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Merck
모든 사진(1)

주요 문서

36500

Supelco

Dialifos

PESTANAL®, analytical standard

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About This Item

실험식(Hill 표기법):
C14H17ClNO4PS2
CAS Number:
Molecular Weight:
393.85
Beilstein:
1550800
EC Number:
MDL number:
UNSPSC 코드:
41116107
PubChem Substance ID:
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Grade

analytical standard

제품 라인

PESTANAL®

유통기한

limited shelf life, expiry date on the label

기술

HPLC: suitable
gas chromatography (GC): suitable

응용 분야

agriculture
environmental

형식

neat

저장 온도

2-8°C

SMILES string

CCOP(=S)(OCC)SC(CCl)N1C(=O)c2ccccc2C1=O

InChI

1S/C14H17ClNO4PS2/c1-3-19-21(22,20-4-2)23-12(9-15)16-13(17)10-7-5-6-8-11(10)14(16)18/h5-8,12H,3-4,9H2,1-2H3

InChI key

MUMQYXACQUZOFP-UHFFFAOYSA-N

유사한 제품을 찾으십니까? 방문 제품 비교 안내

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

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

픽토그램

Skull and crossbonesEnvironment

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 1 Dermal - Acute Tox. 1 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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시험 성적서(COA)

Lot/Batch Number

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이 제품을 이미 가지고 계십니까?

문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

M Kalafatić et al.
The International journal of developmental biology, 35(3), 335-340 (1991-09-01)
Investigations showed that the three insecticides used had the most damaging effect upon hydra immediately after treatment. The tentacles and the hypostome are the parts most often damaged. Inse the affected cells, lesions appear in the intracellular membranes, the nucleus
Prashant Shankarrao Adole et al.
Analytical biochemistry, 621, 114158-114158 (2021-03-12)
Intentional or unintentional intake of anticholinesterase pesticides became common due to their extensive use in agricultural and domestic purposes, resulting in numerous poisoning cases. A simple, accurate, and sensitive gas chromatography-ion trap mass spectrometry-based method for the quantification of 12
Environmental fate of dialifor and formation of its oxygen analogue following application on grape vines in the San Joaquin Valley, California.
W Winterlin et al.
Journal of agricultural and food chemistry, 28(6), 1078-1083 (1980-11-01)
R Besser et al.
Neurology, 40(8), 1275-1277 (1990-08-01)
Two patients with acute severe organophosphate intoxication showed (1) single evoked compound muscle action potentials (CMAP) with repetitive discharges and (2) prominent decremental responses of CMAP with 20 and 50 Hz supramaximal nerve stimulation. Following the intravenous injection of single
H N Nigg et al.
Archives of environmental contamination and toxicology, 10(4), 497-504 (1981-07-01)
Surface residue disappearance rates of dioxathion, malathion, oxydemetonmethyl, and dialifor were the same for fruit and leaves, and they increase with temperature. Disappearance rates were in the order of malathion greater than or equal to oxydemetonmethyl greater than dialifor greater

질문

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