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250 MG
₩189,501
About This Item
실험식(Hill 표기법):
C10H14Cl6N4O2
CAS Number:
Molecular Weight:
434.96
Beilstein:
626358
EC Number:
MDL number:
UNSPSC 코드:
41116107
PubChem Substance ID:
NACRES:
NA.24
추천 제품
Grade
analytical standard
Quality Level
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
SMILES string
ClC(Cl)(Cl)C(NC=O)N1CCN(CC1)C(NC=O)C(Cl)(Cl)Cl
InChI
1S/C10H14Cl6N4O2/c11-9(12,13)7(17-5-21)19-1-2-20(4-3-19)8(18-6-22)10(14,15)16/h5-8H,1-4H2,(H,17,21)(H,18,22)
InChI key
RROQIUMZODEXOR-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
Triforin is a systemic fungicide, commonly used for the control of scab, petal blight, brown rot, black spot, rust and other diseases affecting fruits and vegetables.[1]
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
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Inhalation - Aquatic Chronic 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
가장 최신 버전 중 하나를 선택하세요:
Sittig's Handbook of Pesticides and Agricultural Chemicals, 11(2), 506-513 (2014)
Method validation for the analysis of pesticide residues in grain by thin-layer chromatography
Tiryaki.O
Accreditation and Quality Assurance, 11(10), 506-513 (2006)
[Determination of triforin in water and soil by a thin-layer chromatographic method].
P Iu Iurgaĭtene et al.
Gigiena i sanitariia, (1)(1), 46-47 (1981-01-01)
J R Ptashekas
Journal of environmental pathology, toxicology and oncology : official organ of the International Society for Environmental Toxicology and Cancer, 10(6), 297-300 (1990-11-01)
Environmental chemical agents usually affect the human organism in combination rather than alone. The objective of this study was to determine the effect on the gastric mucosa of the herbicide Saprol alone or in combination with the nitroso compound sodium
V N Golubev et al.
Biofizika, 34(1), 42-44 (1989-01-01)
It is found that bilayer lipid membranes acquire little cationic selectivity in the presence of systemic fungicide triforine at physiological pH, and besides potassium selectivity exceeds the sodium one. A decrease of pH to 3.5 leads to substitution of cationic
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