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Key Documents

40018

Supelco

2-Chloronaphthalene solution

certified reference material, 5000 μg/mL in methanol

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About This Item

CAS Number:
91-58-7
EC Number:
200-659-6
UNSPSC Code:
41116105

grade

certified reference material
TraceCERT®

Quality Level

100

CofA

certificate of analysis is enclosed in each package.

packaging

ampule of 1 mL

concentration

5000 μg/mL in methanol

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

environmental

format

single component solution

storage temp.

2-8°C

InChI

1S/C10H7Cl/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7H

InChI key

CGYGETOMCSJHJU-UHFFFAOYSA-N

Application

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

Legal Information

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

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

target_organs

Eyes

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

51.8 °F - closed cup

flash_point_c

11 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
XA17178V
XA17168V
LC12790
LC01368
LB82171

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Alok Sinha et al.
Journal of colloid and interface science, 314(2), 552-561 (2007-06-19)
Interaction of 2-chloronaphthalene (2-CN) with high-carbon iron filings (HCIF) was studied in anaerobic batch systems, both under well-mixed and poorly-mixed conditions. In well-mixed conditions, partitioning of 2-CN between solid and aqueous phases was fast, resulting in rapid attainment of equilibrium.
D A Williamson et al.
Chemosphere, 40(12), 1443-1446 (2000-05-02)
Photoexcitation of complexes between cyclophane 1 and 1- or 2-chloronaphthalene in aqueous solution leads to rapid dechlorination of the guest, a reaction driven by electron transfer from host to excited guest. The main photoproducts contain a naphthyl group covalently attached
T Mori et al.
Applied microbiology and biotechnology, 61(4), 380-383 (2003-05-14)
The biodegradation of chloronaphthalene (CN) and polycyclic aromatic hydrocarbons by the white-rot fungus Phlebia lindtneri, which can degrade dichlorinated dioxins and non-chlorinated dioxin-like compounds, was investigated. Naphthalene, phenanthrene, 1-chloronaphthalene (1-CN) and 2-chloronaphthalene (2-CN) were metabolized by the fungus to form

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