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Merck

36747

Supelco

3-Chlorphenol

PESTANAL®, analytical standard

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About This Item

Lineare Formel:
ClC6H4OH
CAS-Nummer:
Molekulargewicht:
128.56
Beilstein:
1634401
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:

Qualität

analytical standard

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Brechungsindex

n20/D 1.563 (lit.)

bp

214 °C (lit.)

mp (Schmelzpunkt)

31-34 °C (lit.)

Dichte

1.218 g/mL at 25 °C (lit.)

Anwendung(en)

agriculture
environmental

Format

neat

SMILES String

Oc1cccc(Cl)c1

InChI

1S/C6H5ClO/c7-5-2-1-3-6(8)4-5/h1-4,8H

InChIKey

HORNXRXVQWOLPJ-UHFFFAOYSA-N

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Anwendung

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Rechtliche Hinweise

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

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Irrit. 2

Lagerklassenschlüssel

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 2

Flammpunkt (°F)

248.0 °F - closed cup

Flammpunkt (°C)

120 °C - closed cup

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves


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Analysenzertifikate (COA)

Lot/Batch Number

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Stefano M Marino et al.
Archives of biochemistry and biophysics, 505(1), 67-74 (2010-09-30)
Tyrosinase (Ty) is a copper-containing enzyme ubiquitously distributed in nature. In recent years, Ty has attracted interest as a potential detoxifying agent for xenobiotic compounds with phenolic structure. Among these, chlorophenols are particularly relevant pollutants, commonly found in waste waters.
Clarissa A Olivati et al.
Bioprocess and biosystems engineering, 32(1), 41-46 (2008-04-15)
Langmuir-Blodgett (LB) and layer-by-layer films (LbL) of a PPV (p-phenylenevinylene) derivative, an azo compound and tetrasulfonated phthalocyanines were successfully employed as transducers in an "electronic tongue" system for detecting trace levels of phenolic compounds in water. The choice of the
S H Lin et al.
Waste management (New York, N.Y.), 22(6), 595-603 (2002-09-07)
Experimental investigations were conducted on the adsorption characteristics of phenol and m-chlorophenol by organobentonites. The organobentonites were prepared by modifying natural bentonite with various quaternary ammonium salts including tetramethylammonium bromide, hexadecyltrimethylammonium bromide, benzyl-triethylammonium bromide, tetraethylammonium bromide and cetylpyridinium bromide. The
Neng-Chou Shang et al.
Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering, 37(2), 261-271 (2002-02-16)
This study investigates the variation of toxicity during ozonation of 2-chlorophenol (2-CP), 3-chlorophenol (3-CP) and 4-chlorophenol (4-CP) in neutral condition. Acute toxicity of pure chlorophenols (CPs) and their ozonated intermediates was evaluated by Microtox assay. The results revealed that the
Hideo Utsumi et al.
Water research, 37(20), 4924-4928 (2003-11-08)
Hydroxyl (OH) radical is proposed as an important factor in the ozonation of water. In the present study, the enhancing effect of 3-chlorophenol on OH radical generation was mathematically evaluated using electron spin resonance (ESR)/spin-trapping technique. OH radical was trapped

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