Name | Methylamino abamectin benzoate(salt) |
Synonyms | mk244 mk0244 Emamectin Benzoate EMAMECTIN-BENZOATE Emanectin Benzoate Emamectin Benzoate Solution, 1000ppm Methylamino abamectin benzoate(salt) (4''r)-4''-deoxy-4''-(methylamino)avermectin b1 benzoate (4''R)-4''-DEOXY-4''-(METHYLAMINO)AVERMECTIN B1 BENZOATE (4''R)-4''-Deoxy-4''-(methylamino)-avermectin B1 benzoate(salt) Avermectin B1, 4-deoxy-4-(methylamino)-, (4R)-, benzoate (salt) Avermectin b1, 4''-deoxy-4''-(methylamino)-, (4''R)-,benzoate (salt) 4''-deoxy-4''-(methylamino)-avermectinb(4''r)-avermectinbbenzoate(salt) (2aE,4E,5'S,6S,6'R,7S,8E,11R,13S,15S,17aR,20R,20aR,20bS)-20,20b-dihydroxy-5',6,8,19-tetramethyl-6'-[(1S)-1-methylpropyl]-17-oxo-5',6,6',10,11,14,15,17,17a,20,20a,20b-dodecahydro-2H,7H-spiro[11,15-methanofuro[4,3,2-pq][2,6]benzodioxacyclooctadecine-13,2'-pyran]-7-yl 2,6-dideoxy-3-O-methyl-4-O-[2,4,6-trideoxy-3-O-methyl-4-(methylammonio)-α-L-arabino-hexopyranosyl]-α-L-arabino-hexopyranoside benzoate |
CAS | 155569-91-8 137512-74-4 |
EINECS | 605-015-1 |
InChI | InChI=1/C49H75NO13.C7H6O2/c1-12-26(2)44-29(5)18-19-48(63-44)24-35-21-34(62-48)17-16-28(4)43(27(3)14-13-15-33-25-56-46-42(51)30(6)20-36(47(52)59-35)49(33,46)53)60-40-23-38(55-11)45(32(8)58-40)61-39-22-37(54-10)41(50-9)31(7)57-39;8-7(9)6-4-2-1-3-5-6/h13-16,18-20,26-27,29,31-32,34-46,50-51,53H,12,17,21-25H2,1-11H3;1-5H,(H,8,9)/b14-13+,28-16+,33-15+;/t26?,27-,29-,31-,32-,34+,35-,36-,37-,38-,39?,40?,41-,42+,43-,44+,45-,46+,48+,49+;/m0./s1 |
Molecular Formula | C49H77NO13 |
Molar Mass | 888.13 |
Melting Point | 141-146°C |
Appearance | neat |
Storage Condition | Inert atmosphere,Room Temperature |
MDL | MFCD01757274 |
Use | Widely used in vegetables, fruit trees, cotton and other crops on a variety of pest control |
Risk Codes | R25 - Toxic if swallowed R36 - Irritating to the eyes R50 - Very Toxic to aquatic organisms R57 - Toxic to bees R58 - May cause long-term adverse effects in the environment R36/37/38 - Irritating to eyes, respiratory system and skin. R50/53 - Very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment. R23 - Toxic by inhalation R21 - Harmful in contact with skin |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) S60 - This material and its container must be disposed of as hazardous waste. S61 - Avoid release to the environment. Refer to special instructions / safety data sheets. S36/37 - Wear suitable protective clothing and gloves. |
UN IDs | UN 2811 6.1/PG 3 |
WGK Germany | 3 |
RTECS | CL1203005 |
HS Code | 29224999 |
Raw Materials | Starch potato |
Reference Show more | 1. Zhang Zhenwei, Zhao Qingquan, Hao Xin, et al. Effects of abamectin and emamectin salt on virulence and detoxification enzyme activity of gypsy moth larvae. 2. [IF = 4.714] Xue Yin et al.Identification and pharmacological characterization of histamine-gated chloride channels in the fall armyworm, Spodoptera frugiperda.Insect Biochem Molec. 2022 Jan;140:103698 |
is the result of the American Merk 8 Co. Company in a-l 4 of avermectin 4 '-one (2,-Oleanolic sugar)-a-l-Oleanolic sugar on the hydroxyl group derivatization study, from the fermentation product of avermectin Bl synthesis.
is a new type of high activity broad-spectrum microbial insecticide, which is the product of chemical modification of abamectin. The efficacy of lepidopteran pests is significantly higher than that of abamectin. The results showed that the activity of emamectin to Diamondback moth and beet armyworm was more than 10 times that of abamectin, and its contact toxicity to cotton bollworm was 146.7 times that of beta-cypermethrin, the gastric toxic activity against cotton bollworm is 4721 times that of methyl parathion. The control effect of 6000 times dilution of 1% emamectin EC was equivalent to that of 4.5% times dilution of 1667 beta-cypermethrin EC, and its activity on Chilo suppressalis was higher than that of abamectin.
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
introduction | research progress on resistance mechanism of emamectin benzoate emamectin benzoate (emamectin benzoate), abbreviated as emamectin salt, is the result of derivatization of hydroxyl groups on 4 "-(α-1-Oleanosyl)-α-1 Oleanosaccharide by Merck Company in 1984. As a new type of antibiotic biological insecticide, emamectin salt has the advantages of broad spectrum, high efficiency, low toxicity and low residue, and has good insecticidal effect on lepidopteran pests. |
properties | the original drug is white or light yellow crystalline powder; Melting point: 141-146 ℃; Soluble in acetone and methanol, slightly soluble in water, insoluble in hexane. Stability: Stable under normal storage conditions. |
use | emamectin salt, as a new type of antibiotic biogenic insecticide, has the advantages of broad spectrum, high efficiency, low toxicity and low residue, and has good insecticidal effect on lepidopteran pests. the LC90 value of emamectin salt on some lepidopteran insects ranges from 0.002 mg/L to 0.89 mg/L. Compared with the lead compound avermectin, emamectin salt has lower toxicity, and its toxicity to rats is only 1/6 of avermectin. It is safe for humans and animals under conventional doses and is easy to degrade. At present, emamectin/abamectin is often used to control vegetable pests, such as Plutella xylostella, Spodoptera exigua, Spodoptera litura, etc. Because of its good control effect, it is widely used in the control of cruciferous vegetable pests and effectively controls the occurrence scale of lepidopteran pest population, and delays the evolution of its resistance to traditional pesticides. It is widely used to control various pests on vegetables, fruit trees, cotton and other crops Insecticides and acaricides. |
mechanism of action | emamectin benzoate is a low-toxic insecticide and acaricide of microbial origin. it is a highly efficient biological agent synthesized on the basis of abamectin. it has the characteristics of high activity, wide insecticidal spectrum, good miscibility, long duration of effect, safe use, etc., and its mode of action is mainly stomach poison and has contact killing effect. Its insecticidal mechanism is to hinder the pest's motor nerves. Do not use in fish ponds, bee farms, mulberry fields and their surroundings, and do not pollute waters such as ponds. It is poisonous to bees and should not be used during the flowering period of fruit trees. The safe harvest interval for general crops is 7 days. |
toxicity | toxicity and poisoning symptoms: the original drug is highly toxic, and the preparation is low toxic (nearly non-toxic); The early symptoms after poisoning are pupil dilation, movement disorder, muscle tremor, and vomiting in severe cases. treatment of poisoning: oral: immediately induce vomiting and give patients ipecac syrup or ephedrine, but do not induce vomiting or pour anything into coma patients. Avoid the use of drugs that enhance the activity of gamma-aminobutyric acid (GABA) during rescue. Such as (barbiturate, valproic acid, etc.). The stomach can be lavaged when swallowed in large quantities. |