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65996

Supelco

m-Cresol

analytical standard

Synonym(e):

1-Hydroxy-3-meththylbenzol, 3-Hydroxytoluen, 3-Methylphenol

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About This Item

Lineare Formel:
CH3C6H4OH
CAS-Nummer:
108-39-4
Molekulargewicht:
108.14
Beilstein:
506719
EG-Nummer:
203-577-9
MDL-Nummer:
MFCD00002302
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329760142
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

100

Dampfdichte

3.72 (vs air)

Dampfdruck

<1 mmHg ( 20 °C)

Assay

≥99.0% (GC)

Selbstzündungstemp.

1036 °F

Haltbarkeit

limited shelf life, expiry date on the label

Expl.-Gr.

1.06-1.35 %, 150 °F

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Brechungsindex

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

bp

203 °C (lit.)

mp (Schmelzpunkt)

8-10 °C (lit.)

Dichte

1.034 g/mL at 25 °C (lit.)

Anwendung(en)

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

Format

neat

SMILES String

Cc1cccc(O)c1

InChI

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

InChIKey

RLSSMJSEOOYNOY-UHFFFAOYSA-N

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Allgemeine Beschreibung

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.

Anwendung

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.

Piktogramme

Skull and crossbonesCorrosion
GHS06,GHS05

Signalwort

Danger

Gefahreneinstufungen

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

WGK

WGK 2

Flammpunkt (°F)

186.8 °F

Flammpunkt (°C)

86 °C

Persönliche Schutzausrüstung

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

Choose from one of the most recent versions:

Analysenzertifikate (COA)

Lot/Batch Number
BCCC8353
BCCC9465
BCCC9464
BCCB2265
BCBW3996

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o-Cresol ReagentPlus&#174;, &#8805;99%

Sigma-Aldrich

C85700

o-Cresol

2,5-Dichlorbenzylalkohol 99%

Sigma-Aldrich

183601

2,5-Dichlorbenzylalkohol

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

Sigma-Aldrich

448192

m-Kresol-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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Artikel

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

Protokolle

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

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 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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