65996

Supelco

m-Cresol

analytical standard

Synonym(s):

1-Hydroxy-3-methylbenzene, 3-Hydroxytoluene, 3-Methylphenol

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About This Item

Linear Formula:
CH3C6H4OH
CAS Number:
Molecular Weight:
108.14
Beilstein:
506719
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

vapor density

3.72 (vs air)

vapor pressure

<1 mmHg ( 20 °C)

Assay

≥99.0% (GC)

autoignition temp.

1036 °F

shelf life

limited shelf life, expiry date on the label

expl. lim.

1.06-1.35 %, 150 °F

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.541 (lit.)
n20/D 1.542

bp

203 °C (lit.)

mp

8-10 °C (lit.)

density

1.034 g/mL at 25 °C (lit.)

application(s)

agriculture
cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care

format

neat

SMILES string

Cc1cccc(O)c1

InChI

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

InChI key

RLSSMJSEOOYNOY-UHFFFAOYSA-N

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General description

This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food.

Find all available reference materials for compounds listed in 10/2011 here
m-Cresol is an isomer form of Cresol and is mainly used as an intermediate in the manufacture of chemicals. It is toxic in nature.

Application

It was used as reference standard solution for determination of phenolic compounds in tyrosinase biosensor using amperometric detection under self-assembled monolayers-based bioelectrode flow-injection.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number

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Customers Also Viewed

Amperometric flow-injection determination of phenolic compounds at self-assembled monolayer-based tyrosinase biosensors.
Campuzano, Susana, et al.
Analytica Chimica Acta, 494.1, 187-197 (2003)
Christian Dye
Bronopol, Resorcinol, m-Cresol and Triclosan in the Nordic Environment, 20-20 (2007)
Pichiah Saravanan et al.
Journal of environmental sciences (China), 20(12), 1508-1513 (2009-02-13)
An acclimatized mixed microbial culture, predominantly Pseudomonas sp., was enriched from a sewage treatment plant, and its potential to simultaneously degrade mixtures of phenol and m-cresol was investigated during its growth in batch shake flasks. A 2(2) full factorial design
Agnieszka Iwan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 66(4-5), 1030-1041 (2006-07-29)
Imines (ketimines and azomethines) derived from p-dibenzoylbenzene (DB) and terephthalic aldehyde (TA) and two aromatic amines: aniline and 2,6-dimethylaniline have been investigated. Compounds were synthesized via condensation of amines with carbonyl monomers in DMA or amine solution. When using DMA
G D Smith et al.
Acta crystallographica. Section D, Biological crystallography, 56(Pt 12), 1541-1548 (2000-11-28)
The structures of three R(6) human insulin hexamers have been determined. Crystals of monoclinic m-cresol-insulin, monoclinic resorcinol-insulin and rhombohedral m-cresol-insulin diffracted to 1. 9, 1.9 and 1.78 A, respectively, and have been refined to residuals of 0.195, 0.179 and 0.200

Protocols

Analytical standard separation of various phenols for research and industrial applications.

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