ChemicalBook > CAS DataBase List > RESMETHRIN

RESMETHRIN

Product Name
RESMETHRIN
CAS No.
10453-86-8
Chemical Name
RESMETHRIN
Synonyms
Seco;ari-b;Syntox;xylate;For-syn;Vectrin;CHRYSON;Scourge;OMS-1206;Premgard
CBNumber
CB9311222
Molecular Formula
C22H26O3
Formula Weight
338.44
MOL File
10453-86-8.mol
More
Less

RESMETHRIN Property

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
EPA Substance Registry System
Resmethrin (10453-86-8)
More
Less

Safety

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
Hazardous Substances Data
10453-86-8(Hazardous Substances Data)
Toxicity
LC50 (96 hr) in rainbow trout, bluegill sunfish (mg/l): 3.14, 7.2 (Rand)
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H410Very toxic to aquatic life with long lasting effects

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P273Avoid release to the environment.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P391Collect spillage. Hazardous to the aquatic environment

P501Dispose of contents/container to..…

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
45655
Product name
Resmethrin
Purity
PESTANAL
Packaging
250mg
Price
$94.5
Updated
2024/03/01
Usbiological
Product number
465998
Product name
seco-
Packaging
100mg
Price
$460
Updated
2021/12/16
Usbiological
Product number
465997
Product name
seco-
Packaging
1mg
Price
$489
Updated
2021/12/16
TRC
Product number
R144685
Product name
Resmethrin
Packaging
500mg
Price
$790
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
PST0000294
Product name
RESMETHRIN
Purity
95.00%
Packaging
5MG
Price
$495.96
Updated
2021/12/16
More
Less

RESMETHRIN Chemical Properties,Usage,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

More
Less

RESMETHRIN Suppliers

Canada 1 China 71 Europe 1 France 2 Germany 2 India 2 Japan 2 Switzerland 2 United Kingdom 3 United States 21 Global 107
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
BEST-REAGENT
Tel
400-1166-196 18981987031
Fax
028-84555506 800101999
Email
cdhxsj@163.com
Country
China
ProdList
11726
Advantage
57
Chengdu Ai Keda Chemical Technology Co., Ltd.
Tel
4008-755-333 18080918076
Fax
028-86757656
Email
800078821@qq.com
Country
China
ProdList
9725
Advantage
55
Nanjing Sunlida Biological Technology Co., Ltd.
Tel
025-57798810
Fax
025-57019371
Email
sales@sunlidabio.com
Country
China
ProdList
3750
Advantage
55
Shanghai JONLN Reagent Co., Ltd.
Tel
400-0066400 13621662912
Fax
021-55660885
Email
422131432@qq.com
Country
China
ProdList
9986
Advantage
55
TianJin Alta Scientific Co., Ltd.
Tel
022-65378550-8551
Fax
+86-022-2532-9655
Email
contact@altascientific.com
Country
China
ProdList
2773
Advantage
58
Alta Scientific Co., Ltd.
Tel
022-6537-8550 15522853686
Fax
022-2532-9655
Email
sales@altasci.com.cn
Country
China
ProdList
4515
Advantage
55
Shanghai EFE Biological Technology Co., Ltd.
Tel
021-65675885 18964387627
Fax
021-65675885
Email
info@efebio.com
Country
China
ProdList
9709
Advantage
58
Raw material medicin reagent co.,Ltd
Tel
025-57798860
Email
sales@njromanme.com
Country
China
ProdList
4534
Advantage
58
Shandong Ono Chemical Co., Ltd.
Tel
0539-6362799 20）
Fax
0539-6362799（To 20）
Country
China
ProdList
9998
Advantage
58
Shenzhen Regent Biochemical Technology Co., Ltd.
Tel
0755-0755-85201366 18938635012
Fax
0755-85201366
Email
sales@regentsciences.com
Country
China
ProdList
9293
Advantage
58
Shanghai Jizhi Biochemical Technology Co. Ltd.
Tel
400-400-400-9004166 18616739031
Email
3007523370@qq.com
Country
China
ProdList
52712
Advantage
58
Beijing altar ink quality inspection technology co., LTD
Tel
010-52889049
Email
2250970673@qq.com
Country
CHINA
ProdList
1133
Advantage
58
Shenzhen Polymeri Biochemical Technology Co., Ltd.
Tel
+86-400-002-6226 13028896684
Email
sales@rrkchem.com
Country
China
ProdList
55827
Advantage
58
Hebei Yanxi Chemical Co., Ltd.
Tel
+8617531190177
Email
peter@yan-xi.com
Country
China
ProdList
5993
Advantage
58
Hefei TNJ Chemical Industry Co.,Ltd.
Tel
0551-65418671
Fax
0551-65418697
Email
sales@tnjchem.com
Country
China
ProdList
34572
Advantage
58
Hubei Ipure Biology Co., Ltd
Tel
+8613367258412
Fax
18062427325
Email
ada@ipurechemical.com
Country
China
ProdList
10326
Advantage
58
Hebei Mojin Biotechnology Co., Ltd
Tel
+8613288715578
Email
sales@hbmojin.com
Country
China
ProdList
12456
Advantage
58
AFINE CHEMICALS LIMITED
Tel
0571-85134551
Fax
008657185134895
Email
info@afinechem.com
Country
CHINA
ProdList
15377
Advantage
58
Hubei Jusheng Technology Co.,Ltd.
Tel
18871490254
Fax
027-59599243
Email
linda@hubeijusheng.com
Country
CHINA
ProdList
28180
Advantage
58
Xibao Biotechnology (Shanghai) Co., Ltd.
Tel
13761246140
Email
58642714@qq.com
Country
China
ProdList
415
Advantage
58
Chongqing Chemdad Co., Ltd
Tel
+86-023-61398051 +8613650506873
Email
sales@chemdad.com
Country
China
ProdList
39916
Advantage
58
Shaanxi Dideu Medichem Co. Ltd
Tel
+86-29-87569266 15319487004
Fax
029-88380327
Email
1015@dideu.com
Country
China
ProdList
2263
Advantage
58
ShangHai Anpel Co, Ltd.
Tel
18501792038; 18501792038
Email
shanpel@anpel.com.cn
Country
China
ProdList
9614
Advantage
58
Shanghai Haohong Pharmaceutical Co., Ltd.
Tel
400-400-8210725 4008210725
Email
malulu@leyan.com
Country
China
ProdList
55023
Advantage
58
Hebei mo Jin biotechnology co., ltd
Tel
13288715578
Email
angelia@hbmojin.com
Country
China
ProdList
1759
Advantage
58
Shandong Nayazuo Chemical Technology Co. LTD
Tel
400-873-6778 18660992876
Fax
0539-6267369
Email
3584419101@qq.com
Country
China
ProdList
4975
Advantage
58
Energy Chemical
Tel
021-58432009 400-005-6266
Fax
021-58436166
Email
marketing1@energy-chemical.com
Country
China
ProdList
44894
Advantage
58
Wuhan Yanzhe Technology Co., Ltd
Tel
15527250409
Fax
QQ：2692360204
Email
wenhaotian12@163.com
Country
China
ProdList
4576
Advantage
58
Changzhou Furuisi Biotechnology Co., Ltd
Tel
0519-85524369
Email
3477467573@qq.com
Country
China
ProdList
8618
Advantage
58
Hubei Xinkang Pharmaceutical Chemical Co., Ltd
Tel
027-027-59308705 18871579363
Fax
027-59308705
Email
1248680011@qq.com
Country
China
ProdList
9984
Advantage
58
Hubei Shishun Biotechnology Co. Ltd
Tel
027-59223025 15107168801
Fax
027-59223025
Email
1718480011@qq.com
Country
China
ProdList
9990
Advantage
58
Tianmen Hengchang Chemical Co., Ltd
Tel
027-59322316 15172518801
Fax
027-59322316
Email
1208480077@qq.com
Country
China
ProdList
9944
Advantage
58
Hubei Qifei Pharmaceutical Chemical Co., Ltd
Tel
027-027-59322506 18071128681
Fax
027-59322506
Email
1438082200@qq.com
Country
China
ProdList
9995
Advantage
58
Hebei mo Jin biotechnology co., ltd
Tel
15097329902
Fax
18503279000
Email
sales@hebeimojin.com
Country
China
ProdList
2254
Advantage
58
TCI (Shanghai) Chemical Trading Co., Ltd.
Tel
021-61109150
Fax
021-61105897
Email
sales@tcisct.com
Country
China
ProdList
31163
Advantage
58
Hebei Momojin Biological Technology Co., Ltd
Tel
13315457394 13315457394
Email
june@hbmojin.com
Country
China
ProdList
2689
Advantage
58
Shanghai Chemisci Technology Co., Ltd
Tel
021-58690851 15690882017
Email
1877080091@qq.com
Country
China
ProdList
7992
Advantage
58
Hubei Weideli Chemical Reagent Co.，Ltd.
Tel
13339985473
Email
C13339985473@163.com
Country
China
ProdList
3460
Advantage
58
Shaanxi Dideu Newmaterial Co., Ltd.
Tel
029-63373950 15353716720
Email
1052@dideu.com
Country
China
ProdList
10008
Advantage
58
Hubei Wanye Zhongcheng Chemical Reagent Co., Ltd.
Tel
18671296875
Email
1205035102@qq.com
Country
China
ProdList
4070
Advantage
58
Hangzhou Yaoruiyicheng Biological Medicine Co., Ltd
Tel
18072846723
Email
caigou1@witofly.com
Country
China
ProdList
18926
Advantage
58
Aobolihui
Tel
0917-18691729 18691729963
Email
2553382659@qq.com
Country
China
ProdList
4758
Advantage
58
Shanghai Bikai Technology Co. , Ltd.
Tel
18516304666
Email
christina.feng@cpachem-sh.com
Country
China
ProdList
3101
Advantage
58
Shandong Mopai Biotechnology Co., Ltd
Tel
13053322091 13053322091
Email
admin@mopaikeji.com
Country
China
ProdList
10969
Advantage
58
Nantong Zhonghe Chemical New Materials Co., Ltd
Tel
13003551299 13003551299
Email
2369399482@qq.com
Country
China
ProdList
7568
Advantage
58
Hubei Shiteng Chemical Technology Co. LTD
Tel
189-71850150 19086915685
Email
1273131441@qq.com
Country
China
ProdList
4998
Advantage
58
guoyungurui
Tel
18162595016
Email
3287908757@qq.com
Country
China
ProdList
10016
Advantage
58
Xi'an Lechun Chemical Co., Ltd
Tel
029-15596886083 15596886083
Email
739383595@qq.com
Country
China
ProdList
3449
Advantage
58
Shanghai Acmec Biochemical Technology Co., Ltd.
Tel
+undefined18621343501
Email
product@acmec-e.com
Country
China
ProdList
33349
Advantage
58
More
Less

View Lastest Price from RESMETHRIN manufacturers

Hebei Duling International Trade Co. LTD
Product
RESMETHRIN 10453-86-8
Price
US $50.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
20 tons
Release date
2023-03-24
Hebei Yanxi Chemical Co., Ltd.
Product
RESMETHRIN 10453-86-8
Price
US $0.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
20tons
Release date
2023-09-19
Hebei Mojin Biotechnology Co., Ltd
Product
RESMETHRIN 10453-86-8
Price
US $0.00/ASSAYS
Min. Order
1ASSAYS
Purity
99%
Supply Ability
20tons
Release date
2021-07-08

10453-86-8, RESMETHRINRelated Search:

ETHYL TERT-BUTYLACETATE RESMETHRIN 3-FURANMETHANOL VINYLCYCLOPROPANE 2-METHYLCYCLOPROPANECARBOXYLIC ACID Ethyl cyclopropanecarboxylate Methyl cyclopropane carboxylate 2-Ethylfuran 2,2-DIMETHYL-3-(2-METHYLPROP-1-ENYL)CYCLOPROPANECARBOXYLIC ACID 2,2-DIMETHYL CYCLOPROPYL CARBOXYLIC ACID CHRYSANTHEMYL ALCOHOL METHYL TERT-BUTYLACETATE 3,3-Dimethylbutyric acid d-trans-resmethrin (esa),(1r)-trans-resmethri Ethyl 2-methyl-4-pentenoate Ethyl chrysanthemumate Cyclopropanecarboxylic acid RESMETHRIN ALCOHOL METABOLITE

  • (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
  • 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
  • Ethyl 3-Oxo-4-aza-5&alpha
  • (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