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45808

Supelco

Tricyclazol

PESTANAL®, analytical standard

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About This Item

Fórmula empírica (notación de Hill):
C9H7N3S
Número de CAS:
41814-78-2
Peso molecular:
189.24
Beilstein/REAXYS Number:
980261
EC Number:
255-559-5
MDL number:
MFCD00072466
UNSPSC Code:
41116107
PubChem Substance ID:
329756965
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

Cc1cccc2sc3nncn3c12

InChI

1S/C9H7N3S/c1-6-3-2-4-7-8(6)12-5-10-11-9(12)13-7/h2-5H,1H3

InChI key

DQJCHOQLCLEDLL-UHFFFAOYSA-N

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General description

Tricyclazole is a protectant, systemic fungicide, extensively used for the control of rice blast.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Tricyclazole may be used as an analytical reference standard for the quantification of the analyte in environmental samples using solid phase extrcation followed by liquid chromatography.

Legal Information

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

pictograms

Skull and crossbones
GHS06

signalword

Danger

hcodes

H301,H412

Hazard Classifications

Acute Tox. 3 Oral - Aquatic Chronic 3

Storage Class

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

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

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Certificados de análisis (COA)

Lot/Batch Number
BCCH6717
BCBW4716
SZBD077XV
SZBA055XV
SZBA055X

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Marcel M L Cunha et al.
BMC microbiology, 10, 80-80 (2010-03-18)
The pathogenic fungus Fonsecaea pedrosoi constitutively produces the pigment melanin, an important virulence factor in fungi. Melanin is incorporated in the cell wall structure and provides chemical and physical protection for the fungus.We evaluated the production of nitric oxide (NO)
Encarna Sancho et al.
Comparative biochemistry and physiology. Toxicology & pharmacology : CBP, 150(1), 25-32 (2009-02-17)
Short-term effects of tricyclazole on male zebrafish (Danio rerio) physiology were examined joint to the degree of recovery after exposure. Fish were exposed to 142 microg/L (1/100 LC(50)-96 h) of tricyclazole for 7 (Exp.1) and 14 days (Exp.2) and then
Ji Liu et al.
Biodegradation, 19(5), 695-703 (2008-01-15)
To assess the co-catabolism of phenanthrene and tricyclazole in different samples, the interaction during the degradation of phenanthrene and tricyclazole were investigated in medium, soil and soil/spent mushroom compost (SMC) mixture. Generally, tricyclazole showed a negative influence on the activity
Rodrigo Almeida-Paes et al.
Microbes and infection, 11(5), 554-562 (2009-03-31)
Sporothrix schenckii is known to produce DHN melanin on both conidial and yeast cells, however little information is available regarding the factors inducing fungal melanization. We evaluated whether culture conditions influenced melanization of 25 Brazilian S. schenckii strains and one
Hua-Xin Zhang et al.
Journal of fluorescence, 16(3), 287-294 (2006-06-23)
The interaction of tricyclazole (TCZ) with beta-cyclodextrin (beta-CD) and human serum albumin (HSA) were studied by fluorescence spectrum, UV-visible spectrum and second-order scattering technology. It was shown that TCZ has quite a strong ability to quench the fluorescence launching from
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