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Milbemycin D

Base Information Edit
  • Chemical Name:Milbemycin D
  • CAS No.:77855-81-3
  • Molecular Formula:C33H48O7
  • Molecular Weight:556.74
  • Hs Code.:
  • UNII:04S0E2XJQI
  • Wikidata:Q27247671
  • Mol file:77855-81-3.mol
Milbemycin D

Synonyms:5-hydroxymilbemycin beta7;CL 301,423;CL 301423;Cydectin;Milbeknock;milbemectin;milbemycin A3;milbemycin A4;milbemycin alpha1;milbemycin alpha10;milbemycin alpha11;milbemycin alpha13;milbemycin alpha14;milbemycin alpha15;milbemycin alpha2;milbemycin alpha3;milbemycin alpha4;milbemycin alpha5;milbemycin alpha6;milbemycin alpha7;milbemycin alpha8;milbemycin alpha9;milbemycin B;milbemycin beta1;milbemycin beta12;milbemycin beta2;milbemycin beta3;milbemycin D;milbemycins;mixture of milbemycins A3 and A4;moxidectin

Suppliers and Price of Milbemycin D
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Usbiological
  • Milbemycin D
  • 1mg
  • $ 593.00
  • TRC
  • MilbemycinD
  • 0.5mg
  • $ 435.00
  • Cayman Chemical
  • Milbemycin D ≥95%
  • 5mg
  • $ 1196.00
  • Cayman Chemical
  • Milbemycin D ≥95%
  • 1mg
  • $ 319.00
  • American Custom Chemicals Corporation
  • MILBEMYCIN D 95.00%
  • 5MG
  • $ 502.15
Total 12 raw suppliers
Chemical Property of Milbemycin D Edit
Chemical Property:
  • Vapor Pressure:5.55E-25mmHg at 25°C 
  • Melting Point:186-188° 
  • Refractive Index:1.5300 (estimate) 
  • Boiling Point:735.7°C at 760 mmHg 
  • Flash Point:231.9°C 
  • PSA:94.45000 
  • Density:1.18g/cm3 
  • LogP:5.17030 
  • Storage Temp.:Hygroscopic, -20°C Freezer, Under inert atmosphere 
  • Solubility.:Chloroform (Slightly) 
  • XLogP3:4.1
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:1
  • Exact Mass:556.34000387
  • Heavy Atom Count:40
  • Complexity:1090
Purity/Quality:

98%Min *data from raw suppliers

Milbemycin D *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1CCC2(CC3CC(O2)CC=C(CC(C=CC=C4COC5C4(C(C=C(C5O)C)C(=O)O3)O)C)C)OC1C(C)C
  • Isomeric SMILES:C[C@H]1CC[C@]2(C[C@@H]3C[C@H](O2)C/C=C(/C[C@H](/C=C/C=C/4\CO[C@H]5[C@@]4([C@@H](C=C([C@H]5O)C)C(=O)O3)O)C)\C)O[C@@H]1C(C)C
  • Uses Milbemycins are a complex family of macrocyclic lactones containing a highly characteristic spiroketal group, produced by Streptomyces hydroscopicus subsp. aureolarcrimosus. Milbemycin D is a minor member of a group of analogues containing a 25-isopropyl substituent. Milbemycin D is a highly selective and potent nematocide and insecticide. Like the closely related avermectin, milbemycins are thought to act on chloride-gated ion channels. Milbemycin D (Milbemycin EP Impurity C) is a macrocyclic lactones that can be used as a nematocide and insecticide.
Technology Process of Milbemycin D

There total 17 articles about Milbemycin D which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With sodium tetrahydroborate; In methanol; at 0 ℃; for 0.166667h;
DOI:10.1021/ja961071u
Guidance literature:
Multi-step reaction with 6 steps
1: 79 percent / Pr4NRuO4, NMO, 4 Angstroem molecular sieves / CH2Cl2 / 4 h / Ambient temperature
2: Et3N / CH2Cl2 / 8 h / 0 °C
3: 0.023 g / CH2Cl2 / 1 h / -78 °C
4: 66 percent / aq. 48percent HF, pyridine / acetonitrile / 24 h / Ambient temperature
5: NaIO4 / tetrahydrofuran; H2O / 2 h / Ambient temperature
6: 32 percent / NaBH4 / methanol / 0.17 h / 0 °C
With pyridine; sodium tetrahydroborate; sodium periodate; N-methyl-2-indolinone; tetrapropylammonium perruthennate; 4 A molecular sieve; hydrogen fluoride; triethylamine; In tetrahydrofuran; methanol; dichloromethane; water; acetonitrile;
DOI:10.1021/ja961071u
Guidance literature:
Multi-step reaction with 5 steps
1: Et3N / CH2Cl2 / 8 h / 0 °C
2: 0.023 g / CH2Cl2 / 1 h / -78 °C
3: 66 percent / aq. 48percent HF, pyridine / acetonitrile / 24 h / Ambient temperature
4: NaIO4 / tetrahydrofuran; H2O / 2 h / Ambient temperature
5: 32 percent / NaBH4 / methanol / 0.17 h / 0 °C
With pyridine; sodium tetrahydroborate; sodium periodate; hydrogen fluoride; triethylamine; In tetrahydrofuran; methanol; dichloromethane; water; acetonitrile;
DOI:10.1021/ja961071u
Refernces Edit
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