Fenitrothion

ChemicalBook > CAS DataBase List > Fenitrothion

Description History Toxicity Effects

Product Name: Fenitrothion
CAS No.: 122-14-5
Chemical Name: Fenitrothion
Synonyms: MEP;Dybar;Fenitrotion;Cyten;oms43;s112a;s5660;Cyfen;cytel;8057hc
CBNumber: CB5406210
Molecular Formula: C9H12NO5PS
Formula Weight: 277.23
MOL File: 122-14-5.mol

Less

Fenitrothion Property

Melting point:: 3.4°C
Boiling point:: 140-145°C (0.05 torr)
Density: 1.3227
vapor pressure: 1.5 x 10^-2 Pa (20 °C)
refractive index: nD25 1.5528
Flash point:: >100 °C
storage temp.: APPROX 4°C
solubility: Chloroform (Soluble), Methanol (Soluble)
form: Liquid
Specific Gravity: 1.328 (20℃)
color: Light yellow to yellow
Water Solubility: 0.003 g/100 mL
Merck: 13,4003
BRN: 8983553
LogP: 3.319 at 25℃
CAS DataBase Reference: 122-14-5(CAS DataBase Reference)
NIST Chemistry Reference: Fenitrothion(122-14-5)
EPA Substance Registry System: Fenitrothion (122-14-5)

Less

Safety

Hazard Codes: Xn;N,N,Xn,T,F,T+
Risk Statements: 22-50/53-23-21/22-67-65-38-11-26
Safety Statements: 2-60-61-45-36/37-62-28-16
RIDADR: 3018
WGK Germany: 3
RTECS: TG0350000
HazardClass: 6.1(b)
PackingGroup: III
HS Code: 29201900
Hazardous Substances Data: 122-14-5(Hazardous Substances Data)
Toxicity: LD50 orally in rats: 250 mg/kg (Schrader)

Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Danger

Hazard statements

H301Toxic if swalloed

H312Harmful in contact with skin

H330Fatal if inhaled

H410Very toxic to aquatic life with long lasting effects

Precautionary statements

P260Do not breathe dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P273Avoid release to the environment.

P280Wear protective gloves/protective clothing/eye protection/face protection.

Less

N-Bromosuccinimide Price

Sigma-Aldrich

Product number: 45487
Product name: Fenitrothion
Purity: PESTANAL
Packaging: 250mg
Price: $97.5
Updated: 2024/03/01

TRC

Product number: F247850
Product name: Fenitrothion
Packaging: 10g
Price: $945
Updated: 2021/12/16

American Custom Chemicals Corporation

Product number: PST0000163
Product name: FENITROTHION
Purity: 95.00%
Packaging: 10G
Price: $2055.9
Updated: 2021/12/16

ChemScene

Product number: CS-0013949
Product name: Fenitrothion
Purity: ≥97.0%
Packaging: 100mg
Price: $70
Updated: 2021/12/16

ChemScene

Product number: CS-0013949
Product name: Fenitrothion
Purity: ≥97.0%
Packaging: 250mg
Price: $100
Updated: 2021/12/16

Less

Fenitrothion Chemical Properties,Usage,Production

Description

Fenitrothion is a selective acaricide and contact insecticide of low ovicidal properties. It is a brown to yellow liquid with a characteristic odour. Fenitrothion belongs to the organophosphate family of insecticides. It acts by inhibiting cholinesterase, thus it is an effective pesticide against a wide range of pests such as chewing, penetrating, and sucking insect pests. These pests include locusts, coffee leaf miners, wheat bugs, rice stem borers, grain weevils, and grain beetles on orchard fruits, cereals, cotton, forests, and vegetables. Fenitrothion is also an effective household insecticide as well as vector control agent for malaria.

History

Both Bayer Leverkusen and Sumitomo Chemical Company introduced Fenitrothion in 1959. Fenitrothion has minimal toxicity as compared to parathion, albeit with a range of insecticidal activity that is very similar. Fenitrothion is marketed in emulsifiable concentrate, dust, fogging concentrate, flowable, wettable powder formulations, and oil-based liquid spray.

Toxicity Effects

Acute Toxicity
Fenitrothion has acute toxicity to mammals, which is normally considered to be low. However, tests done on rats with doses considerably higher than those of applied for parathion reveal typical symptoms of acute poisoning. It also reduced the energy of birds in acute doses. Acute toxicity reported for a human female was a TDIo of 800 mg/kg.
Chronic Toxicity
In humans, chronic symptoms include fatigue, general malaise, headache, anorexia, and loss of memory, thirst, cramps, loss of weight, tremors, and muscular weakness. Half of the fenitrothion minimally effective dose changed the thyroid structure of a freshwater murrel.

Description

Fenitrothion is a volatile brownish-yellow oil.Molecular weight=277.25; Boiling point=(decomposes)at 140C; Freezing/Melting point=0.28C; Vapor pressure=5.3 3 10 2=mbar at 20C; Flash point=157C. HazardIdentification (based on NFPA-704 M Rating System):Health 3, Flammability 1, Reactivity 0. Insoluble in water.

Chemical Properties

Clear Yellow Oil

Chemical Properties

Pure fenitrothion is a yellowish brown liquid with an unpleasant odor. It is insoluble in water, but readily soluble in common organic solvents, such as acetone, alcohol, benzene, chlorinated hydrocarbons, dichloromethane, 2-propanol, toluene, in ethers, methanol, and xylene. It decomposes explosively. Fenitrothion is a contact insecticide and a selective acaricide of low ovicidal properties. Fenitrothion is effective against a wide range of pests, namely, penetrating, chewing, and sucking insect pests (coffee leaf-miners, locusts, rice stem borers, wheat bugs, fl our beetles, grain beetles, grain weevils) on cereals, cotton, orchard fruits, rice, vegetables, and forests. It may also be used as a fl y, mosquito, and cockroach residual contact spray for farms and public health programs. Fenitrothion is also effective against household insects and all nuisance insects. WHO confi rmed its effectiveness as a vector control agent for malaria. It is extensively used in other countries, including Japan, where parathion has been banned. Occupational workers are exposed to fenitrothion during mixing, loading/transportation, and fi eld applications.

Chemical Properties

Fenitrothion is a volatile brownish-yellow oil.

Uses

Insecticide.

Uses

Fenitrothion is used to control sucking, chewing and boring insects in cereals, soft fruit, tropical fruit, vines, sugar cane, vegetables, turf and forestry. It is also used as a public health insecticide for the control of flies, cockroaches and mosquitoes. Other uses are for the control of stored product pests and locusts.

Definition

ChEBI: An organic thiophosphate that is O,O-dimethyl O-phenyl phosphorothioate substituted by a methyl group at position 3 and a nitro group at position 4.

General Description

Brownish-yellow oil. Used as a selective acaricide and a contact and stomach insecticide against chewing and sucking insects on rice, orchard fruits, vegetables, cereals, cotton and forest. Also used against flies, mosquitoes, and cockroaches.

Reactivity Profile

Organophosphates, such as Fenitrothion, are susceptible to formation of highly toxic and flammable phosphine gas in the presence of strong reducing agents such as hydrides. Partial oxidation by oxidizing agents may result in the release of toxic phosphorus oxides.

Hazard

Cholinesterase inhibitor, use may be restricted.

Health Hazard

Fenitrothion is toxic to animals and humans. After prolonged periods of exposures to high concentrations of fenitrothion, occupational workers show poisoning. The symptoms include, but are not limited to, general malaise, fatigue, headache, loss of memory and ability to concentrate, anorexia, nausea, thirst, loss of weight, cramps, muscular weakness, and tremors, and at suffi ciently high dosage produce typical cholinergic poisoning. The formulation product, sumithion 50EC, causes delayed neurotoxicity in adult rats, as well as humans.

Health Hazard

Fenitrothion is an organophosphate insecticide. It is a highly toxic cholinesterase inhibitor, that acts on the nervous system. Does not cause delayed neurotoxicity and contact produces little irritation.

Fire Hazard

When heated to decomposition, Fenitrothion emits very toxic fumes of oxides of nitrogen, phosphorus and sulfur. Decomposition at 212-284F produces a mixture of organophosphorus polymers. Unstable in alkaline media. Stable for 2 years if stored at 68-77F. Do not store above 104F.

Flammability and Explosibility

Not classified

Agricultural Uses

Insecticide, Acaracide: Not approved for use in EU countries. Registered for use in the U.S. This is a selective acaricide and a contact and stomach insecticide. Fenitrothion is a contact insecticide and selective acaricide of low ovicidal properties. It is considered an acetylcholinesterase inhibitor. Fenitrothion is effective against a wide range of pests, i.e. penetrating, chewing and sucking insect pests (coffee leafminers, locusts, rice stem borers, wheat bugs, flour beetles, grain beetles, grain weevils) on cereals, cotton, orchard fruits, rice, vegetables, and forests. It may also be used as a fly, mosquito, and cockroach residual contact spray for farms and public health programs. Fenitrothion is also effective against household insects and all of the nuisance insects listed by the World Health Organization. Its effectiveness as a vector control agent for malaria is confirmed by the World Health Organization. Fenitrothion is non-systemic, and non-persistent. Fenitrothion was introduced in 1959 by both Sumitomo Chemical Company and Bayer Leverkusen and later by American Cyanamid Company. Fenitrothion is far less toxic than parathion with a range of insecticidal activity that is very similar and is similar enough in structure to be produced in the same factories. The difference in precursor chemicals might make it somewhat more expensive, but it is heavily used in other countries, including Japan, where parathion has been banned. Fenitrothion comes in dust, emulsifiable concentrate, flowable, fogging concentrate, granules, ULV, oil-based liquid spray, and wettable powder formultaions. It is compatible with other neutral insecticides.

Trade name

ACCOTHION®; ACEOTHION®; AGRIA 1050®; AGRIYA 1050®; AGROTHION®; AMERICAN CYANAMID CL-47,300®; ARBOGAL®; BAY 41831®; BAYER 41831®; BAYER S 5660®; CEKUTROTHION®; CL 47300®; CP47114®; CYFEN®; CYTEL®; CYTEN®; DICATHION®; DICOFEN®; DYBAR®; EI 47300®; FALITHION®; FENITEX®; FENITOX®; FENSTAN®; FOLETHION®; FOLITHION®; H-35-F 87 (BVM)®; 8057HC®; KALEIT®; KEEN SUPERKILL ANT AND ROACH EXTERMINATOR®; KILLGERM TETRACIDE INSECTICIDAL SPRAY®; KOTION®; MEP (PESTICIDE)®; METATHION®; METATHIONE®; METATION®; MICROMITE®; MONSANTO CP 47114®; NITROPHOS®; NOVATHION®; NUVAND®; NUVANOL®; OLEOSUMIFENE®; OMS 43®; OVADOFOS®; PENNWALT C-4852; PESTROY®; S 112A®; S 5660®; SMT®; SUMITHION®[C]; TURBAIR GRAIN STORAGE INSECTICIDE®; VERTHION®

Safety Profile

Poison by ingestion, inhalation, intravenous, and intraperitoneal routes. Moderately toxic by skin contact, intratracheal, and subcutaneous routes. Human systemic effects: coma, diarrhea, dyspnea, gastrointestinal changes, hypermodtty, nausea or vomiting, respiratory depression. Mutation data reported. When heated to decomposition it emits very toxic fumes of NOx, POx, and sox

Potential Exposure

A potential danger to those involved in the manufacture, formulation, and application of this insecticide. It is a selective acaricide; and a contact and stomach insecticide. Used to control chewing and sucking insects on rice, orchard fruit; vegetables, cereals, cotton, and in forests. Also protects against flies, mosquitoes, and cockroaches

First aid

If this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts theskin, remove contaminated clothing and wash immediatelywith soap and water. Speed in removing material from skinis of extreme importance. Shampoo hair promptly if contaminated. Seek medical attention immediately. If this chemical has been inhaled, remove from exposure, beginrescue breathing (using universal precautions, includingresuscitation mask) if breathing has stopped and CPR ifheart action has stopped. Transfer promptly to a medicalfacility. When this chemical has been swallowed, get medical attention. Give large quantities of water and inducevomiting. Do not make an unconscious person vomit.Effects may be delayed. Keep victim under medicalobservation.

Metabolic pathway

Fenitrothion is a non-systemic insecticide, the biotransformations and environmental fate of which have been intensively studied and reviewed. Metabolism has been studied in mammals (including humans), birds, fish, crustacea, molluscs, insects, algae, plants and soil. The major routes of biotransformation involve desulfuration to the oxon analogue (fenitrooxon) and hydrolysis to give dimethyl phosphate, O,O-dimethyl phosphorothioate and 3-methyl-4-nitrophenol. Demethylation to give desmethylfenitrothion and its decomposition products, reduction of the nitro group and oxidation of the ring methyl group also occur. Demethylation via glutathione-S-methyl transferases in the liver is a particularly important mechanism in mammals. Reduction of the nitro group to an amino group is important in anaerobic soils and ruminants but this has also been shown to occur in rats, rabbits and humans where it is presumably carried out by bacteria in the gut. Oxidation of the 3-methyl group to hydroxymethyl and carboxylate has been shown to be a degradative route in birds. The major routes of phase II metabolism involve conjugation of 3-methyl-4-nitrophenol to the glucoside in plants and insects, to the sulfate ester in birds and the sulfate ester and glucuronide in mammals.

Metabolism

The main biotransformation routes involve oxidative desulfuration to the oxon and dearylation to give dimethyl hydrogen phosphate, O,O-dimethyl hydrogen phosphorothioate and 3-methyl-4-nitrophenol. Demethylation dependent on glutathion-S-alkyl transferase is particularly important in mammals.Oxidation of the 3-methyl group to hydroxymethyl and then carboxyl group is also a degradative route. Reduction of the nitro group to an amino group occurs in anaerobic soils and ruminants. The DT₅₀ in soils under upland and submerged conditions were 12–28 and 4–20 d, respectively.

storage

Color Code—Blue: Health Hazard/Poison: Store ina secure poison location. Prior to working with this chemicalyou should be trained on its proper handling and storage.Prior to working with this chemical you should be trained onits proper handling and storage. Store in tightly closed containers in a cool, well-ventilated area away from oxidizers.Where possible, automatically pump liquid from drums orother storage containers to process containers.

Shipping

UN3017 Organophosphorus pesticides, liquid, toxic, flammable, flash point not ,23C, Hazard class: 6.1; Labels: 6.1-Poisonous materials, 3-Flammable liquid. UN2810 Toxic liquids, organic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required

Toxicity evaluation

The acute oral LD₅₀ values in mammals range from 330 mg/kg in rats to 1850 mg/kg in the guineapig. Inhalation LC50 (4 h) for rats is >1.2 mg/L air. NOEL (2 y) for rats and mice is 10 mg/kg diet (0.5 mg/kg/d). ADI is 5 μg/kg b.w.

Degradation

Fenitrothion is relatively stable to hydrolysis under normal conditions (PM). Mikami et al. (1985) reported the hydrolysis of fenitrothion between pH 5 and 10. Below pH 7 hydrolysis occurred by a pH-independent mechanism and above pH 9 by a base-catalysed process. At intermediate pH values both mechanisms were operative. The major mechanism below pH 8 was demethylation to give desmethylfenitrothion and above pH 9, cleavage of the P-O-aryl bond gave 3-methyl-4-nitrophenol.

Incompatibilities

Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases,strong acids, oxoacids, epoxides. Strong oxidizers may cause release of toxic phosphorus oxides. Organophosphates, in the presence of strong reducing agents such as hydrides, may form highly toxic and flammable phosphine gas. Keep away from alkaline materials

Waste Disposal

Incineration (for large amounts); alkaline hydrolysis and landfill (for small amounts). In accordance with 40CFR165, follow recommendations for the disposal of pesticides and pesticide containers. Must be disposed properly by following package label directions or by contacting your local or federal environmental control agency, or by contacting your regional EPA office.

Fenitrothion Preparation Products And Raw materials

Raw materials

Petroleum crude oil 3-Methyl-4-nitrophenol O-methyl dichlorothiophosphate THIOPHOSPHORYL CHLORIDE Dimethyl sulfide Copper(I) chloride Hydrochloric acid Nitric acid m-Cresol Methanol Sodium nitrate

Preparation Products

Fenthion Malathion+Fenitrothion,E.C. CYANOPHOS Chlorpyrifos-methyl

Less

Fenitrothion Suppliers

Canada 2 China 194 France 2 Germany 3 India 3 Japan 6 Norway 1 Switzerland 1 United Kingdom 5 United States 22 Global 239

Shandong Debek Bioengineering Co. LTD

Tel: 13854830608; 13854830608
Email: 13854830608@163.com
Country: China
ProdList: 1462
Advantage: 58

J & K SCIENTIFIC LTD.

Tel: 010-82848833 400-666-7788
Fax: 86-10-82849933
Email: jkinfo@jkchemical.com
Country: China
ProdList: 96815
Advantage: 76

TAIYUAN RHF CO.,LTD.

Tel: +86 351 7031519
Fax: +86 351 7031519
Email: sales@RHFChem.com
Country: China
ProdList: 2338
Advantage: 56

Capot Chemical Co., Ltd

Tel: +86 (0) 571 85 58 67 18
Fax: 0086-571-85864795
Email: sales@capotchem.com
Country: China
ProdList: 18207
Advantage: 66

Wuhan Wei Shunda Technology Development Co., Ltd.

Tel: 86-027-88774375
Fax: 86-027-88416321
Email: mwmwhot@163.com
Country: China
ProdList: 233
Advantage: 65

Chemsky（shanghai）International Co.,Ltd.

Tel: 021-50135380
Email: shchemsky@sina.com
Country: China
ProdList: 32321
Advantage: 50

Syntechem Co.,Ltd

Tel
Fax: E-Mail Inquiry
Email: info@syntechem.com
Country: China
ProdList: 12984
Advantage: 57

Sichuan Kulinan Technology Co., Ltd

Tel: 400-1166-196 18981987031
Fax: 028-84555506 800101999
Email: cdhxsj@163.com
Country: China
ProdList: 11707
Advantage: 57

9ding chemical ( Shanghai) Limited

Tel: 4009209199
Fax: 86-021-52271987
Email: sales@9dingchem.com
Country: China
ProdList: 22514
Advantage: 55

Shanghai Aladdin Bio-Chem Technology Co.,LTD

Tel: 400-400-6206333 18521732826
Fax: 021-50323701
Email: market@aladdin-e.com
Country: China
ProdList: 25003
Advantage: 65

Nanjing Sunlida Biological Technology Co., Ltd.

Tel: 025-57798810
Fax: 025-57019371
Email: sales@sunlidabio.com
Country: China
ProdList: 3239
Advantage: 55

TargetMol Chemicals Inc.

Tel: 021-021-33632979 15002134094
Fax: 021-33632979
Email: marketing@targetmol.com
Country: China
ProdList: 7783
Advantage: 58

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: 4511
Advantage: 55

Codow Chemical Co.,Ltd.

Tel: 18620099427 18620099427
Fax: +86-20-62619665
Email: amy@howeipharm.com
Country: China
ProdList: 1751
Advantage: 55

Chemwill Asia Co.,Ltd.

Tel: 86-21-51086038
Fax: 86-21-51861608
Email: sales@chemwill.com
Country: China
ProdList: 1974
Advantage: 58

Shanghai Xilong Biochemical Technology Co., Ltd.

Tel: 021-52907766-8042
Fax: 021-52906523
Country: China
ProdList: 9941
Advantage: 58

Grader reagent

Tel: 18221735425
Email: sales@xinpingchem.com
Country: China
ProdList: 9942
Advantage: 58

Beijing Jin Ming Biotechnology Co., Ltd.

Tel: 010-60605840 18892239720
Fax: 010-60605840
Email: psaitong@jm-bio.com
Country: China
ProdList: 12306
Advantage: 58

Guangzhou Kafen Biotech Co.,Ltd

Tel: 18029243487 2355327168
Fax: 020-31121510
Email: gy@yccreate.com
Country: China
ProdList: 4749
Advantage: 55

Wuhai Shuou Technology Co., Ltd.

Tel: 17792809151
Fax: 18872220797
Email: 2355916837@ycphar.com
Country: China
ProdList: 6133
Advantage: 55

Taian Jiaye Biotechnology Co.Ltd

Tel: 13127280945
Email: 285424065@qq.com
Country: China
ProdList: 9976
Advantage: 55

Shanghai Orgchem Co.,Ltd.

Tel: +86-21-5877 1921
Fax: +86-21-5877 1925
Email: info@chemofchina.com
Country: China
ProdList: 9653
Advantage: 55

Shandong Ono Chemical Co., Ltd.

Tel: 0539-6362799 20）
Fax: 0539-6362799（To 20）
Country: China
ProdList: 9998
Advantage: 58

9ding chemical ( Shanghai) Limited

Tel: 021-021-52271985 17721149837
Fax: +86 (21) 52271987
Email: sales@9dingchem.com
Country: China
ProdList: 19800
Advantage: 60

Shanghai BaiShun Biological Technology Co., Ltd

Tel: 021-37581181
Fax: 021-57456066
Email: sales@chem-mall.com
Country: China
ProdList: 10330
Advantage: 58

Shenzhen Regent Biochemical Technology Co., Ltd.

Tel: 0755-0755-85201366 18938635012
Fax: 0755-85201366
Email: sales@regentsciences.com
Country: China
ProdList: 9355
Advantage: 58

Capot Chemical Co.,Ltd.

Tel: +86-（0）57185586718 +86-13336195806
Fax: +86-571-85864795
Email: sales@capot.com
Country: China
ProdList: 29791
Advantage: 60

Shanghai Jizhi Biochemical Technology Co. Ltd.

Tel: 4009004166/18616739031 18616739031
Email: 3007523370@qq.com
Country: China
ProdList: 52693
Advantage: 58

Beijing altar ink quality inspection technology co., LTD

Tel: 010-52889049
Email: 2250970673@qq.com
Country: CHINA
ProdList: 1132
Advantage: 58

Shanghai Hongye Biotechnology Co. Ltd

Tel: 400-9205774
Email: sales@glpbio.cn
Country: China
ProdList: 6777
Advantage: 58

Shenzhen Polymeri Biochemical Technology Co., Ltd.

Tel: +86-400-002-6226 +86-13028896684;
Email: sales@rrkchem.com
Country: China
ProdList: 57412
Advantage: 58

Hefei TNJ Chemical Industry Co.,Ltd.

Tel: +86-0551-65418671 +8618949823763
Fax: 0551-65418697
Email: sales@tnjchem.com
Country: China
ProdList: 34553
Advantage: 58

AFINE CHEMICALS LIMITED

Tel: +86-0571-85134551
Fax: 008657185134895
Email: sales@afinechem.com
Country: China
ProdList: 15352
Advantage: 58

Hubei Jusheng Technology Co.,Ltd.

Tel: 18871490254
Fax: 027-59599243
Email: linda@hubeijusheng.com
Country: CHINA
ProdList: 28172
Advantage: 58

Xibao Biotechnology (Shanghai) Co., Ltd.

Tel: 13761246140
Email: 58642714@qq.com
Country: China
ProdList: 415
Advantage: 58

Hubei xin bonus chemical co. LTD

Tel: 86-13657291602
Fax: 027-59338440
Email: linda@hubeijusheng.com
Country: CHINA
ProdList: 22963
Advantage: 58

Shandong chuangyingchemical Co., Ltd.

Tel: 18853181302
Email: sale@chuangyingchem.com
Country: CHINA
ProdList: 5906
Advantage: 58

Wuhan xinyangruihe Chemical Technology Co., Ltd.

Tel: 153-07155313 15307155313
Fax: QQ：2274366233
Email: 2274366233@qq.com
Country: China
ProdList: 4997
Advantage: 58

Chongqing Chemdad Co., Ltd

Tel: +86-023-6139-8061 +86-86-13650506873
Email: sales@chemdad.com
Country: China
ProdList: 39894
Advantage: 58

Nanjing Bermuda Biotechnology Co., Ltd.

Tel: 027-1734052141618086404407 17340521416
Fax: 17340521416
Email: 1757224788@qq.com
Country: China
ProdList: 2003
Advantage: 58

Wuhan Rongcan Biotechnology Co., Ltd

Tel: 18327024450
Fax: 183-27024450
Email: 2130026275@qq.com
Country: China
ProdList: 4570
Advantage: 58

CONIER CHEM AND PHARMA LIMITED

Tel: +8618523575427
Email: sales@conier.com
Country: China
ProdList: 49374
Advantage: 58

ShangHai Anpel Co, Ltd.

Tel: 18501792038; 18501792038
Email: shanpel@anpel.com.cn
Country: China
ProdList: 9611
Advantage: 58

Wuhan kemike Biomedical Technology Co., Ltd

Tel: 13163388153 13163388153
Email: yeqiu416@163.com
Country: China
ProdList: 9898
Advantage: 58

Shanghai Sig Biotechnology Co., LTD

Tel: 021-57810052 18930344717
Fax: 021-57810052
Email: 2089316240@qq.com
Country: China
ProdList: 9395
Advantage: 58

Wuhan plov Biotechnology Co., Ltd

Tel: 17612776928
Fax: 17612776928
Email: 17612776928@qq.com
Country: China
ProdList: 4971
Advantage: 58

Hubei MAX Fine Chemical Technology Co., Ltd.

Tel: 13026126800 13027176014
Fax: QQ1652805836
Email: hbmaxkj@163.com
Country: China
ProdList: 4728
Advantage: 58

Energy Chemical

Tel: 021-58432009 400-005-6266
Fax: 021-58436166
Email: marketing1@energy-chemical.com
Country: China
ProdList: 44808
Advantage: 58

Shandong Suihua Biotechnology Co. Ltd

Tel: 15689727968
Email: freesky2121@163.com
Country: China
ProdList: 961
Advantage: 58

Less

View Lastest Price from Fenitrothion manufacturers

Hebei Zhuanglai Chemical Trading Co.,Ltd

Product: Fenitrothion 122-14-5
Price: US $60.00/kg
Min. Order: 1kg
Purity: 99%
Supply Ability: 5000kg/week
Release date: 2024-05-23

qingdao trust agri chemical co.,ltd

Product: fenitrothion 122-14-5
Price: US $0.00/kg
Min. Order: 1kg
Purity: 99
Supply Ability: 20tons
Release date: 2024-07-24

Shaanxi Dideu Medichem Co. Ltd

Product: Fenitrothion 122-14-5
Price: US $0.00-0.00/KG
Min. Order: 1KG
Purity: 99.0%
Supply Ability: 500 tons
Release date: 2020-04-27

122-14-5, FenitrothionRelated Search:

Dimethyl sulfate Methyl acrylate Dimethyl carbonate Clindamycin phosphate Diphenylthiocarbazide Dimethyl fumarate Azamethiphos Dimethyl disulfide Dimethyl sulfoxide 1-Phenyl-2-nitropropene Dacthal ETHANE Dimethyl ether Acetylsalicylic acid N,N-Dimethylformamide Chlorodimethylphenylsilane Parathion-methyl FENITROTHION (O,O-DIMETHYL-D6),(O,O-DIMETHYL D6) FENITROTHION D6,FENITROTHION D6,FENITROTHION-D6 (O,O-DIMETHYL-D6)

SUMITHION

SUMITHION(R)

Phosphorothioic acid O,O-dimethyl O-(3-methyl-4-nitrophenyl) ester

O,O-DIMETHYL O-(3-METHYL-4-NITROPHENYL) PHOSPHOROTHIOATE

O,O-DIMETHYL-O-(4-NITRO-M-TOLYL)-PHOSPHOROTHIOATE

Nitrophos

Nuvanol

nuvanol/n-20

3-methyl-4-nitrophenyldimethylphosphorothioate

8057hc

AC-47300

Accothion

Aceothion

Agria 1050

agria1050

Agriya 1050

agriya1050

Akotion

dimethyl4-nitro-m-tolylphosphorothionate

EI 47300

ei47300

ENT 25,715

ent25,715

Falithion

Fenitex

fenition

Fenitrothion EC

Fenitrotion

fenitrotion(hungarian)

fentrothione

Folithion ec 50

folithionec50

FENITROTHIO

novathion

fenitrothion (bsi,iso,esa,ban)

fenitrothion solution

mep (jmaf)

FENTROTHION

O,O-DIMETHYLO-(4-NITRO-META-TOLYL)-PHOSPHOROTHIOATE

SUMITHION50EC

DIMETHYL4-NITRO-META-TOLYLPHOSPHOROTHIONATE

FENITROTHION, 250MG, NEAT

FENITROTHION PESTANAL (O,O-DIMETHYL O-4-

FENITROTHION, 500MG, NEAT

fenitrothion (ISO) O,O-dimethyl O-4-nitro-m-tolyl phosphorothioate

EphB6/Fc Chimera from mouse

dimethoxy-(3-methyl-4-nitro-phenoxy)-sulfanylidene-$l^{5}-phosphane

dimethoxy-(3-methyl-4-nitrophenoxy)-sulfanylidene-$l^{5}-phosphane

dimethoxy-(3-methyl-4-nitro-phenoxy)-thioxo-phosphorane

Fenstan

American cyanamid cl-47,300

americancyanamidcl-47,300

BAY S 5660

Bayer S 5660

bayers5660

Cekutrothion

CL 47300

cl47300