Emamectin

Title: Emamectin
CAS Registry Number: 137335-79-6; 121124-29-6 (major component); 121424-52-0 (minor component)
Additional Names: (4¢¢R)-5-O-demethyl-4¢¢-deoxy-4¢¢-(methylamino)avermectin A1a and (4¢¢R)-5-O-demethyl-25-de(1-methylpropyl)-4¢¢-deoxy-4¢¢-(methylamino)-25-(1-methylethyl)avermectin A1a (9:1)
Literature References: Mixture of semi-synthetic avermectins, q.v., consisting (9:1) of 4¢¢-epi-(methylamino)-4¢¢-deoxyavermectin B1a, (C49H75NO13) and 4¢¢-epi-(methylamino)-4¢¢-deoxyavermectin B1b, (C48H73NO13). Prepn: H. Mrozik, US 4874749 (1989 to Merck & Co.); and insecticidal activity: H. Mrozik et al., Experientia 45, 315 (1989). Synthesis: R. J. Cvetovich et al., J. Org. Chem. 59, 7704 (1994). Avian toxicity studies: A. C. Chukwudebe et al., Environ. Toxicol. Chem. 17, 1118 (1998). Review: M. H. Fisher, ACS Symp. Ser. 524, 169-182 (1993); H. Mrozik, ibid. 551, 54-73 (1994).
Properties: LC50 (48 hr) in Daphnia magna: 2.9 mg/l; LC50 in rainbow trout, bluegill sunfish (mg/l) at 24 hrs: >1.0, 0.75; at 48 hrs: >1.0, 0.45; at 96 hrs: 0.67, 0.24 (Mrozik, US 4874749).
Toxicity data: LC50 (48 hr) in Daphnia magna: 2.9 mg/l; LC50 in rainbow trout, bluegill sunfish (mg/l) at 24 hrs: >1.0, 0.75; at 48 hrs: >1.0, 0.45; at 96 hrs: 0.67, 0.24 (Mrozik, US 4874749)
Derivative Type: Benzoate
CAS Registry Number: 137512-74-4
Additional Names: 4¢¢-Deoxy-4¢¢-epi-N-methylaminoavermectin B1 benzoate
Manufacturers' Codes: MK-244
Trademarks: Affirm (Novartis); Proclaim (Syngenta); Slice (Schering-Plough)
Properties: Exists as the anhydrous and various hydrated forms having different crystal morphologies. Amt of water is nonstoichiometric. 1.1% form is an off white crystalline powder, mp 141-146°. [a]D -6.9° (c = 0.5% in methanol). uv max (10% methanol in water by volume): 244 nm (A11% = 327 corr). log P (n-octanol/aq phosphate): 3.0 (pH 5.1); 5.0 (pH 7.0). pKa 4.2; 7.6. Soly 0.32 mg/ml at pH 5 (aq); 0.024 mg/ml at pH 7 (aq). Freely sol in chloroform and methanol. Insol in hexane. LD50 in mallard ducks, northern bobwhite quail (mg/kg): 76, 264 orally (Chukwudebe).
Melting point: mp 141-146°
pKa: pKa 4.2; 7.6
Optical Rotation: [a]D -6.9° (c = 0.5% in methanol)
Log P: log P (n-octanol/aq phosphate): 3.0 (pH 5.1); 5.0 (pH 7.0)
Absorption maximum: uv max (10% methanol in water by volume): 244 nm (A11% = 327 corr)
Toxicity data: LD50 in mallard ducks, northern bobwhite quail (mg/kg): 76, 264 orally (Chukwudebe)
Use: Insecticide.
Embelin Embramine Emepronium Bromide Emetine Emitefur

Emamectin
Emamectins.png
Identifiers
CAS number 119791-41-2 YesY, 155569-91-8 (Benzoate) YesY
UNII 8C43B81H4W YesY
RTECS number CL1203005
ATCvet code QP54AA06
Jmol-3D images Image 1
Properties
Molecular formula C49H75NO13
Molar mass 886.12 g mol−1
Appearance White or faintly yellow powder
Melting point 141 to 146 °C; 286 to 295 °F; 414 to 419 K
Solubility in water 30-50 ppm (pH 7)
Hazards
R-phrases R25 R36 R50 R57 R58
S-phrases S26 S36 S45 S60 S61
NFPA 704
NFPA 704.svg
2
2
0
 YesY (verify) (what is: YesY/N?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Infobox references

Emamectin is the 4”-deoxy-4”-methylamino derivative of abamectin, a 16-membered macrycyclic lactone produced by the fermentation of the soil actinomycete Streptomyces avermitilis.[1][2] It is generally prepared at the salt with benzoic acid, emamectin benzoate, which is a white or faintly yellow powder.[3] Emamectin is widely used in the US and Canada as an insecticide because of its chloride channel activation properties.[4]