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Merck

45434

Supelco

二氯萘醌

PESTANAL®, analytical standard

别名:

2,3-二氯-1,4-萘醌, 二氯萘醌

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About This Item

经验公式(希尔记法):
C10H4Cl2O2
CAS号:
分子量:
227.04
Beilstein:
1073511
EC號碼:
MDL號碼:
分類程式碼代碼:
41116107
PubChem物質ID:
NACRES:
NA.24

等級

analytical standard

品質等級

產品線

PESTANAL®

儲存期限

limited shelf life, expiry date on the label

技術

HPLC: suitable
gas chromatography (GC): suitable

mp

194-197 °C (lit.)

應用

agriculture
environmental

格式

neat

SMILES 字串

ClC1=C(Cl)C(=O)c2ccccc2C1=O

InChI

1S/C10H4Cl2O2/c11-7-8(12)10(14)6-4-2-1-3-5(6)9(7)13/h1-4H

InChI 密鑰

SVPKNMBRVBMTLB-UHFFFAOYSA-N

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一般說明

Dichlon is an agricultural fungicide of the quinone class, widely used against a variety of plant pathogenic fungi.

應用

Dichlon may be used as an analytical reference standard for the quantification of the analyte in food matrices using supercritical fluid extraction (SFE) and supercritical fluid chromatography (SFC).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

法律資訊

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

象形圖

Skull and crossbonesEnvironment

訊號詞

Danger

危險分類

Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2

儲存類別代碼

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

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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分析证书(COA)

Lot/Batch Number

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If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

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在文件库中查找您最近购买产品的文档。

访问文档库

Chemistry and Biology of Water, Air and Soil: Environmental Aspects
Studies in Environmental Science, 53(3), 1314-1326 (1993)
Pesticide residues in canned foods, fruits, and vegetables: The application of supercritical fluid extraction and chromatographic techniques in the analysis
EL-Saeid.HM
TheScientificWorldJournal, 3(3), 1314-1326 (2003)
Thin-layer chromatography of some substituted naphthoquinones
Agricultural and Biological Chemistry, 30(9), 935-936 (1966)
Angupillai Satheshkumar et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 98, 378-383 (2012-09-18)
Various spectroscopy techniques (UV-Vis, DRS, FT-IR, (1)H NMR, LC-MS) and theoretical computations have been employed to investigate the mechanism of the nucleophilic substitution reaction of 2,3-dichloronaphthoquinone (DCNQ) with para-substituted anilines in solid state under base- and solvent-free conditions against traditional
M Alnabari et al.
Amino acids, 20(4), 381-387 (2001-07-17)
Chloranil and 2,3-dichloro-1,4-naphthoquinone have been linked to different natural and unnatural amino acids via a vinylic spacer. Two routes were developed for the facile preparation of these novel modified amino acids: the direct method, which can only be applied to

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