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65996

Supelco

m-Cresol

analytical standard

Sinônimo(s):

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

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About This Item

Fórmula linear:
CH3C6H4OH
Número CAS:
108-39-4
Peso molecular:
108.14
Beilstein:
506719
Número CE:
203-577-9
Número MDL:
MFCD00002302
Código UNSPSC:
41116107
ID de substância PubChem:
329760142
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

100

densidade de vapor

3.72 (vs air)

pressão de vapor

<1 mmHg ( 20 °C)

Ensaio

≥99.0% (GC)

temperatura de autoignição

1036 °F

prazo de validade

limited shelf life, expiry date on the label

Lim. expl.

1.06-1.35 %, 150 °F

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

índice de refração

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

p.e.

203 °C (lit.)

pf

8-10 °C (lit.)

densidade

1.034 g/mL at 25 °C (lit.)

aplicação(ões)

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

Formato

neat

cadeia de caracteres SMILES

Cc1cccc(O)c1

InChI

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

chave InChI

RLSSMJSEOOYNOY-UHFFFAOYSA-N

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Descrição geral

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.

Aplicação

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.

Pictogramas

Skull and crossbonesCorrosion
GHS06,GHS05

Palavra indicadora

Danger

Frases de perigo

H301 + H311,H314,H412

Classificações de perigo

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

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

186.8 °F - closed cup

Ponto de fulgor (°C)

86 °C - closed cup

Equipamento de proteção individual

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Certificados de análise (COA)

Lot/Batch Number
BCCC8353
BCCC9465
BCCC9464
BCCB2265
BCBW3996

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Se precisar de uma versão específica, você pode procurar um certificado específico pelo número do lote ou da remessa.

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2,5-Dichlorobenzyl alcohol 99%

Sigma-Aldrich

183601

2,5-Dichlorobenzyl alcohol

m-Cresol-d8 98 atom % D, 98% (CP)

Sigma-Aldrich

448192

m-Cresol-d8

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)
Chiu-Po Chan et al.
Toxicology, 208(1), 95-104 (2005-01-25)
Cresol is a well-known environmental pollutant, toluene metabolite, uremic toxicant and accidental poisoning product. Formocresol, a preparation of formalin and cresol, is also used as a root canal medicament and for pulpotomy of primary teeth. However, little is known about
P Saravanan et al.
Bioresource technology, 99(18), 8553-8558 (2008-05-13)
An internal loop airlift reactor (ILALR) is developed and studied for biodegradation of phenol/m-cresol as single and dual substrate systems under batch and fed batch operation using an indigenous mixed microbial strain, predominantly Pseudomonas sp. The results showed that the
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
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Artigos

US EPA Method 8041: GC Analysis of Phenols on Equity®-5

Separation of 2-Chlorophenol; 2,4-Dichlorophenol; 2,4,6-Tribromophenol; 2,4,6-Trichlorophenol; 2,4-Dinitrophenol; Pentafluorophenol; 2-Methylphenol, analytical standard; 2,3,4,6-Tetrachlorophenol; Pentachlorophenol; 4-Nitrophenol; 2-Bromophenol; 2,3,5,6-Tetrachlorophenol; 2,3,5-Trichlorophenol; 4-Chloro-3-methylphenol; 2,4,5-Trichlorophenol; 4-Methylphenol, analytical standard; 2,4-Dimethylphenol; 2-Nitrophenol; 3-Methylphenol, analytical standard; Phenol; 2-Methyl-4,6-dinitrophenol; 2,3,4-Trichlorophenol; 2,6-Dichlorophenol; 2,3,4,5-Tetrachlorophenol

Protocolos

HPLC Analysis of Cresols and Phenol on Astec® CYCLOBOND® I 2000

HPLC Analysis of Cresols and Phenol on Astec® CYCLOBOND® I 2000

GC Analysis of Phenols in Water on a 5% Phenyl Column after SPE using Supelclean™ ENVI-Chrom P

Separation of 2-Nitrophenol; Pentachlorophenol; 2-Bromophenol; Phenol; 4-Nitrophenol; 3-Methylphenol, analytical standard; 4-Chloro-3-methylphenol; 2,4-Dichlorophenol; 2,3,4,6-Tetrachlorophenol; 2-Methylphenol, analytical standard; 2,4,6-Trichlorophenol; 2,4-Dimethylphenol; 2-Chlorophenol

GC Analysis of Xylene Isomers on SLB®-IL60

GC Analysis of Xylene Isomers on SLB®-IL60 - The cresol (methylphenol) isomers are also precursors to many chemicals. This chromatogram of a mix of aromatic and methylphenol compounds was generated using an SLB-IL60 ionic liquid column. Its interaction mechanisms allow the separation of all three xylene isomers, and all three cresol isomers.

US EPA Method 8270 (Appendix IX): GC Analysis of Semivolatiles on Equity®-5 (30 m x 0.25 mm I.D., 0.50 μm)

US EPA Method 8270 (Appendix IX): GC Analysis of Semivolatiles on Equity®-5 (30 m x 0.25 mm I.D., 0.50 μm)

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