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D174009

Sigma-Aldrich

2,3-Dimethylphenol

98%

Synonyme(s) :

3-Hydroxyl-o-xylene, vic.-o-Xylenol

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About This Item

Formule linéaire :
(CH3)2C6H3OH
Numéro CAS:
Poids moléculaire :
122.16
Numéro Beilstein :
1906267
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22

Densité de vapeur

4.23 (vs air)

Pureté

98%

Forme

crystals

Point d'ébullition

217 °C (lit.)

Pf

70-73 °C (lit.)

Chaîne SMILES 

Cc1cccc(O)c1C

InChI

1S/C8H10O/c1-6-4-3-5-8(9)7(6)2/h3-5,9H,1-2H3

Clé InChI

QWBBPBRQALCEIZ-UHFFFAOYSA-N

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Application

  • Removal of phenolic compounds from aqueous solutions using poly (styrene-co-divinylbenzene) functionalized with aminophosphonic acid: This research explores the effectiveness of specific polymer adsorbents in removing 2,3-dimethylphenol from water (CM Davidescu et al., 2014).
  • Adsorption of phenol or phenol derivatives onto styrene-1%(15%) divinylbenzene polymeric adsorbents functionalized with aminopropyl (benzyl) phosphonic: Focuses on the removal of 2,3-dimethylphenol from aqueous solutions, highlighting the efficiency of newly developed adsorbents (R Ardelean et al., 2016).
  • Carpe diene! Europium-catalyzed and rearrangements of aryl-pentadienyl ethers: Describes a study where 2,3-dimethylphenol was used to test the catalytic properties of Europium in organic reactions (M Kaiser et al., 2023).

Pictogrammes

Skull and crossbonesCorrosionEnvironment

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B

Code de la classe de stockage

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

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

203.0 °F - closed cup

Point d'éclair (°C)

95 °C - closed cup

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges, type P3 (EN 143) respirator cartridges


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Consulter la Bibliothèque de documents

G Baggi et al.
Applied and environmental microbiology, 53(9), 2129-2132 (1987-09-01)
A Pseudomonas stutzeri strain capable of growing on o-xylene was isolated from enrichment cultures. The organism grew on 2,3- and 3,4-dimethylphenol but not on 2-methylbenzyl alcohol, o-tolualdehyde, or o-toluate. P. stutzeri was not able to utilize m-xylene, p-xylene, or 1,2,4-trimethylbenzene
A E Holliday et al.
Journal of chemical ecology, 38(3), 278-286 (2012-03-07)
The defensive secretion of the ground beetle Chlaenius cordicollis is predominantly 3-methylphenol. Adult C. cordicollis were collected in Pennsylvania and Manitoba and induced to discharge defensive secretion in a vial. The headspace was sampled by solid phase microextraction, and samples
Jee Hee Suh et al.
Chemical & pharmaceutical bulletin, 63(8), 573-578 (2015-06-05)
We describe the synthesis and biological evaluation of N-aryl-5-aryloxazol-2-amine derivatives that are able to inhibit 5-lipoxygenase (5-LOX), a key enzyme of leukotriene synthesis, for the treatment of inflammation-related diseases including asthma and rheumatoid arthritis. A novel structural moiety containing oxazole
Fangfang Zeng et al.
Insect biochemistry and molecular biology, 113, 103213-103213 (2019-08-24)
Mosquitoes rely heavily on the olfactory system to find a host for a bloodmeal, plants for a source of energy and suitable sites for oviposition. Here, we examined a cluster of eight odorant receptors (ORs), which includes one OR, CquiOR1
Zulin Zhang et al.
Journal of separation science, 37(24), 3699-3705 (2014-10-02)
A simple and rapid method was developed for the simultaneous analysis of nine different pesticides in water samples by gas chromatography with mass spectrometry. A number of parameters that may affect the recovery of pesticides, such as the type of

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