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Merck
CN

36715

Supelco

2,6-二甲基苯酚

PESTANAL®, analytical standard

别名:

2-羟基间二甲苯, 连间二甲苯酚

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关于此项目

线性分子式:
(CH3)2C6H3OH
化学文摘社编号:
576-26-1
分子量:
122.16
Beilstein:
1446677
EC 号:
209-400-1
MDL编号:
MFCD00002240
UNSPSC代码:
41116107
PubChem化学物质编号:
329755474
NACRES:
NA.24

主要文件

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等级

analytical standard

质量水平

100

产品线

PESTANAL®

自燃温度

1110 °F

保质期

limited shelf life, expiry date on the label

技术

HPLC: suitable
gas chromatography (GC): suitable

沸点

203 °C (lit.)

mp

43-45 °C (lit.)

应用

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

包装形式

neat

SMILES字符串

Cc1cccc(C)c1O

InChI

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

InChI key

NXXYKOUNUYWIHA-UHFFFAOYSA-N

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相关类别

一般描述

2,6-Dimethylphenol belongs to the class of phenols, commonly present in cigarette smoke and is a major toxic compound related to environmental and health issues.
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

应用

2,6-Dimethylphenol may be used as an analytical reference standard for the quantification of the analyte in mainstream cigarette smoke using gas chromatography coupled to mass spectrometry and high-performance liquid chromatography with fluorescence detection.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

其他说明

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

法律信息

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

警示用语：

Danger

危险分类

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

靶器官

Respiratory system

储存分类代码

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

WGK

WGK 3

闪点(°F)

186.8 °F - closed cup

闪点(°C)

86 °C - closed cup

个人防护装备

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

法规信息

危险化学品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCK5695
BCBZ9070

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Gas chromatography/mass spectrometry versus liquid chromatography/fluorescence detection in the analysis of phenols in mainstream cigarette smoke
Moldoveanu.CS and Kiser M
Journal of Chromatography A, 1141(1), 90-97 (2007)
E A Kemeleva et al.
Bioorganicheskaia khimiia, 34(4), 558-569 (2008-08-13)
Three new sulfur-containing derivatives of 2,6-dimethylphenol were synthesized. Their antioxidative activity, mutagenicity, and genotoxicity were examined by bacterial tests and by calculating the dominant lethal mutations in murine embryonic cells. It was shown that all the compounds synthesized have a
Tingting Li et al.
Talanta, 78(4-5), 1497-1502 (2009-04-14)
In the present work, a simple, selective, and sensitive method has been proposed for the determination of four phenols (catechol, resorcinol, 2,6-dimethylphenol, and 2,4,6-trinitrophenol) in water samples. The method is based on poly-(methacrylic acid-co-ethylene glycol dimethacrylate) monolith microextraction (PMME) and
Gertrud Haeseler et al.
British journal of pharmacology, 145(7), 916-925 (2005-05-25)
Phenol derivatives constitute a family of neuroactive compounds. The aim of our study was to identify structural features that determine their modulatory effects at glycine receptors. We investigated the effects of four methylated phenol derivatives and two halogenated analogues on
O Grech-Bélanger et al.
Research communications in chemical pathology and pharmacology, 58(1), 53-62 (1987-10-01)
A new metabolite, 2,6-dimethylphenol obtained by O-dealkylation of mexiletine by rabbit liver was identified. A g.c.-f.i.d. method was developed for its analysis in hepatic homogenates and some of the characteristics of the metabolic reaction were studied. Formation of 2,6-dimethylphenol is
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