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2597-11-7

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2597-11-7 Usage

Description

1-HYDROXYCHLORDENE, also known as Chlordene Hydroxide, is a metabolite of heptachlor, an organochlorine pesticide and insecticide. It is derived from the breakdown of heptachlor, which was historically used in agriculture for the protection of crops from pests. The compound possesses unique chemical properties that make it a subject of interest in various applications.

Uses

Used in Agricultural Industry:
1-HYDROXYCHLORDENE is used as a metabolite in the process of pesticide degradation for [application reason]. The expression is: 1-HYDROXYCHLORDENE is used as a metabolite in the Agricultural Industry for the degradation and breakdown of heptachlor pesticides, reducing their environmental impact and potential harm to non-target organisms.
Used in Environmental Research:
1-HYDROXYCHLORDENE is used as a biomarker for [application reason]. The expression is: 1-HYDROXYCHLORDENE is used as a biomarker in Environmental Research for monitoring the presence and degradation of heptachlor and related organochlorine pesticides in the environment, providing valuable data on their ecological impact and persistence.
Used in Toxicology Studies:
1-HYDROXYCHLORDENE is used as a compound of interest in [application reason]. The expression is: 1-HYDROXYCHLORDENE is used as a compound of interest in Toxicology Studies for understanding its potential toxic effects on human health and the environment, as well as its role in the overall toxicity of heptachlor and its related compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 2597-11-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,9 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2597-11:
(6*2)+(5*5)+(4*9)+(3*7)+(2*1)+(1*1)=97
97 % 10 = 7
So 2597-11-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H6Cl6O/c11-6-7(12)9(14)5-3(1-2-4(5)17)8(6,13)10(9,15)16/h1-5,17H

2597-11-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,7,8,9,10,10-Hexachlorotricyclo[5.2.1.0<sup>2,6</sup>]deca-4,8-dien-3-ol

1.2 Other means of identification

Product number -
Other names 1-hydroxy-1H-quinoxaline-2-thione

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2597-11-7 SDS

2597-11-7Upstream product

2597-11-7Relevant articles and documents

Miyazaki et al.

, p. 975 (1978)

NMR spectroscopy in environmental chemistry: 1H and 13C NMR parameters of tricyclic polychlorinated C10 hydrocarbons and their oxy derivatives based on two-dimensional NMR techniques

Kolehmainen, Erkki,Koivisto, Jari,Laihia, Katri,Kauppinen, Reijo,Paasivirta, Jaakko

, p. 359 - 364 (1999)

Two-dimensional homo-and heteronuclear NMR chemical shift correlation techniques were applied in the characterization of five tricyclic polychlorinated C10 hydrocarbons, chlordene (1), heptachlor (2), rrans-nonachlor (3), α-chlordene (4) and γ-chlordene (5), which are spread globally in the environment owing to their use as insecticides. Approximate and partly contradictory 1H and 13C NMR chemical shifts reported in the literature were corrected in this work. The chemical shift assignments of 1-5 were based on DQF COSY, HMQC and HMBC experiments. In addition, an INADEQUATE experiment was needed to ascertain the 13C chemical shifts assignment of 2. The n J(H,H)s of 1-5 were solved by computer-assisted spectral analyses. Further, complete 1H and 13C NMR parameter sets of three oxy derivatives, heptachlor exo-epoxide (6), 1-exo-hydroxychlordene (7) and its acetate (8), were also determined. Compounds 7 and 8 were synthesized to be used as model compounds, and their NMR parameters are reported for the first time. By using solvent susceptibility matched symmetrical micro-NMR tubes and HMQC and HMBC experiments, 1-5 can be reliably characterized at submilligram levels by their 1H and 13C NMR parameters with a 500 MHz (11.8T) spectrometer and a 5 mm diameter standard probehead. Copyright

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