ChemicalBook > CAS DataBase List > Avilamycin

Avilamycin

Product Name
Avilamycin
CAS No.
11051-71-1
Chemical Name
Avilamycin
Synonyms
Avilomycin;AvilamycinQ: What is Avilamycin Q: What is the CAS Number of Avilamycin Q: What is the storage condition of Avilamycin Q: What are the applications of Avilamycin
CBNumber
CB81104189
Molecular Formula
C61H88Cl2O32
Formula Weight
1404.23822
MOL File
11051-71-1.mol
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Avilamycin Property

Melting point:
188-189℃
alpha 
D20 +0.8° (c = 1.165 in abs ethanol) and -7.7° (c = 1.083 in chloroform)
solubility 
Acetone (Slightly), DMSO (Slightly)
form 
Solid
color 
Light Beige to Light Brown
Stability:
Hygroscopic
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Safety

Hazardous Substances Data
11051-71-1(Hazardous Substances Data)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H319Causes serious eye irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TRC
Product number
A794655
Product name
Avilamycin(~80%)
Packaging
50mg
Price
$90
Updated
2021/12/16
TRC
Product number
A794655
Product name
Avilamycin(~80%)
Packaging
250mg
Price
$345
Updated
2021/12/16
TRC
Product number
A794655
Product name
Avilamycin(~80%)
Packaging
1g
Price
$1130
Updated
2021/12/16
Biosynth Carbosynth
Product number
FA74919
Product name
Avilamycin
Packaging
1mg
Price
$50
Updated
2021/12/16
Biosynth Carbosynth
Product number
FA74919
Product name
Avilamycin
Packaging
2mg
Price
$80
Updated
2021/12/16
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Avilamycin Chemical Properties,Usage,Production

Originator

Maxus,Eli Lilly

Uses

Antibacterial.

Manufacturing Process

Avilamycin is produced from Streptomyces viridochromogenes NRRL 2860:
A nutrient solution is prepared which contains 20.0 g of meat meal, 20.0 g of salt extract, 10.0 g of calcium carbonate and 1 L of tap water and adjusted to pH=7. This solution, or a multiple thereof, is charged into conical flasks of 500 ml capacity (100 ml of nutrient solution each) or into fermenters of 500 L capacity (300 L of nutrient solution each) and sterilized for 20-30 min under a pressure of 1 atm. The contents of the flasks are then inoculated with up to 10% of a partially sporulating vegetative culture of Streptomyces viridochromogenes NRRL 2860 and incubated at 27°C with thorough shaking or stirring, and in the fermenters with aerating with about 1 volume of sterile air per volume of nutrient solution per minute. The cultures are allowed to grow for 24-48 h, mixed with about 1.5% of a filtration assistant and then filtered depending on the volume, through a suction filter or a filter press or a rotary filter to free the antibiotically active aqueous solution from the mycelium and other solid constituents.
The medium described above is replaced the nutrient media: 10.0 g of crude glucose, 5.0 g of peptone, 3.0 g of meat extract (Oxo Lab- Lemco), 5.0 g of sodium chloride, 10.0 g of calcium carbonate and 1 L of tap water, pH - prior to sterilization: 7.5, analogous sterilization, inoculation with Streptomnyces viridochromogenes NRRL 2860, incubation at 27°C and filtration likewise yield aqueous antibiotically active solutions.
90 L of culture filtrate are extracted with 20 L of ethyl acetate, and the extract is concentrated to 400 ml. When the concentrate is kept for 20 h at 2°C, avilamycin precipitates in the form of a dense floccular substance which is filtered off. After having been dried in an exsiccator, the practically colorless crystal cake consisting of strongly felted small needles weighs 3.07 g. The mother liquors are concentrated to about 200 ml and mixed with twice the amount of ether. When the concentrate is kept for 4 days at 0°C, a further 3.28 g of avilamycin crystallize out. 3.0 g of the crystallizate are dissolved in 50 ml of acetone, and a small amount of insoluble sludge is filtered off. The clear filtrate is mixed with ether and concentrated. On cooling, 2.0 g of colorless fine needles crystallize out. Concentration of the mother liquors to about one quarter their volume produces a further 0.48 g of crystals. For analysis a test portion of these crystals is recrystallized 4 times from acetone+ether and dried for 20 h in a high vacuum at 70°C. The analytically pure antibiotic avilamycin have a melting point 188°-189.5°C. Optical rotation [α]D 20=+0.8° (c=1.165 in absolute ethanol).

brand name

Surmax (Lilly).

Therapeutic Function

Antibiotic

Avilamycin Preparation Products And Raw materials

Raw materials

Preparation Products

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Avilamycin Suppliers

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View Lastest Price from Avilamycin manufacturers

WUHAN FORTUNA CHEMICAL CO., LTD
Product
Avilamycin 11051-71-1
Price
US $0.00/KG
Min. Order
1KG
Purity
98%min
Supply Ability
30tons/month
Release date
2023-01-12
HebeiShuoshengImportandExportco.,Ltd
Product
Avilamycin 11051-71-1
Price
US $6.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
2000KG/Month
Release date
2024-08-05
Hebei Zhuanglai Chemical Trading Co Ltd
Product
Avilamycin 11051-71-1
Price
US $150.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
500kg
Release date
2024-12-24

11051-71-1, AvilamycinRelated Search:


  • Avilomycin
  • AvilamycinQ: What is Avilamycin Q: What is the CAS Number of Avilamycin Q: What is the storage condition of Avilamycin Q: What are the applications of Avilamycin
  • 11051-71-1
  • C61H90Cl2O32