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Hydramethylnon

Product Name
Hydramethylnon
CAS No.
67485-29-4
Chemical Name
Hydramethylnon
Synonyms
Hydramethylon;AMDRO;Matox;COMBAT;Wipeout;MAXFORCE;ac217300;cl217300;AC 217300;CL 217300
CBNumber
CB0296517
Molecular Formula
C25H24F6N4
Formula Weight
494.48
MOL File
67485-29-4.mol
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Hydramethylnon Property

Melting point:
185-190°C
Boiling point:
510.5±60.0 °C(Predicted)
Density 
1.2816 (estimate)
vapor pressure 
2.7 x l0-6 Pa (25 °C)
storage temp. 
0-6°C
solubility 
Chloroform (Slightly), DMSO (Sparingly), Methanol (Slightly)
Water Solubility 
0.005-0.007 mg l-1(25 °C)
pka
14.38±0.40(Predicted)
BRN 
6015162
Stability:
Light Sensitive
CAS DataBase Reference
67485-29-4(CAS DataBase Reference)
NIST Chemistry Reference
2(1H)-pyrimidinone, tetrahydro-5,5-dimethyl-, (3-(4-(trifluoromethyl)phenyl)-1-(2-(4-(trifluoromethyl)phenyl)ethenyl)-2-propenylidene)hydrazone(67485-29-4)
EPA Substance Registry System
Hydramethylnon (67485-29-4)
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Safety

Hazard Codes 
T;N,N,T
Risk Statements 
22-36-48/25-50/53
Safety Statements 
1/2-22-26-36/37-45-60-61
RIDADR 
UN3077 9/PG 3
WGK Germany 
3
RTECS 
UW7583000
Hazardous Substances Data
67485-29-4(Hazardous Substances Data)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H302Harmful if swallowed

H319Causes serious eye irritation

H372Causes damage to organs through prolonged or repeated exposure

H410Very toxic to aquatic life with long lasting effects

Precautionary statements

P273Avoid release to the environment.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P314Get medical advice/attention if you feel unwell.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
35373
Product name
Hydramethylnon
Purity
PESTANAL
Packaging
100mg
Price
$225
Updated
2024/03/01
TRC
Product number
H675200
Product name
Hydramethylon
Packaging
250mg
Price
$160
Updated
2021/12/16
Adipogen Life Sciences
Product number
CDX-H0096-M100
Product name
Hydramethylnon
Purity
≥98%(HPLC)
Packaging
100mg
Price
$88
Updated
2021/12/16
Medical Isotopes, Inc.
Product number
40852
Product name
Hydramethylnon
Packaging
250mg
Price
$390
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
PST0000144
Product name
HYDRAMETHYLNON
Purity
95.00%
Packaging
1G
Price
$970.2
Updated
2021/12/16
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Hydramethylnon Chemical Properties,Usage,Production

Description

Hydramethylnon is an organic pesticide active ingredient from the trifluoromethyl aminohydrazone chemical class. It is a registered chemical alternative for chlorpyrifos for use as a termiticide and against ants, crickets, and cockroaches around the home and lawn. Hydramethylnon is also used in a wide variety of professional pesticide products and in various formulations, These include foaming products, granular products, gel baits, liquid concentrates.

Chemical Properties

Yellow to orange crystal, solubility (25°C): water 0.005～0.007mg/L, (20°C) acetone 360g/L, chlorobenzene 390g/L, 1,2-dichloroethane 170g/L, ethanol 72g/L, methanol 230g/L, isopropanol 12g/L, xylene 94g/L. Stable at 25°C for 2 years, stable at 45°C for 90 days, decomposition by sunlight DT50 about 1 hour; fluorantrazone aqueous suspension is stable to hydrolysis, DT50 24-33 days (pH 4.9), 10-11 days (pH 7,03), 11-12 days (pH 8.87). Decomposition of DT50 in soil took about 6 days.

History

Hydramethylnon was developed by DuPont in 1975 and introduced to ornamentals industry in the 1990s. Acequinocyl was also discovered by DuPont in the 1970s and further developed by AgroKanesbo Co. Ltd. and Tomen Agro in Japan. Arysta LifeScience first introduced acequinocyl to the U.S. ornamentals market in 2005. Bifenazate was first developed by Uniroyal Chemical in 1990 and commercialized by Crompton Corporation in 1999. Bifenazate was introduced to the ornamental market in 2010.

Uses

Hydramethylon is an insecticide primarily used in the form of baits for cockroaches and ants.

Definition

ChEBI: Hydramethylnon is a member of the class of hydrazones that is used as an insecticide for control of ants and cockroaches. It has a role as a mitochondrial cytochrome-bc1 complex inhibitor and an insecticide. It is a hydrazone, a member of pyrimidines, a member of (trifluoromethyl)benzenes, an olefinic compound and a member of guanidines.

Preparation

Hydramethylnon synthesis was achieved through the coupling in alcoholic media refluxing the compound 1,5-bis[p-(trifluoromethoxy)phenyl]-1,4-pentadien-3-one afforded the desired product in 50% yield.

Synthesis of hydramethylnon

Application

Hydramethylnon is used in baits for selective control of agricultural and household Formicidae (especially Camponot us, Iridomyrmex, Monomorium, Solenopsis and Pogomyrmex spp. and Pheidole megacephala). It is also used to control Blattellidae (especially Blatta, Blattella, Periplaneta and Supella spp.). It can be carried into the nest by worker ants and kill the queen because it is slow acting.

General Description

Hydramethylnon appears as odorless yellow crystals. Insoluble in water. Used as an insecticide.

Air & Water Reactions

Insoluble in water. Hydrolysis occurs rapidly at low and high pHs.

Reactivity Profile

Hydramethylnon is a trifluoromethyl amidinohydrazone.

Safety Profile

Hydramethylnon is safe to use when applied according to label directions. It has been classified by the EPA as being a low threat when it comes to toxicity to humans, pets and birds.

Metabolic pathway

Amdro (AC 217,300) is rapidly photodegraded under borosilicate-filtered xenon arc lamps at 27 C as a suspension in distilled water. The half-life of amdro is calculated as 42 min and four degradation products are identified as 1,5-bis(a,a,a-trifluoro-p-tolyl)-1,4- pentadien-3-one, a,a,a-trifluoro-p-toluic acid, p- (trifluoromethyl)cinnamic acid, 6,7,8,9-tetrahydro-7,7- dimethyl-3-[p-(trifluoromethyl)styryl]-4H-pyrimido[2,1-c]- as-triazin-4-one. These degradation products are identical to those of the metabolites by insect.

Degradation

Hydramethylnon is relatively involatile and has a very low water solubility for a compound of intermediate lipophilicity. Such a low water solubility may have consequences for the redistribution in the environment and the toxicological properties of the insecticide. Hydramethylnon is rapidly degraded in sunlight by photolysis (DT50 about 1 hour) (PM). Mallipudi et al. (1986) studied the photolytic degradation of a suspension of hydramethylnon in distilled water. Stirred suspensions of [14C-benzylic]- or [2-14C-pyrimidinyl]-hydramethylnwone re exposed to a xenon lamp (filtered to simulate natural sunlight) at 27°C for 60 or 90 minutes. Experiments were done using 1:l mixtures of 14C- and 13C-radiolabelled compounds to aid identification of photoproducts by CI, PI, and NI GC-MS with a pulsed positive-ion negative-ion chemical ionisation accessory. Analysis was also done using a range of TLC and HPLC methods. [14C-benzylic]- and [2-14C-pyrimidinyl]-Hydramethylnon.photo-degraded very rapidly (DT50 41.9 minutes). HPLC analysis showed 16 metabolites from benzylic-labelled and 9 from pyrimidine-labelled material. Identified photoproducts of [14C-benzylic]hydramethylnowne re the pentadienone (2), the benzoic acid (3) and the cinnamic acid (4). In addition, the cyclic derivative (5) was characterised as a photoproduct of both [1 4C-benzyEic]- and [2-14C-pyrimidinyl]-hydramethylnon.Control samples were maintained in the dark for comparison. The photoproducts were of minor importance because they were less abundant than the parent hydramethylnon at all sampling times (HSE, 1994).
Unlabelled hydramethylnon was prepared (presumably as a suspension) in aqueous buffer solutions of pH 4.8,6.5 and 8.0. The suspensions were exposed to sunlight (December, West Bengal, India, average temperatures in the range l0-25 °C) for 10 hours. Solutions of different pH degraded at similar rates (DT50 3.5 hours). In a study done for comparison no significant degradation of hydramethylnon occurred in the dark. In an additional study done to identify photoproducts, a concentrated suspension of hydramethylnon was suspended in aqueous buffer (pH 6.5) and exposed to natural sunlight for 20 hours. The solution was analysed using TLC, GC and column chromatography. The pentadienone (2) was formed by hydrolytic cleavage of hydramethylnon. The resulting hydrazine cleavage product probably underwent self condensation to form the 1,stetrazadiene (6). The condensation may have resulted from the high concentrations used in the study (Chakraborty et al., 1993). A commercial bait formulation of hydramethylnon was spread in trays and placed outdoors (in Florida in June) for up to 4 days. At intervals, samples were taken and analysed by GC. Hydramethylnon was only degraded during daylight hours (DT50 24-30 hours). Products of degradation were not determined (Vander Meer et al., 1982).

Mode of action

Hydramethylnon is a metabolic inhibitor. It works by inhibiting complex III in the mitochondrial inner membrane and leads to a halting of oxidative phosphorylation.

Hydramethylnon Preparation Products And Raw materials

Raw materials

Preparation Products

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Hydramethylnon Suppliers

Canada 1 China 156 France 1 Germany 2 India 1 Japan 1 Switzerland 2 United Kingdom 2 United States 16 Global 182
Pure Chemistry Scientific Inc.
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View Lastest Price from Hydramethylnon manufacturers

Hebei Longbang Technology Co., Ltd
Product
Hydramethylnon 67485-29-4
Price
US $6.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
20TONS
Release date
2024-05-28
HebeiShuoshengImportandExportco.,Ltd
Product
Hydramethylnon 67485-29-4
Price
US $6.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
2000KG/Month
Release date
2024-08-06
Hebei Weibang Biotechnology Co., Ltd
Product
Hydramethylnon 67485-29-4
Price
US $10.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
10 mt
Release date
2024-12-03

67485-29-4, HydramethylnonRelated Search:

ETHANE Dimethyl sulfate Dimethyl ether Dimethyl sulfoxide Dimethicone PHENYL VALERATE N,N-Dimethylaniline Dimethyl sulfone N,N-Dimethylformamide Poly(dimethylsiloxane) Penicillin G sodium salt Dimethyl carbonate Dimethyl fumarate N,N-Dimethylacetamide 4-(TRIFLUOROMETHYL)STYRENE Phenylacetic acid Pyrimidine Hydramethylnon

  • TETRAHYDRO-5,5-DIMETHYL-2(1H)-PYRIMIDINONE [3-[4-(TRIFLUOROMETHYL)-PHENYL]-1-[2-[4-(TRIFLUOROMETHYL)-PHENYL]ETHENYL]-2-PROPENYLIDENE]-HYDRAZONE
  • Tetrahydro-5,5-dimethyl-2(1H)-pyrimidinone[3-[4-(trifluoromethyl)phenyl]-1-[2-[4-(trifluoromethyl)phenyl]ethenyl]-2-propenylidene]hydrazone
  • AC 217300(R)
  • AMDRO
  • Wipeout
  • hydramrthynon
  • AMDRO, 100MG, NEAT
  • Hydramethylon
  • 2(1H)-Pyrimidinone, tetrahydro-5,5-dimethyl-, 3-4-(trifluoromethyl)phenyl-1-2-4-(trifluoromethyl)phenylethenyl-2-propenylidenehydrazone
  • (TETRAHYDRO-5,5-DIMETHYL-2(1H)-PYRIMIDINONE)(1,5-BIS(A,A,.
  • 5-dimethyl-tetrahydro-(3-(4-(trifluoromethyl)phenyl)-1-2(1h)-pyrimidinon(2-(4- (trifluoromethyl)phenyl)ethenyl)-2-propenylidene)hydrazone
  • 5,5-dimethyl-perhydro-pyrimidin-2-one α-(4-trifluoromethylstyryl)-α-(4-trifluoromethyl)cinnamylidenehydrazone
  • TETRAHYDRO-5,5-DIMETHYL-2(1H)-PYRIMIDINONE[p-(TRIFLUOROMETHYL)-ALPHA-[p-(TRIFLUOROMETHYL)STYRYL]CINNAMYLIDENE]HYDRAZONE
  • TETRAHYDRO-5,5-DIMETHYL-2(1H)-PYRIMIDINONE(3-(4-TRIFLUOROMETHYL)PHENYL)-1-(2-(4-TRIFLUOROMETHYL)PHEN
  • 2-{2-[(1E,4E)-1,5-bis[4-(trifluoroMethyl)phenyl]penta-1,4-dien-3-ylidene]hydrazin-1-ylidene}-5,5-diMethyl-1,3-diazinane
  • 1,5-Bis[4-(trifluoromethyl)phenyl]-1,4-pentadien-3-one 2-(1,4,5,6-tetrahydro-5,5-dimethyl-2-pyrimidinyl)hydrazone
  • NSC 379665
  • Tetrahydro-5,5-dimethyl-2(1H)-pyrimidinone[3-[4-(trifluoromethyl)phenyl]-1-[2-[4-(trifluoromethyl)phenyl]ethenyl]-2-propylidene]hydrazone
  • (E,E)-hydramethylnon
  • Hydramethylnon Standard
  • MAXFORCE
  • HYDRAMETHYLNON
  • HYDRAMETHYLNONE
  • COMBAT
  • (1E,4E)-1,5-Bis[4-(trifluoromethyl)phenyl]-1,4-pentadien-3-one (5,5-dimethyltetrahydro-2(1H)-pyrimidinylidene)hydrazone
  • (2-(4-(trifluoromethyl)phenyl)ethenyl)-2-propenylidene)hydrazone
  • 2(1H)-Pyrimidinone,tetrahydro-5,5-dimethyl-,[3-[4-(trifluoromethyl)phenyl]-1-[2-[4-(trifluoromethyl)phenyl]ethenyl]-2-propenylidene]hydrazone
  • 5-dimethyl-tetrahydro-(3-(4-(trifluoromethyl)phenyl)-1-2(1h)-pyrimidinon
  • AC 217300
  • ac217300
  • CL 217300
  • cl217300
  • Matox
  • tetrahydro-5,5-dimethyl-2(1h)-pyrimidinon(3-(4-(trifluoromethyl)phenyl)-1-(2-(4-(trifluoromethyl)phenyl)ethenyl)-2-propenylidene)hydrazone
  • Hydramethylnon @100 μg/mL in MeOH
  • 1,4-Pentadien-3-one, 1,5-bis[4-(trifluoromethyl)phenyl]-, 2-(1,4,5,6-tetrahydro-5,5-dimethyl-2-pyrimidinyl)hydrazone
  • Hydramethylnon Solution in Methanol, 1000μg/mL
  • Hydramethylnon 67485-29-4
  • Hydromethylnon
  • C14220000 Hydramethylnon
  • Hydramethylnon in Methanol
  • Sofosbuvir Impurity 144
  • 67485-29-4
  • C25H24F6N4
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