추천 제품
Grade
certified reference material
Quality Level
grade
TraceCERT®
CofA
certificate of analysis is enclosed in each package.
포장
ampule of 1 mL
농도
5000 μg/mL in methanol
기술
HPLC: suitable
gas chromatography (GC): suitable
응용 분야
environmental
형식
single component solution
저장 온도
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
애플리케이션
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
법적 정보
TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1
표적 기관
Eyes
Storage Class Code
3 - Flammable liquids
WGK
WGK 2
Flash Point (°F)
51.8 °F - closed cup
Flash Point (°C)
11 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves
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.
Guest dechlorination and covalent capture following photoexcitation of inclusion complexes in water.
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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