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Merck
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32431

Supelco

解草噁唑

PESTANAL®, analytical standard

同義詞:

(RS)-3-Dichloroacetyl-5-(2-furanyl)-2,2-dimethyl-1,3-oxazolidine

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About This Item

經驗公式(希爾表示法):
C11H13Cl2NO3
CAS號碼:
分子量::
278.13
Beilstein:
11343170
MDL號碼:
分類程式碼代碼:
41116107
PubChem物質ID:
NACRES:
NA.24
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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

應用

agriculture
environmental

形式

neat

儲存溫度

2-8°C

SMILES 字串

CC1(C)OC(CN1C(=O)C(Cl)Cl)c2ccco2

InChI

1S/C11H13Cl2NO3/c1-11(2)14(10(15)9(12)13)6-8(17-11)7-4-3-5-16-7/h3-5,8-9H,6H2,1-2H3

InChI 密鑰

MCNOFYBITGAAGM-UHFFFAOYSA-N

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相關類別

一般說明

Furilazole is classified under the dichloroacetamide group of herbicide safeners.[1]

應用

Furilazole may be used as an analytical reference standard for the determination of the analyte in:
  • Vegetables[2][3] and a fruit samples[2] by solid-phase extraction (SPE) and gas chromatography/multiphoton ionization/time-of-flight mass spectrometry (GC/MPI/TOFMS) as well as GC coupled to electron ionization (EI) MS.
  • Food samples by GC/MS with multiple reaction monitoring (MRM) detection.[4]

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

推薦產品

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

法律資訊

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

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Oral

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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分析證明 (COA)

Lot/Batch Number

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存取文件庫

Solubility, partitioning, oxidation and photodegradation of dichloroacetamide herbicide safeners, benoxacor and furilazole.
Acharya SP and Weidhaas J
Chemosphere, 211, 1018-1024 (2018)
Ionization of pesticides using a far-ultraviolet femtosecond laser in gas chromatography/time-of-flight mass spectrometry.
Hashiguchi Y, et al.
Analytical and Bioanalytical Chemistry, 405(22), 7053-7059 (2013)
Compensation of matrix effects in gas chromatography-mass spectrometry analysis of pesticides using a combination of matrix matching and multiple isotopically labeled internal standards.
Tsuchiyama T, et al.
Journal of Chromatography A, 1524(22), 233-245 (2017)
Analysis of pesticides by gas chromatography/multiphoton ionization/mass spectrometry using a femtosecond laser.
Li A, et al.
Analytica Chimica Acta, 701(1), 52-59 (2011)
Md Shiful Islam et al.
Gene, 639, 149-162 (2017-10-11)
Glutathione S-transferases (GSTs) are ubiquitous enzymes which play versatile functions including cellular detoxification and stress tolerance. In this study, a comprehensive genome-wide identification of GST gene family was carried out in potato (Solanum tuberosum L.). The result demonstrated the presence

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