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Allethrin

Allethrin Structure
CAS No.
584-79-2
Chemical Name:
Allethrin
Synonyms
Esbioi;fmc249;nia249;oms468;D-TRANS;exthrin;fda1446;FMC 249;NIA 249;OMS 468
CBNumber:
CB6681269
Molecular Formula:
C19H26O3
Molecular Weight:
302.41
MOL File:
584-79-2.mol
MSDS File:
SDS
Modify Date:
2023/9/26 17:18:59

Allethrin Properties

Melting point approximate 4℃
Boiling point 160°C
Density 1.01
vapor pressure 1.6×10-4 Pa (21 °C)
refractive index nD20 1.5040; nD30 1.5023
Flash point 66 °C
storage temp. 2-8°C
solubility Chloroform: Slightly Soluble
form Viscous Liquid
Water Solubility 2 mg l-1
color Clear amber
BRN 2294836
LogP 4.780
CAS DataBase Reference 584-79-2(CAS DataBase Reference)
NIST Chemistry Reference Bioallethrin(584-79-2)
EPA Substance Registry System Allethrin (584-79-2)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07,GHS09
Signal word  Warning
Hazard statements  H302+H332-H410
Precautionary statements  P273-P301+P312+P330-P304+P340+P312
Hazard Codes  Xn;N,N,Xn
Risk Statements  20/22-50/53-40
Safety Statements  36-60-61-36/37-24/25-23
RIDADR  UN 3082
WGK Germany  3
RTECS  GZ1925000
HazardClass  6.1(b)
PackingGroup  III
HS Code  29183000
Toxicity LD50 oral in rabbit: 4290mg/kg
NFPA 704
1
1 0

Allethrin price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 33396 Allethrin PESTANAL?, analytical standard 584-79-2 100MG ₹5964.58 2022-06-14 Buy
Sigma-Aldrich(India) 33309 Esbiothrin PESTANAL?, analytical standard 584-79-2 100MG ₹5228.48 2022-06-14 Buy
Sigma-Aldrich(India) 31489 Bioallethrin PESTANAL?, analytical standard 584-79-2 250MG ₹4481.55 2022-06-14 Buy
Product number Packaging Price Buy
33396 100MG ₹5964.58 Buy
33309 100MG ₹5228.48 Buy
31489 250MG ₹4481.55 Buy

Allethrin Chemical Properties,Uses,Production

Chemical Properties

Yellow Oil

Uses

Allethrin is a synthetic pyrethroid derivative used as an insecticide. Allethrin is commonly used in many household insecticide products due to its low toxicity towards humans.

Definition

Generic name for 2-allyl4-hydroxtcyclopenten-1-one ester of chrysanthemummonocarboxylic acid. A synthetic insecticide structurally similar to pyrethrin and used in the same manner. For other synthetic analogs, see barthrin, cyclethrin, ethythrin, furethrin. Pyrethrin I differs in having a 2,4-pentadienyl group in place of the allyl of allethrin.

General Description

A clear amber-colored viscous liquid. Insoluble and denser than water. Toxic by ingestion, inhalation, and skin absorption. A synthetic household insecticide that kills flies, mosquitoes, garden insects, etc.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

Allethrin is an ester and ketone. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides. Ketones are reactive with many acids and bases liberating heat and flammable gases (e.g., H2). The amount of heat may be sufficient to start a fire in the unreacted portion of the ketone. Ketones react with reducing agents such as hydrides, alkali metals, and nitrides to produce flammable gas (H2) and heat. Ketones are incompatible with isocyanates, aldehydes, cyanides, peroxides, and anhydrides. They react violently with aldehydes, HNO3, HNO3 + H2O2, and HClO4.

Health Hazard

Highly toxic, may be fatal if inhaled, swallowed or absorbed through skin. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.

Fire Hazard

Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Containers may explode when heated. Runoff may pollute waterways.

Agricultural Uses

Insecticide: Allethrin is used almost exclusively to control flying and crawling insects in homes and industrial locations. Used extensively in pet animal shampoos, to treat lice in humans and in home and industrial sprays for flying insects, mosquitos, etc. It is available as mosquito coils, mats, oil formulations and as an aerosol spray. It may be hazardous to the environment; special attention should be given to fish and honey bees. Not currently registered in the U.S. Not approved for use in EU countries. Depending on CAS registry number there are probably >100 global suppliers.

Trade name

BIOALLETHRIN®; BIOALLETHRIN TECHNICAL®; d-CISALLETHRIN®; ESBIOTHRIN®; EXTHRIN® FMC 249®; NIA 249®; OMS 468®; PYNAMIN®; PYNAMIN-FORTE®; PYRESIN®; PYRESYN®; PYREXCEL®; PYROCIDE®; SBP 1382/ BIOALLETHRIN CONCENTRATE®

Contact allergens

Pyrethroids, also called pyrethrinoids, are neurotoxic synthetic compounds used as insecticides, with irritant properties. Cypermethrin and fenvalerate have been reported as causing positive allergic patch tests, but only fenvalerate was relevant in an agricultural worker.

Safety Profile

Poison by intravenous, intracerebral, and intraperitoneal routes. Moderately toxic by ingestion and skin contact. An allergen. An insecticide. It can cause liver and kidney damage by all routes of entry into the body. Lung congestion may occur due to exposure. Local contact may cause contact dermatitis. Inhalation may cause asthma, coughing, wheezing, running nose and eyes. Mutation data reported. See also ALLYL COMPOUNDS and ESTERS. Slight fire hazard. When heated to decomposition it emits acrid fumes.

Metabolic pathway

Allethrin was the first synthetic pyrethroid. Its stereochemistry is RS(cyclopentenyl)lRcis-trans. It was further developed as bioallethrin (RSlRtvuns) and then as S-bioallethrin (SlRtvuns), the most potent of the three. All are very sensitive to light and are used almost entirely indoors. Thus, there is only a limited amount of information on their environmental fate published in the literature. Information on photodegradation and on metabolism in insects and rodents has been reported.

Global( 206)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
Shogun Organics Ltd +91-2266776846 +91-2266776845 Maharashtra, India 8 58 Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
A.J Chemicals 91-9810153283 New Delhi, India 6124 58 Inquiry
Pharmaffiliates Analytics and Synthetics P. Ltd +91-172-5066494 Haryana, India 6773 58 Inquiry
Vallabh Pesticides Limited 08048372724Ext 120 Gujarat, India 5 58 Inquiry
M/S Ahmad Beez Store 08048250244Ext 776 Uttar Pradesh, India 1 58 Inquiry
Solex Chemicals Private Limited 08068979890Ext 189 Kolkata, India 1 58 Inquiry
Pharma Affiliates 172-5066494 Haryana, India 6761 58 Inquiry
Henan Tianfu Chemical Co.,Ltd. +86-0371-55170693 +86-19937530512 China 21675 55 Inquiry
Hefei TNJ Chemical Industry Co.,Ltd. +86-0551-65418679 +86-18949832763 China 2989 55 Inquiry
(.+/-.)-3-Allyl-2-methyl-4-oxocyclopent-2-enyl 2,2-dimethyl-3-(2-methylprop-1-enyl) cyclopropylcarboxylate 2,2-dimethyl-3-(2-methylpropenyl)-cyclopropanecarboxylicaciesterwith2-a BIOALLETHRINE BIOALLETHRIN D-TRANS (+-)-3-allyl-2-methyl-4-oxocyclopent-2-enyl 2,2-dimethyl-3-(2-methylpropen-1-yl)cyclopropanecarboxylate (R,S)-3-ally-2-methyl-4-oxo-cyclopent-2-enyl-(1R)-chrysanthemate ALLETHRIN MIXTURE OF STEREO ISOMERS, PES ALLETHRIN MIXTURE OF STEREO ISOMERS,PEST ALLETHRIN, 1X5ML, 0.1MG/ML IN METHYLENE CHLORIDE Allethrin(0.1mg/mlinMethylenechloride) allethrin (bsi,e-iso,esa,jmaf) allethrin solution allethrine (f-iso) allylcinerine bioallethrin (bsi) d-allethrin (bsi,e-iso,esa,jmaf) depalléthrin (f) ES-ALLETHRIN 2-Allyl-3-methyl-1-oxocyclopenten-2-yl-4-obic ester syc, trans-xrizantemobic acid D-TRANS ALLETHRI BIO(D-TRANS)ALLETHRIN Pynamine Rous-sel-Uclaf (RS)-3-Allyl-2-methyl-4-oxocyclopent-2-enyl (1R)-cis-trans-chrysanthemate 2,2-Dimethyl-3-(2-methyl-1-propenyl)cyclopropane-1-carboxylic acid 2-methyl-4-oxo-3-(2-propenyl)-2-cyclopentenyl ester 2,2-Dimethyl-3-(2-methyl-1-propenyl)cyclopropane-1-carboxylic acid 3-allyl-2-methyl-4-oxo-2-cyclopenten-1-yl ester 2,2-Dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylic acid 2-methyl-4-oxo-3-(2-propenyl)-2-cyclopenten-1-yl 2,2-Dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylic acid 2-methyl-4-oxo-3-(2-propenyl)-2-cyclopenten-1-yl ester (RS)-3-allyl-2-methyl-4-oxocyclopent-2-enyl (1RS,3RS:1RS,3SR)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate,(RS)-3-allyl-2-methyl-4-oxocyclopent-2-enyl (1R,3R)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate,allethrin,bioallethr (+/-)-2,2-Dimethyl-3-(2-methylpropenyl)cyclopropanecarboxylic Acid Ester with 2-allyl-4-hydroxy-3-methyl-2-cyclopenten-1-one 2-Methyl-4-oxo-3-(2-propenyl)-2-cyclopenten-1-yl 2,2-dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarborylate Bioallathrin 2,2-dimethyl-3-(2-methyl-1-propenyl)-,2-methyl-4-oxo-3-(2-propenyl)-2-cyclopenten-1-yl ester Allethrin Solution 0.1mg/ml in Methylene chloride 5ml [584-79-2] 2-Methyl-4-oxo-3-(prop-2-en-1-yl)cyclopent-2-en-1-yl 2,2-diMethyl-3-(2-Methylprop-1-en-1-yl)cyclopropane-1-carboxylate 2,2-diMethyl-3-(2-Methyl-1-propen-1-yl)-cyclopropanecarboxylic Acid 2-Methyl-4-oxo-3-(2-propen-1-yl)-2-cyclopenten-1-yl Ester Esbiothrine NSC 11782 2-methyl-4-oxo-3-(2-propenyl)-2-cyclopenten-1-yl-2',2'-dimethyl-3'-(2-methyl-1-peopenyl)cyclopropanecarboxylate Esbioi D-Allethrin 0 ethyl-3-(2-methylpropenyl)-cyclopropanecarboxylicacid exthrin FDA 1446 fda1446 FMC 249 fmc249 llyl-4-hydroxy-3-methyl-2-cyclopenten-1-one Necarboxylic acid necarboxylicacid NIA 249 nia249 nocarboxylate OMS 468 oms468 -oxo-3-(2-propenyl)-2-cyclopenten-1-ylester oxo-3-(2-propenyl)-2-cyclopenten-1-ylester