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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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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.
George P Prpich et al.
Biotechnology and bioengineering, 98(5), 1008-1016 (2007-04-28)
The bioproduction of 3-methylcatechol from toluene via Pseudomonas putida MC2 was performed in a solid-liquid two-phase partitioning bioreactor with the intent of increasing yield and productivity over a single-phase system. The solid phase consisted of HYTREL, a thermoplastic polymer that
L E Hüsken et al.
Applied microbiology and biotechnology, 55(5), 571-577 (2001-06-21)
The bioconversion of toluene into 3-methylcatechol was studied as a model system for the production of valuable 3-substituted catechols in general. For this purpose, an improved microbial system for the production of 3-methylcatechol was obtained. Pseudomonas putida strains containing the
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
Anna Andolfi et al.
Journal of natural products, 75(10), 1785-1791 (2012-10-11)
Two isolates of Neofusicoccum australe belonging to ITS haplotypes H4 and H1 and associated with grapevine cordon dieback and branch dieback of Phoenicean juniper, respectively, have been shown to produce in vitro structurally different secondary metabolites. From the strain BOT48
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