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03869

Sigma-Aldrich

Cresol mixture of isomers

technical, crude, ~85% (sum of isomers, GC)

Synonym(s):

Methylphenol tricresol

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About This Item

CAS Number:
1319-77-3
MDL number:
MFCD00151099
UNSPSC Code:
12352100
PubChem Substance ID:
329747827
NACRES:
NA.22

grade

technical

Quality Level

200

Assay

~85% (sum of isomers, GC)

form

liquid

quality

crude

impurities

≤8% phenol (GC)

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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Related Categories

Application


  • Separation of cresols using coelectroosmotic capillary electrophoresis.: This research explores the separation of cresol isomers using coelectroosmotic capillary electrophoresis. The study demonstrates an efficient method for analyzing cresol mixtures, which is valuable in both industrial and pharmaceutical applications where precise separation of isomers is critical (Masselter et al., 1993).

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Muta. 2 - 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)

176.0 °F - closed cup

Flash Point(C)

80 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL6755
BCCK9914
BCCH7369
BCCD3670
WXBC7542V

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P-I-A-N-O Kit

Cresol red indicator grade, Dye content 95 %

Sigma-Aldrich

114472

Cresol red

o-Xylene analytical standard

Supelco

95660

o-Xylene

Xylenes reagent grade

Sigma-Aldrich

214736

Xylenes

Xylenes ACS reagent, ≥98.5% xylenes + ethylbenzene basis

Sigma-Aldrich

247642

Xylenes

Martin R Challand et al.
The Journal of biological chemistry, 285(8), 5240-5248 (2009-11-20)
Thiazole synthase in Escherichia coli is an alphabeta heterodimer of ThiG and ThiH. ThiH is a tyrosine lyase that cleaves the C alpha-C beta bond of tyrosine, generating p-cresol as a by-product, to form dehydroglycine. This reactive intermediate acts as
Tao You et al.
Huan jing ke xue= Huanjing kexue, 30(6), 1744-1748 (2009-08-11)
Simulated wastewater containing o-, m- and p-cresol was used respectively to study the effects of substituted position on adsorption and desorption and the feasibility of activated carbon adsorption-bioregeneration treatment. According to the isotherm, the adsorbability sequences in the order of
Duu-Jong Lee et al.
Applied microbiology and biotechnology, 89(1), 209-215 (2010-09-21)
High-strength cresol isomers were treated with phenol-acclimated granules in batch experiments. The aerobic granules effectively metabolized cresol isomers at concentrations up to 1,500 mg l(-1). The modified Haldane kinetic model, used to assess the kinetic behavior during cresol degradation by
Ping Wang et al.
Journal of environmental sciences (China), 21(6), 821-826 (2009-10-07)
The changes of microbial community structures and functional genes during the biodegradation of single phenol and phenol plus p-cresol under high salt condition were explored. It was found that the phenol-fed system (PFS) exhibited stronger degrading abilities and more stable
Koji Okamoto et al.
BMJ case reports, 2011, doi:10-doi:10 (2011-01-01)
The authors report a case of a 43-year-old woman who presented with second degree chemical burns to 9% of the total body surface area due to cutaneous contact with cresol. This was associated with acute oliguric kidney injury requiring haemodialysis.
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