S-BIOALLETHRIN（CAS 22431-63-6）：分子式 C19H26O3、分子量 302.4；类别 有机化学品。
| CAS号 | 22431-63-6 |
|---|---|
| 分子式 | C19H26O3 |
| 分子量 | 302.4 |
| 熔点 | ~4 °C |
| 沸点 | at 0.013kPa: 140 °C |
| LogP | 4.78 |
| 应用领域 | Uses: Used in homes and gardens to kill flies and mosquitoes、The d-trans isomer is a more potent insecticide used to control animal parasites. Sold as mosquito coils、mats、oil formulations、and sprays、[EXTOXNET]、Farming (Pesticides) [Category: Industry]、For Allethrin、(the product that is a mixture)、(USEPA、OPP Pesticide Code: 004001) there are 0 labels match.、SRP: Not registered for current use in the U.S.、but approved pesticide uses may change periodically and so federal、state and local authorities must be consulted for currently approved uses.、Allethrin、For bioallethrin (USEPA、OPP Pesticide Code: 004003) ACTIVE products with label matches.、SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal、Bioallethrin、For S-bioallethrin (USEPA、OPP Pesticide Code: 004004) ACTIVE products with label matches.、S-Bioallethrin、For d-trans-allethrin (USEPA、d-trans-Allethrin、For more Uses (Complete) data for ALLETHRINS (14 total)、please visit the HSDB record page.、Use (kg、approx.) in Germany (2009): >10、Consumption (g per capita、approx.) in Germany (2009): 0.000122、Calculated removal (%): 92.4、Pyrethroids are used as insecticides. (L857)、Use Classification: INSECTICIDES、INSECTICIDES、Household Products: Information on 9 consumer products that contain d-trans-Allethrin in the following categories is provided:、• Inside the Home、• Pesticides、• Pet Care、Information on 21 consumer products that contain d-trans Allethrin in the following categories is provided:、• Personal Care、Information on 5 consumer products that contain d-cis、trans-Allethrin in the following categories is provided:、Methods of Manufacturing: Allethrin is prepared by the esterification of (1RS、3RS or cis、trans)-2、2-dimethyl-3-(2、2-dimethylvinyl) cyclopropanecarboxylic acid or chrysanthemic acid with (1RS)-3- allyl-2-methyl-4-oxocyclopent-2-ene-1-ol or allethrolone ... .、2-Allyl-3-methyl-2-cyclopenten-4-ol-1-one (allethrone) and chrysanthemum monocarboxlic anhydride in dibutyl ether at 150-175 °C for 3-6 hr are reacted. Upon cooling、the solution is diluted、the chrysanthemum moncarboxlic acid byproduct is removed by saponification、the organic phase is washed with water、and the solvent evaporated.、Formulations、Preparations: USEPA、OPP Pesticide Code: 004001、Trade Names: ENT 16275、ENT 17510、FDA 1446、FMC 249、NIA 249、Pyresin、Pynamin、Exthrin.、Aerosol dispenser、emulsifiable concentrate、dispersible powder、wettable powder、Coil、d-Allethrin is greater than、equal to 95% (1R)-isomers and greater than、equal to 75% trans isomers、Grades: 90% technical (approx 90% pure、with 10% of isomers or related cmpd)、20% technical、2.5% technical.、For more Formulations、Preparations (Complete) data for ALLETHRINS (268 total)、Consumption Patterns: Less than 30、000 lbs are marketed on average per year、Allethrins、General Manufacturing Information: Cyclopropanecarboxylic acid、2、2-dimethyl-3-(2-methyl-1-propen-1-yl)-、2-methyl-4-oxo-3-(2-propen-1-yl)-2-cyclopenten-1-yl ester: ACTIVE、The WHO Recommended Classification of Pesticides by Hazard identifies Allethrin (technical grade) as Class III: slightly hazardous、Main Use: insecticide.、The first pyrethroid pesticide、allethrin、was identified in 1949. Allethrin and other pyrethroids with a basic cyclopropane carboxylic ester structure are type I pyrethroids. ... All pyrethroids can exist as at least four stereoisomers、each with different biological activities. They are marketed as racemic mixtures or as single isomers. In commercial formulations、the activity of pyrethroids is usually enhanced by the addition of a synergist such as piperonyl butoxide、which inhibits metabolic degradation of the active ingredient.、ALLETHRIN IS ALLYL HOMOLOG OF CINERIN I、WHICH IS ONE OF THE CONSTITUENTS OF PYRETHRUM、OLDEST KNOWN INSECTICIDE.、Pyrethroids、are modern synthetic insecticides similar chemically to natural pyrethrins、but modified to increase stability in the natural environment.、For more General Manufacturing Information (Complete) data for ALLETHRINS (11 total) |
| 类别 | Organic Chemicals |
登记用途：Uses: Used in homes and gardens to kill flies and mosquitoes、The d-trans isomer is a more potent insecticide used to control animal parasites. Sold as mosquito coils、mats、oil formulations、and sprays、[EXTOXNET]、Farming (Pesticides) [Category: Industry]、For Allethrin、(the product that is a mixture)、(USEPA、OPP Pesticide Code: 004001) there are 0 labels match.、SRP: Not registered for current use in the U.S.、but approved pesticide uses may change periodically and so federal、state and local authorities must be consulted for currently approved uses.、Allethrin、For bioallethrin (USEPA、OPP Pesticide Code: 004003) ACTIVE products with label matches.、SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal、Bioallethrin、For S-bioallethrin (USEPA、OPP Pesticide Code: 004004) ACTIVE products with label matches.、S-Bioallethrin、For d-trans-allethrin (USEPA、d-trans-Allethrin、For more Uses (Complete) data for ALLETHRINS (14 total)、please visit the HSDB record page.、Use (kg、approx.) in Germany (2009): >10、Consumption (g per capita、approx.) in Germany (2009): 0.000122、Calculated removal (%): 92.4、Pyrethroids are used as insecticides. (L857)、Use Classification: INSECTICIDES、INSECTICIDES、Household Products: Information on 9 consumer products that contain d-trans-Allethrin in the following categories is provided:、• Inside the Home、• Pesticides、• Pet Care、Information on 21 consumer products that contain d-trans Allethrin in the following categories is provided:、• Personal Care、Information on 5 consumer products that contain d-cis、trans-Allethrin in the following categories is provided:、Methods of Manufacturing: Allethrin is prepared by the esterification of (1RS、3RS or cis、trans)-2、2-dimethyl-3-(2、2-dimethylvinyl) cyclopropanecarboxylic acid or chrysanthemic acid with (1RS)-3- allyl-2-methyl-4-oxocyclopent-2-ene-1-ol or allethrolone ... .、2-Allyl-3-methyl-2-cyclopenten-4-ol-1-one (allethrone) and chrysanthemum monocarboxlic anhydride in dibutyl ether at 150-175 °C for 3-6 hr are reacted. Upon cooling、the solution is diluted、the chrysanthemum moncarboxlic acid byproduct is removed by saponification、the organic phase is washed with water、and the solvent evaporated.、Formulations、Preparations: USEPA、OPP Pesticide Code: 004001、Trade Names: ENT 16275、ENT 17510、FDA 1446、FMC 249、NIA 249、Pyresin、Pynamin、Exthrin.、Aerosol dispenser、emulsifiable concentrate、dispersible powder、wettable powder、Coil、d-Allethrin is greater than、equal to 95% (1R)-isomers and greater than、equal to 75% trans isomers、Grades: 90% technical (approx 90% pure、with 10% of isomers or related cmpd)、20% technical、2.5% technical.、For more Formulations、Preparations (Complete) data for ALLETHRINS (268 total)、Consumption Patterns: Less than 30、000 lbs are marketed on average per year、Allethrins、General Manufacturing Information: Cyclopropanecarboxylic acid、2、2-dimethyl-3-(2-methyl-1-propen-1-yl)-、2-methyl-4-oxo-3-(2-propen-1-yl)-2-cyclopenten-1-yl ester: ACTIVE、The WHO Recommended Classification of Pesticides by Hazard identifies Allethrin (technical grade) as Class III: slightly hazardous、Main Use: insecticide.、The first pyrethroid pesticide、allethrin、was identified in 1949. Allethrin and other pyrethroids with a basic cyclopropane carboxylic ester structure are type I pyrethroids. ... All pyrethroids can exist as at least four stereoisomers、each with different biological activities. They are marketed as racemic mixtures or as single isomers. In commercial formulations、the activity of pyrethroids is usually enhanced by the addition of a synergist such as piperonyl butoxide、which inhibits metabolic degradation of the active ingredient.、ALLETHRIN IS ALLYL HOMOLOG OF CINERIN I、WHICH IS ONE OF THE CONSTITUENTS OF PYRETHRUM、OLDEST KNOWN INSECTICIDE.、Pyrethroids、are modern synthetic insecticides similar chemically to natural pyrethrins、but modified to increase stability in the natural environment.、For more General Manufacturing Information (Complete) data for ALLETHRINS (11 total)。
S-BIOALLETHRIN 是一种以碳骨架为基础的有机化合物，登记 CAS 号为 22431-63-6，分子式 C19H26O3（分子量 302.4），归属于有机化学品大类化工原料。
登记 CAS 号：22431-63-6
其分子式 C19H26O3 由 19 个碳、26 个氢、3 个氧 组成。
别名/同义词：S-BIOALLETHRIN · Allethrins
所属分类：有机化学品
S-BIOALLETHRIN 的 CAS 登记号为 22431-63-6。
分子式 C19H26O3，分子量 302.4。
别名/同义词：S-BIOALLETHRIN、Allethrins。
登记用途：Uses: Used in homes and gardens to kill flies and mosquitoes、The d-trans isomer is a more potent insecticide used to control animal parasites. Sold as mosquito coils、mats、oil formulations、and sprays、[EXTOXNET]、Farming (Pesticides) [Category: Industry]、For Allethrin、(the product that is a mixture)、(USEPA、OPP Pesticide Code: 004001) there are 0 labels match.、SRP: Not registered for current use in the U.S.、but approved pesticide uses may change periodically and so federal、state and local authorities must be consulted for currently approved uses.、Allethrin、For bioallethrin (USEPA、OPP Pesticide Code: 004003) ACTIVE products with label matches.、SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal、Bioallethrin、For S-bioallethrin (USEPA、OPP Pesticide Code: 004004) ACTIVE products with label matches.、S-Bioallethrin、For d-trans-allethrin (USEPA、d-trans-Allethrin、For more Uses (Complete) data for ALLETHRINS (14 total)、please visit the HSDB record page.、Use (kg、approx.) in Germany (2009): >10、Consumption (g per capita、approx.) in Germany (2009): 0.000122、Calculated removal (%): 92.4、Pyrethroids are used as insecticides. (L857)、Use Classification: INSECTICIDES、INSECTICIDES、Household Products: Information on 9 consumer products that contain d-trans-Allethrin in the following categories is provided:、• Inside the Home、• Pesticides、• Pet Care、Information on 21 consumer products that contain d-trans Allethrin in the following categories is provided:、• Personal Care、Information on 5 consumer products that contain d-cis、trans-Allethrin in the following categories is provided:、Methods of Manufacturing: Allethrin is prepared by the esterification of (1RS、3RS or cis、trans)-2、2-dimethyl-3-(2、2-dimethylvinyl) cyclopropanecarboxylic acid or chrysanthemic acid with (1RS)-3- allyl-2-methyl-4-oxocyclopent-2-ene-1-ol or allethrolone ... .、2-Allyl-3-methyl-2-cyclopenten-4-ol-1-one (allethrone) and chrysanthemum monocarboxlic anhydride in dibutyl ether at 150-175 °C for 3-6 hr are reacted. Upon cooling、the solution is diluted、the chrysanthemum moncarboxlic acid byproduct is removed by saponification、the organic phase is washed with water、and the solvent evaporated.、Formulations、Preparations: USEPA、OPP Pesticide Code: 004001、Trade Names: ENT 16275、ENT 17510、FDA 1446、FMC 249、NIA 249、Pyresin、Pynamin、Exthrin.、Aerosol dispenser、emulsifiable concentrate、dispersible powder、wettable powder、Coil、d-Allethrin is greater than、equal to 95% (1R)-isomers and greater than、equal to 75% trans isomers、Grades: 90% technical (approx 90% pure、with 10% of isomers or related cmpd)、20% technical、2.5% technical.、For more Formulations、Preparations (Complete) data for ALLETHRINS (268 total)、Consumption Patterns: Less than 30、000 lbs are marketed on average per year、Allethrins、General Manufacturing Information: Cyclopropanecarboxylic acid、2、2-dimethyl-3-(2-methyl-1-propen-1-yl)-、2-methyl-4-oxo-3-(2-propen-1-yl)-2-cyclopenten-1-yl ester: ACTIVE、The WHO Recommended Classification of Pesticides by Hazard identifies Allethrin (technical grade) as Class III: slightly hazardous、Main Use: insecticide.、The first pyrethroid pesticide、allethrin、was identified in 1949. Allethrin and other pyrethroids with a basic cyclopropane carboxylic ester structure are type I pyrethroids. ... All pyrethroids can exist as at least four stereoisomers、each with different biological activities. They are marketed as racemic mixtures or as single isomers. In commercial formulations、the activity of pyrethroids is usually enhanced by the addition of a synergist such as piperonyl butoxide、which inhibits metabolic degradation of the active ingredient.、ALLETHRIN IS ALLYL HOMOLOG OF CINERIN I、WHICH IS ONE OF THE CONSTITUENTS OF PYRETHRUM、OLDEST KNOWN INSECTICIDE.、Pyrethroids、are modern synthetic insecticides similar chemically to natural pyrethrins、but modified to increase stability in the natural environment.、For more General Manufacturing Information (Complete) data for ALLETHRINS (11 total)。
所属分类：Organic Chemicals。
S-BIOALLETHRIN（CAS 22431-63-6）的独立参考数据，整理自公开化学数据库。
| CAS 号 | 22431-63-6 |
|---|---|
| PubChem CID | 11442 |
| 分子式 | C19H26O3 |
| IUPAC 名称 | (2-methyl-4-oxo-3-prop-2-enylcyclopent-2-en-1-yl) 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate |
| UNII（FDA） | 0X03II877M |
| Molecular Weight | 302.4 |
|---|---|
| XLogP3 | 4.8 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 6 |
| Exact Mass | 302.18819469 |
| Monoisotopic Mass | 302.18819469 |
| Topological Polar Surface Area | 43.4 |
| Heavy Atom Count | 22 |
| Boiling Point | at 0.013kPa: 140 °C |
|---|---|
| Melting Point | ~4 °C |
| Flash Point | 130 °C |
| Flash Point | ~120 °C |
| LogP | 4.78 |
Allethrins; D-trans Allethrin; d-cis,trans-Allethrin; d-cis-trans-Allethrin; Allyl cinerin; HSDB 1511; PYNAMIN (JAPAN); RefChem:554622; PALLETHRINE (FRANCE); Pesticide Code: 004001; OMS 468; (RS)-Allethronyl (1R, cis)-chrysanthemate /d-cis-Allethrin/; (S)-Allethronyl (1R, trans)-chrysanthemate /S-Bioallethrin/; (RS)-Allethronyl (1R, cis, trans)-chrysanthemate /d-Allethrin/; (S)-Allethronyl (1R, cis, trans)-chrysanthemate /GZ1925000/; (RS)-Allethronyl (1R, trans) chrysanthemate /d-trans-Allethrin/ /Esbiothrin/
| 已通报的危害声明 | H302, H332, H400, H410, H312 (52.5%), H227, H317, H319 |
|---|
富右旋反式烯丙菊酯 · CAS 22431-63-6 · C19H26O3. UNII 0X03II877M. Boiling Point: at 0.013kPa: 140 °C; Melting Point: ~4 °C; Flash Point: 130 °C.
数据来源：PubChem / Wikidata；与随货 COA 不一致时以 COA 为准。
English page: S-BIOALLETHRIN