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RESMETHRIN

CAS No.
10453-86-8
Chemical Name:
RESMETHRIN
Synonyms
Seco;ari-b;Syntox;xylate;Vectrin;CHRYSON;For-syn;Scourge;Premgard;SBP 1382
CBNumber:
CB9311222
Molecular Formula:
C22H26O3
Molecular Weight:
338.44
MDL Number:
MFCD00041806
MOL File:
10453-86-8.mol
MSDS File:
SDS
Last updated:2023-09-20 08:34:21

RESMETHRIN Properties

Melting point 56.5℃
Boiling point bp >180° (dec)
Density 0.96 g/cm3
vapor pressure ﹤l×10-5 Pa (25 °C)
refractive index 1.5287 (20℃)
Flash point closed cup: 264.2°F (129°C)
storage temp. 0-6°C
solubility Chloroform (Slightly), Methanol (Slightly, Heated)
Water Solubility 0.038 mg l-1 (25 °C)
BRN 1626510
EWG's Food Scores 5
FDA UNII Z6PN6KTG4K
Proposition 65 List Resmethrin
NCI Drug Dictionary Vectrin
EPA Substance Registry System Resmethrin (10453-86-8)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS07,GHS09
Signal word  Warning
Hazard statements  H302-H410
Precautionary statements  P264-P270-P273-P301+P312-P391-P501
Hazard Codes  Xn,N
Risk Statements  22-50/53
Safety Statements  60/61-61-60
RIDADR  3082
WGK Germany  3
RTECS  GZ1310000
HazardClass  9
PackingGroup  III
HS Code  29321900
Toxicity LC50 (96 hr) in rainbow trout, bluegill sunfish (mg/l): 3.14, 7.2 (Rand)

RESMETHRIN price More Price(6)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 45655 Resmethrin PESTANAL 10453-86-8 250mg $94.5 2024-03-01 Buy
Usbiological 465998 seco- 10453-86-8 100mg $460 2021-12-16 Buy
Usbiological 465997 seco- 10453-86-8 1mg $489 2021-12-16 Buy
TRC R144685 Resmethrin 10453-86-8 500mg $790 2021-12-16 Buy
American Custom Chemicals Corporation PST0000294 RESMETHRIN 95.00% 10453-86-8 5MG $495.96 2021-12-16 Buy
Product number Packaging Price Buy
45655 250mg $94.5 Buy
465998 100mg $460 Buy
465997 1mg $489 Buy
R144685 500mg $790 Buy
PST0000294 5MG $495.96 Buy

RESMETHRIN Chemical Properties,Uses,Production

Chemical Properties

Off-white to tan waxy solid or colorless crys- tals. Chrysanthemum-like odor. Commercial products may be dissolved in flammable organic solvents

Uses

Resmethrin is used to control a wide range of insects in horticultural, household, public health and animal health situations. It has some agricultural use but this is limited. The more active 1Rtrans form has a similar range of uses and is also used in stored grain products.

Definition

ChEBI: Resmethrin is a member of furans and a cyclopropanecarboxylate ester. It has a role as a pyrethroid ester insecticide and an agrochemical. It is functionally related to a chrysanthemic acid.

General Description

Colorless crystals or waxy solid. Insoluble in water. Used as an insecticide.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

A pyrethroid derivative.

Agricultural Uses

Insecticide: Resmethrin is currently used for mosquito control (by aerial application) in the USA, and may can also be used in greenhoused to control white fly. Resmethrin is a synthetic Type I pyrethroid insecticide registered for control of insects in residential, commercial and industrial settings, and in animal living areas. Resmethrin is also registered for use in food-handling establishments and as a restricted use pesticide when used in ULV spray to control adult mosquitoes in the interest of public health[83]. Restricted Use Pesticide (RUP) when formulated for use in mosquito abatement and pest control treatments at nonagricultural sites. Restricted due to extreme fish toxicity. Not approved for use in EU countries.

Trade name

(d-trans-isomer); SBP® 1382 (d-trans-isomer); d-transSBP® 1382 (d-trans-isomer); SBP®-1390; S. B. PENICK 1382®; SCOURGE®; SUN-BUGGER®; SYNTHRIN®; SYNTOX®; VECTRIN®; WHITMIRE® PT-110

Safety Profile

Poison by ingestion, andintravenous routes. Moderately toxic by inhalation andskin contact. When heated to decomposition it emits acridand irritating fumes.

Potential Exposure

Resmethrin is pyrethroid insecticide used for mosquito control (by aerial application) in the USA, and may can also be used in greenhouses to control white fly. Resmethrin is a synthetic Type I pyrethroid insecticide registered for control of insects in residential, commercial, and industrial settings, and in animal living areas. It is also registered for use in food handling estab- lishments and as a restricted use pesticide when used in ULV spray to control adult mosquitoes in the interest of public health . A United States Restricted Use Pesticide (RUP) when formulated for use in mosquito abatement and pest control treatments at nonagricultural sites. Restricted due to extreme fish toxicity.

Metabolic pathway

14C-resmethrin are individually administered orally to white leghorn hens, and more than 90% of the radioactivity is eliminated in the excreta within 24 h of treatment. The metabolic routes for both resmethrin isomers arise from ester hydrolysis and oxidation of the hydrolytic products. Some of these metabolites are further conjugated with glucuronic acid, sulfate, or other unidentified compounds before excretion.

Shipping

UN3352 Pyrethroid pesticide, liquid toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials. UN3349 Pyrethroid pesticide, solid toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous material

Degradation

The resmethrins are reasonably stable but they are sensitive to base hydrolysis forming the chrysanthemic acid isomers (2) and 5-benzyl-3- furylmethanol (3). They are also sensitive to oxidation and to photodecomposition. Photo-oxidation involves degradation of the furan ring to yield a cyclic ozonide peroxide by addition of oxygen across the unsaturated system forming the hydroxylactone derivative (4), the benzyloxylactone derivative (5) and the hydroxycyclopentenolone (6) (Ueda et al., 1974). These chemical and photochemical reactions are shown in Scheme 1.
Degradation also occurs in the acid moiety by reactions analogous to those described under phenothrin, for example, oxidation at the isobutylene substituent to afford a variety of alcohols, aldehydes and carboxylic acids. These two sites of weakness in the resmethrin molecule result in considerable photo-instability (though they are more stable than the pyrethrins) and to a complex mixture of degradation products.

Incompatibilities

Decomposed by air, light, alkaline media, and temperatures .175℃. May react violently with strong oxidizers, bromine, 90% hydrogen peroxide, phos- phorus trichloride, silver powders or dust. Incompatible with silver compounds. Mixture with some silver compounds forms explosive salts of silver oxalate.

Waste Disposal

Incineration would be an effective disposal procedure where permitted. If an efficient incinerator is not available, the product should be mixed with large amounts of combustible material and contact with the smoke should be avoided. In accordance with 40CFR165. Follow recommendations for the disposal of pesticides and pesticide containers . Bury in noncrop land away from water. It would be better to mix the prod- uct with lime. Incineration would be an effective disposal procedure where permitted. If an efficient incinerator is not available, the product should be mixed with large amount of combustible material. Recommendable methods: Hydrolysis, landfill, incineration, and open burning. Not recommendable method: Discharge to sewer. Mix with saw- dust and burn at a remote place .

RESMETHRIN Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 107)Suppliers
Supplier Tel Email Country ProdList Advantage
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28180 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873 sales@chemdad.com China 39916 58
Shaanxi Dideu Medichem Co. Ltd
+86-29-87569266 15319487004 1015@dideu.com China 2263 58
Hebei Mojin Biotechnology Co., Ltd
+8613288715578 sales@hbmojin.com China 12456 58
Hebei Yanxi Chemical Co., Ltd.
+8617531190177 peter@yan-xi.com China 5993 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Hubei Ipure Biology Co., Ltd
+8613367258412 ada@ipurechemical.com China 10326 58
Hefei TNJ Chemical Industry Co.,Ltd.
0551-65418671 sales@tnjchem.com China 34572 58
AFINE CHEMICALS LIMITED
0571-85134551 info@afinechem.com CHINA 15377 58
Shaanxi Didu New Materials Co. Ltd
+86-89586680 +86-13289823923 1026@dideu.com China 9116 58

View Lastest Price from RESMETHRIN manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
RESMETHRIN pictures 2023-09-19 RESMETHRIN
10453-86-8
US $0.00 / kg 1kg 99% 20tons Hebei Yanxi Chemical Co., Ltd.
RESMETHRIN pictures 2023-03-25 RESMETHRIN
10453-86-8
US $50.00 / kg 1kg 99% 20 tons Hebei Duling International Trade Co. LTD
RESMETHRIN pictures 2023-01-31 RESMETHRIN
10453-86-8
US $0.00 / ASSAYS 1ASSAYS 99% 20tons Hebei Mojin Biotechnology Co., Ltd
  • RESMETHRIN pictures
  • RESMETHRIN
    10453-86-8
  • US $0.00 / kg
  • 99%
  • Hebei Yanxi Chemical Co., Ltd.
  • RESMETHRIN pictures
  • RESMETHRIN
    10453-86-8
  • US $50.00 / kg
  • 99%
  • Hebei Duling International Trade Co. LTD
  • RESMETHRIN pictures
  • RESMETHRIN
    10453-86-8
  • US $0.00 / ASSAYS
  • 99%
  • Hebei Mojin Biotechnology Co., Ltd
opanecarboxylate Penick 1382 Penick SBP 1382 penick1382 penncapthrin Premgard Sun-Bugger Sun-Bugger 4 Syntox uryl)methylester Vectrin Whitmire PT-110 xylate FMC 17370 CHRYSRON(R) CHRYSON BENZOFUROLINE SBP 1382 SYNTHRIN SYNTHRIN(R) RESMETHRIN NIA 17370 NRDC 104 5-BENZOYL-3-FURYLMETHYL (1RS)-CIS-TRANS-CHRYSANTHEMATE 5-BENZYL-3-FURYLMETHYL (1R,S)-CIS,TRANS-CHRYSANTHEMATE (5-BENZYL-3-FURYL)METHYL-2,2-DIMETHYL-3-(2-METHYLPROPENYL) CYCLOPROPANECARBOXYLATE (5-BENZYL-3-FURYL)METHYL-2,2-DIMETHYL-3-(2-METHYLPROPHENYL) CYCLOPROPANECARBOXYLATE RESMETHRIN, 250MG, NEAT RESMETHRIN PESTANAL, 250 MG 2,2-Dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylic acid [5-(phenylmethyl)-3-furanyl]methyl ester Resmethrinl (5-(phenylmethyl)-3-furanyl)methyl2,2-dimethyl-3-(2-methyl-1-propenyl)cyclop ethyl)-3-furanyl]methylester For-syn lopropanecarboxylate -methylpropenyl)cyclopropanecarboxylate NSC 195022 nsc195022 OMS-1206 (5-(phenylmethyl)-3-furanyl)methyl2,2-dimethyl-3-furylmethyl2,2-dimethyl-3-(2 (5-(phenylmethyl)-3-furanyl)methylester (5-Benzyl-3-furyl)methyl 2,2-dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylate (5-Benzyl-3-furyl)methyl chrysanthemate (5-benzyl-3-furyl)methyl(1rs)-cis,trans-2,2-dimethyl-3-(2-methylpropenyl)cyc (5-benzyl-3-furyl)methyl-2,2-dimethyl-3-(2-methylpropenyl)-cyclopropanecarbo (5-benzyl-3-furyl)methyl-2,2-dimethyl-3-(2-methylpropenyl)-cyclopropanecarboxy (5-benzyl-3-furyl)methylchrysanthemate (5-phenylmethyl)-3-furanyl)methyl2,2-dimethyl-3-(2-methyl-1-propenyl)cyclopr [5-phenylmethyl-3-furan]methyl-2,2-dimethyl-3-(2-methyl-1-propenyl)cyclopropane 1rs,3rs)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate 1S, cis-Resmethrin 2,2-dimethyl-3-(2-methyl-1-propenyl)-cyclopropanecarboxylicaci[5-(phenylm 2,2-dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylicacid 2,2-Dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylicacid[5-(phenylmethyl)-3-furanyl]methylester 2,2-dimethyl-3-(2-methylpropenyl)cyclopropanecarboxylate 2,2-dimethyl-3-(2-methylpropenyl)-cyclopropanecarboxylicaci(4-(2-benzyl)f 2,2-dimethyl-3-(2-methylpropenyl)-cyclopropanecarboxylicaci(5-benzyl-3-fu 2,2-dimethyl-3-(2-methylpropenyl)cyclopropanecarboxylicacid,(5-benzyl-3-fury