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95266-40-3

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95266-40-3 Usage

Description

Trinexapac-ethyl is a synthetic plant growth regulator developed by Syngenta, Switzerland. It inhibits the production of gibberellic acid and shortens the internodes on grasses grown for seed and cereals which results in a reduction in lodging. It can be used for crop height reduction, lodging prevention and yield protection in all varieties of winter and spring wheat, winter and spring barley and winter and spring oats, durum wheat, rye, triticale and grassland (seed crops).

Uses

Trinexapac-ethyl is a synthetic plant growth regulator that is derived from cyclohexanecarboxylate. It is used to control the growth on various grass species and crops. Trinexapac-ethyl is approved for use on cereal crops such as barley, durum wheat, oats, rye, triticale and wheat as well as grassland, amenity turf and managed turf.

Definition

ChEBI: Trinexapac-ethyl is an ethyl ester resulting from the formal condensation of the carboxy group of trinexapac with ethanol. It has a role as a xenobiotic, an environmental contaminant, a plant growth regulator, an agrochemical, a pro-agent and a gibberellin biosynthesis inhibitor. It is a member of cyclohexanones, a beta-hydroxy ketone, an enol, an ethyl ester and a member of cyclopropanes. It derives from a trinexapac.

Carcinogenicity

The U.S. EPA has classified trinexapac-ethyl as "not likely to be carcinogenic to humans."No studies area available in humans to inform on carcinogenicity of trinexapac-ethyl.The carcinogenic potential of trinexapac-ethyl has been well investigated in two guideline and GLP compliant dietary studies; a 2-year study in the Sprague-Dawley rat (Anon., 1992) and an 18-month study in the CD-1 mouse (Anon., 1991).Overall, RAC agreed with the DS that there is insufficient evidence to support classification for carcinogenicity.

Mode of action

Trinexapac-ethyl acts as an inhibitor of the action of a key enzyme in the formation of gibberellic acid (GA1), preventing the formation of the plant growth regulator gibberellins, which promotes cell elongation. In the absence of gibberellins the internodes of the plants fail to grow and prevent the plant from growing taller. This can be used to prevent lodging in crops and amenity turf, increase the yield in crops by redirecting energy into the production of reproductive parts and finally to reduce the frequency of mowing in turf.

Check Digit Verification of cas no

The CAS Registry Mumber 95266-40-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,2,6 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 95266-40:
(7*9)+(6*5)+(5*2)+(4*6)+(3*6)+(2*4)+(1*0)=153
153 % 10 = 3
So 95266-40-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H16O5/c1-2-18-13(17)8-5-9(14)11(10(15)6-8)12(16)7-3-4-7/h7-8,16H,2-6H2,1H3/b12-11-

95266-40-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name trinexapac-ethyl

1.2 Other means of identification

Product number -
Other names Moddus

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:95266-40-3 SDS

95266-40-3Downstream Products

95266-40-3Relevant articles and documents

Production method of 4-cyclopropyl (hydroxy) methylene -3,5-diketone ethyl cyclohexane carboxylate and recycling method thereof

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Paragraph 0142-0146; 0161-0165; 0173-0177, (2019/06/07)

The invention relates to the field of the organic synthesis, and discloses a production method of 4-cyclopropyl (hydroxy) methylene -3,5-diketone ethyl cyclohexane carboxylate and a recycling method thereof. The recycling method comprises the following st

Cyclohexanedionecarboxylic acid derivatives with herbicidal and plant growth regulating properties

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, (2008/06/13)

Novel cyclohexanedionecarboxylic acid derivatives have herbicidal and plant growth regulating properties. The cyclohexanedionecarboxylic acid derivatives have the formula I STR1 wherein A is an --OR2 or --NR3 R4 radical, B

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