Trinexapac-ethyl Chemical Properties

Melting point:

32-36°C

Boiling point:

355.44°C (rough estimate)

Density 

1.2380 (rough estimate)

refractive index 

nD30 1.5350

storage temp. 

Sealed in dry,Room Temperature

solubility 

Chloroform (Slightly), Methanol (Slightly)

pka

4.7(at 25℃)

color 

Off-White to Dark Yellow

InChIKey

RVKCCVTVZORVGD-QXMHVHEDSA-N

CAS DataBase Reference

95266-40-3(CAS DataBase Reference)

EPA Substance Registry System

Trinexapac-ethyl (95266-40-3)

Safety Information

WGK Germany 

2

RTECS 

GU8473500

HS Code 

29183000

Toxicity

LD50 in rats (mg/kg): 4460 orally; >4000 dermally (Kerber)

Trinexapac-ethyl Usage And Synthesis

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.

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