MILBEMECTIN

MILBEMECTIN Suppliers list
Company Name: BOC Sciences
Tel: +16314854226
Email: inquiry@bocsci.com
Products Intro: Product Name:Milbemectin
Purity:>95% by HPLC Remarks:BOC Sciences also provides custom synthesis services for Milbemectin.
Company Name: Lynnchem  
Tel: 86-(0)29-85992781 17792393971
Email: info@lynnchem.com
Products Intro: Product Name:MILBEMECTIN
Purity:>95% by HPLC Package:1mg;5mg
Company Name: Novachemistry  
Tel: 44-20819178-90 02081917890
Email: info@novachemistry.com
Products Intro: Product Name:Milbemectin
Purity:>95% by HPLC Package:1mg;5mg
Company Name: ChemeGen(Shanghai) Biotechnology Co.,Ltd.  
Tel: 18818260767
Email: sales@chemegen.com
Products Intro: Product Name:Milbemectin
Purity:98% Package:10 mg;50 mg;100 mg;500 mg;1 g;5 g;10 g
Company Name: Wako Pure Chemical Industries, Ltd.  
Tel: +81 6 6203 3741
Email: labchem-tec@wako-chem.co.jp
Products Intro:
MILBEMECTIN Basic information
Product Name:MILBEMECTIN
Synonyms:MILBEMECTIN
CAS:
MF:C63H90O14
MW:1071.38
EINECS:
Product Categories:
Mol File:Mol File
MILBEMECTIN Structure
MILBEMECTIN Chemical Properties
vapor pressure <1.3 x 10-8 Pa (20 °C)
Water Solubility Milbemectin A3: 7.2 mg l-1
Milbemectin A4: 0.88 mg l-1 at 20 °C
Safety Information
MSDS Information
MILBEMECTIN Usage And Synthesis
UsesMilbemectin is a mixture of milbemectin A3 (30%) and milbemectin A4 (70%). It is an active acaricide, produced from fermentation products of soil microorganisms Streptomyces hygroscopicus subsp. Aureo- lacrirnosus. Milbemectin is highly active on various phytophagous mites on tea, pome fruits, stone fruits, citrus, watermelon, strawberry and egg plants. It is also an insecticide active against aphid, cutworm, leafroller and thrips.
UsesMilbemectin is a mixture of the two most abundant milbemycin analogues, A3 and A4, produced by Streptomyces hydroscopicus subsp. aureolarcrimosus. Originally defined as a mixture of 30% milbemycin A3 and 70% milbemycin A4, our product is specifically blended to meet this specification. Milbemectin is a highly selective and potent insecticide and acaricide used as an agri-chemical for crop protection.
Metabolic pathwayLimited information is available on the environmental fate and metabolism of the milbemectins. Aolu et al. (1994) reported the ready oxidative degradation of milbemectins in the environment. Minimal root uptake by plants occurs and milbemectin dissipates rapidly on plant foliage (DT50 ca. 1 day). Hydroxylation is the primary metabolic reaction of milbemectins in laboratory animals.
MILBEMECTIN Preparation Products And Raw materials
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