HALOFENOZIDE

Modify Date: 2024-01-04 17:38:37

HALOFENOZIDE Structure
HALOFENOZIDE structure
Common Name HALOFENOZIDE
CAS Number 112226-61-6 Molecular Weight 330.81
Density 1.205g/cm3 Boiling Point N/A
Molecular Formula C18H19ClN2O2 Melting Point 198.0-199.0°
MSDS Chinese USA Flash Point N/A
Symbol GHS07 GHS09
GHS07, GHS09
Signal Word Warning

 Use of HALOFENOZIDE


Halofenozide (RH-0345) is an ecdysteroid agonist. RH-0345 belongs to a new group of insect growth regulators (IGRs) with a benzoylhydrazine structure that mimic the action of the natural insect molting hormone 20-hydroxyecdysone[1].

 Names

Name halofenozide
Synonym More Synonyms

 HALOFENOZIDE Biological Activity

Description Halofenozide (RH-0345) is an ecdysteroid agonist. RH-0345 belongs to a new group of insect growth regulators (IGRs) with a benzoylhydrazine structure that mimic the action of the natural insect molting hormone 20-hydroxyecdysone[1].
Related Catalog
In Vitro Halofenozide (RH-0345) reduces both growth and development of oocytes in vitro[1]. Cell Viability Assay[2] Cell Line: Cultured ovaries were dissected from female adult beetles of mealworm, Tenebrio molitor (T. molitor) Concentration: 1 μM and 10 μM Incubation Time: 4 days Result: Did not cause a significant effect on ecdysteroid amounts in the culture medium using ovaries from 0- and 2-day-old females at 10 μM. Caused a small significant increase of the amounts of ovarian ecdysteroids in the culture medium at 1 μM in the culture medium and with 2-day-old ovaries.
In Vivo After topical application of Halofenozide (RH-0345; 5 and 10 μg) on adult females, the highest dose (10 μg) reduces significantly the reproductive parameters scored: namely the oviposition period, the fecundity and the egg viability[1]. Halofenozide at the two doses tested (5 and 10 μg) causes smaller eggs with a decrease in length, width and volume[1]. Animal Model: Newly emerged (0-day-old) adult females of T. molitor [1] Dosage: 5 and 10 μg Administration: Topically applied Result: Caused smaller eggs with a decrease in length, width and volume at the two doses tested (5 and 10 μg) .
References

[1]. Faïza Taïbi, et al. Effect of ecdysone agonist RH-0345 on reproduction of mealworm, Tenebrio molitor. Comp Biochem Physiol C Toxicol Pharmacol. 2003 Jul;135C(3):257-67.

 Chemical & Physical Properties

Density 1.205g/cm3
Melting Point 198.0-199.0°
Molecular Formula C18H19ClN2O2
Molecular Weight 330.81
Exact Mass 330.11400
PSA 49.41000
LogP 4.31660
Index of Refraction 1.584

 Safety Information

Symbol GHS07 GHS09
GHS07, GHS09
Signal Word Warning
Hazard Statements H317-H411
Precautionary Statements P273-P280
Hazard Codes Xi,N
Risk Phrases 43-51/53
Safety Phrases 24-37-61
RIDADR UN 3077
RTECS DG4976795
Packaging Group III
Hazard Class 9

 Synthetic Route

~%

HALOFENOZIDE Structure

HALOFENOZIDE

CAS#:112226-61-6

Literature: EP982292 A2, ;

 Precursor & DownStream

Precursor  2

DownStream  0

 Articles1

More Articles
Two Leptinotarsa uridine diphosphate N-acetylglucosamine pyrophosphorylases are specialized for chitin synthesis in larval epidermal cuticle and midgut peritrophic matrix.

Insect Biochem. Mol. Biol. 68 , 12-Jan, (2016)

Uridine diphosphate-N-acetylglucosamine-pyrophosphorylase (UAP) is involved in the biosynthesis of chitin, an essential component of the epidermal cuticle and midgut peritrophic matrix (PM) in insects...

 Synonyms

RH 0345
N-tert-butyl-N’-(4-chlorobenzoyl)benzohydrazide
N-tert-Butyl-N'-(4-chlorobenzoyl)benzohydrazide
N'-benzoyl-N'-tert-butyl-4-chlorobenzohydrazide
4-chlorobenzoic acid 2-benzoyl-2-(1,1-dimethylethyl)hydrazide
Mach 2
Halofenozide
N’-benzoyl-N’-tert-butyl-4-chlorobenzohydrazide