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05-6450

Sigma-Aldrich

Cresol mixture of isomers

CP

Synonym(s):

Methylphenol tricresol

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About This Item

CAS Number:
1319-77-3
MDL number:
MFCD00151099
UNSPSC Code:
12352002
PubChem Substance ID:
329748135

grade

CP

form

liquid

availability

available only in Japan

SMILES string

Cc1ccc(O)cc1.Cc2cccc(O)c2.Cc3ccccc3O

InChI

1S/3C7H8O/c1-6-2-4-7(8)5-3-6;1-6-3-2-4-7(8)5-6;1-6-4-2-3-5-7(6)8/h3*2-5,8H,1H3

InChI key

QTWJRLJHJPIABL-UHFFFAOYSA-N

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pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

signalword

Danger

Hazard Classifications

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

Storage Class

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

wgk_germany

WGK 2

flash_point_f

199.4 °F - closed cup

flash_point_c

93 °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’.

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Z Alexieva et al.
Journal of industrial microbiology & biotechnology, 35(11), 1297-1301 (2008-08-21)
Most industrial wastes contain different organic mixtures, making important the investigation on the microbial destruction of composite substrates. The capability of microbes to remove harmful chemicals from polluted environments strongly depends on the presence of other carbon and energy substrates.
Zlatka Alexieva et al.
Biodegradation, 21(4), 625-635 (2010-02-04)
The ability of the white rot fungus Trametes versicolor strain 1 to degrade and utilize methylated phenols (cresols) was established for the first time in a medium not containing any other carbon components. The data obtained demonstrated the better potential
Chen-Ken Seak et al.
Clinical toxicology (Philadelphia, Pa.), 48(9), 959-960 (2010-10-07)
Cresol is a phenol derivative used as a disinfectant worldwide. Acute cresol poisoning is potentially fatal as it may cause multiple organ failure. We present a case of acute cresol intoxication in a male patient to illustrate the effects of
I E Katina et al.
Biofizika, 53(6), 1078-1086 (2009-01-14)
A comparative analysis of contractile responses evoked by acetylcholine and external sodium removal in twitch and tonic frog skeletal muscle fibers has been performed. To elucidate the possible differences in the participation of various mechanisms of Ca2+ homeostasis in the
Himansu S Biswal et al.
The Journal of chemical physics, 129(18), 184311-184311 (2008-12-03)
Experimental evidence is presented for the O-H-S hydrogen bonding in the complexes of simple model compounds of methionine (dimethyl sulphide) and tyrosine (phenol, p-cresol, and 2-naphthol). The complexes were formed in the supersonic jet and were detected using resonantly enhanced
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