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M34006

Sigma-Aldrich

3-Methylcatechol

98%

Synonym(s):

1,2-Dihydroxy-3-methylbenzene, 2,3-Dihydroxytoluene, 2,3-Toluenediol, 2-Hydroxy-3-methylphenol, 2-Hydroxy-6-methylphenol, 3-Methyl-1,2-benzenediol, 3-Methyl-1,2-dihydroxybenzene, 3-Methylpyrocatechol

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About This Item

Linear Formula:
CH3C6H3-1,2-(OH)2
CAS Number:
488-17-5
Molecular Weight:
124.14
EC Number:
207-672-6
MDL number:
MFCD00016435
UNSPSC Code:
12352100
PubChem Substance ID:
24896838
NACRES:
NA.22

Assay

98%

bp

241 °C (lit.)

mp

65-68 °C (lit.)

shipped in

wet ice

storage temp.

2-8°C

SMILES string

Cc1cccc(O)c1O

InChI

1S/C7H8O2/c1-5-3-2-4-6(8)7(5)9/h2-4,8-9H,1H3

InChI key

PGSWEKYNAOWQDF-UHFFFAOYSA-N

Related Categories

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H317,H319,H335

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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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M G Wallis et al.
The Biochemical journal, 266(2), 605-609 (1990-03-01)
A purification procedure has been developed for an extradiol dioxygenase expressed in Escherichia coli, which was originally derived from a Pseudomonas putida strain able to grow on toluidine. Physical and kinetic properties of the enzyme have been investigated. The enzyme
P Cerdan et al.
Journal of bacteriology, 176(19), 6074-6081 (1994-10-01)
Catechol 2,3-dioxygenase encoded by TOL plasmid pWW0 of Pseudomonas putida consists of four identical subunits, each containing one ferrous ion. The enzyme catalyzes ring cleavage of catechol, 3-methylcatechol, and 4-methylcatechol but shows only weak activity toward 4-ethylcatechol. Two mutants of
Arved E Reising et al.
Journal of chromatography. A, 1436, 118-132 (2016-02-10)
Lateral transcolumn heterogeneities and the presence of larger voids in a packing (comparable to the particle size) can limit the preparation of efficient chromatographic columns. Optimizing and understanding the packing process provides keys to better packing structures and column performance.
M S Shields et al.
Applied and environmental microbiology, 57(7), 1935-1941 (1991-07-01)
Pseudomonas cepacia G4 possesses a novel pathway of toluene catabolism that is shown to be responsible for the degradation of trichloroethylene (TCE). This pathway involves conversion of toluene via o-cresol to 3-methylcatechol. In order to determine the enzyme of toluene
Raúl Muñoz et al.
Biodegradation, 19(6), 897-908 (2008-04-15)
The response of Pseudomonas putida F1 to process fluctuations and operational failures during toluene biodegradation was evaluated in a chemostat suspended growth bioreactor. The ability of P. putida F1 to rapidly increase its specific toluene degradation capacity resulted in no
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