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131983-72-7

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131983-72-7 Usage

Uses

Agricultural chemical.

Hazard

A reproductive hazard.

Agricultural Uses

Fungicide, Seed disinfectant: Used as a biocide in water-treatment facilities. Turf and seed protectant and treatment for grains, cereals, forage, fodder, straw, corn, barley, wheat to prevent rusts, powdery mildew and other pathogens. Registered for use in EU countries . Registered for use in the U.S. U.S. Maximum Allowable Residue Levels for the fungicide triticonazole from the treatment of seed prior to planting

Trade name

ALIOS?; CHARTER F2 FUNGICIDE SEED TREATMENT?; CHARTER FUNGICIDE SEED TREATMENT?; CHARTER PB FUNGICIDE SEED TREATMENT?; FUNGUS CLEAR ULTRA?; KINTO?; PREMIS 25 FS?; REAL?; RESERVE FUNGICIDE?; STAMINA F3 HL FUNGICIDE SEED TREATMENT?; STAMINA F3 RTU FUNGICIDE SEED TREATMENT?; TRITICONAZOLE CONCENTRATE FUNGICIDE?; TRITICONAZOLE 3 SC FUNGICIDE?; TRITICONAZOLE SC FUNGICIDE?; TRITICONAZOLE HL FUNGICIDE SEED TREATMENT?; TRITICONAZOLE 70 WDG FUNGICIDE?; TRITICONAZOLE TECHNICAL FUNGICIDE?

Check Digit Verification of cas no

The CAS Registry Mumber 131983-72-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,9,8 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 131983-72:
(8*1)+(7*3)+(6*1)+(5*9)+(4*8)+(3*3)+(2*7)+(1*2)=137
137 % 10 = 7
So 131983-72-7 is a valid CAS Registry Number.
InChI:InChI=1/C17H20ClN3O/c1-16(2)8-7-14(9-13-3-5-15(18)6-4-13)17(16,22)10-21-12-19-11-20-21/h3-6,9,11-12,22H,7-8,10H2,1-2H3/b14-9+

131983-72-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name triticonazole

1.2 Other means of identification

Product number -
Other names (5Z)-5-[(4-chlorophenyl)methylidene]-2,2-dimethyl-1-(1,2,4-triazol-1-ylmethyl)cyclopentan-1-ol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:131983-72-7 SDS

131983-72-7Upstream product

131983-72-7Downstream Products

131983-72-7Related news

Enantioseparation and determination of TRITICONAZOLE (cas 131983-72-7) enantiomers in fruits, vegetables, and soil using efficient extraction and clean-up methods07/29/2019

An efficient and novel enantioseparation and determination method was developed to quantify the enantiomers of chiral triazole fungicide triticonazole in fruit, vegetable, and soil samples. Under the optimal chromatographic conditions, the enantiomers of triticonazole were completely enantiosepa...detailed

Stereoselective quantification of TRITICONAZOLE (cas 131983-72-7) in vegetables by supercritical fluid chromatography07/28/2019

A highly fast analytical method though supercritical fluid chromatography (SFC) has been developed to quantify triticonazole enantiomers in cucumbers and tomatoes. Effects of organic modifier type and concentration on chiral separation and quantification of standard solution as well as matrix-ma...detailed

Development of a novel LC–MS/MS method for quantitation of TRITICONAZOLE (cas 131983-72-7) enantiomers in rat plasma and tissues and application to study on toxicokinetics and tissue distribution07/27/2019

Triticonazole with an asymmetrical carbon atom has two enantiomers and is a broad-spectrum systemic fungicide, but its disposition in animals is unclear. In this study, a chiral analytical method of LC–MS/MS was developed and validated for the assay of triticonazole enantiomers in rat plasma an...detailed

131983-72-7Relevant articles and documents

Fungicidal compositions containing (benzylidene)-azolylmethylcycloalkane

-

, (2008/06/13)

(Benzylidene)-azolylmethylcycloalkane or -alkene of formula STR1 in which: A and A1 are hydrocarbon chains of 1 to 3 carbon atoms, R1, R2, R3, R4 and R5 are hydrocarbon radicals, X is halog

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