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carbomycin

CAS No.
4564-87-8
Chemical Name:
carbomycin
Synonyms
M 4209;Nsc51001;NSC 55924;MagnaMycin;Aids012086;carbomycin;Aids-012086;Magnamycin a;CarboMycin A;DeltaMycin A4
CBNumber:
CB41380701
Molecular Formula:
C42H67NO16
Molecular Weight:
841.98
MDL Number:
MFCD01716264
MOL File:
4564-87-8.mol

carbomycin Properties

Melting point 214°
alpha D25 -58.6° (chloroform)
Boiling point 769.45°C (rough estimate)
Density 1.1761 (rough estimate)
refractive index 1.6220 (estimate)
pka pKb 7.2(at 25℃)
FDA 21 CFR 556.110
FDA UNII 3952621T3O

SAFETY

Risk and Safety Statements

Toxicity LD50 i.v. in mice: 550 mg/kg (Tanner)

carbomycin price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation API0010936 CARBOMYCIN 95.00% 4564-87-8 5MG $385 2021-12-16 Buy
American Custom Chemicals Corporation API0010936 CARBOMYCIN 95.00% 4564-87-8 50MG $2194.5 2021-12-16 Buy
Product number Packaging Price Buy
API0010936 5MG $385 Buy
API0010936 50MG $2194.5 Buy

carbomycin Chemical Properties,Uses,Production

Originator

Magnamycin,Pfizer,US,1953

Uses

Sixteen-membered-ring macrolite antibiotic complex similar to Leucomycin and Erythromycin, produced by Stroptomyces halstedii.

Definition

An antibiotic isolated from products of Strepto- myces halstedii when grown in suitable media by the deep-culture method. It inhibits growth of certain gram-positive bacteria such as staphylo- cocci, pneumococci, and hemolytic streptococci.

Manufacturing Process

A selected strain of Streptomyces halstedii was cultivated in an aqueous nutrient medium under aerobic conditions and the resulting broth containing carbomycin antibiotics was filtered. The solutions was extracted twice at pH 6.5 with one-quarter volume of methyl isobutyl ketone. The combined extracts were concentrated to one-tenth volume under vacuum, and the antibiotics were extracted into water adjusted to a pH of about 2 with sulfuric acid. After adjusting the separated aqueous solution to pH 6.5, the antibiotic was extracted into benzene and the solution was concentrated to a small volume. Addition of hexane resulted in the separation of a solid product containing the benzene complexes of carbomycin A and carbomycin B, present in the fermentation broth.

brand name

Magnamycin (Pfizer).

Therapeutic Function

Antibiotic

Safety Profile

Poison by subcutaneous route. Moderately toxic by intravenous and intramuscular routes. When heated to decomposition it emits toxic fumes of NOx.

carbomycin Preparation Products And Raw materials

Raw materials

Preparation Products

carbomycin Suppliers

Global( 17)Suppliers
Supplier Tel Email Country ProdList Advantage
TargetMol Chemicals Inc.
support@targetmol.com United States 38663 58
Shaanxi Cuikang Pharmaceutical Technology Co., Ltd
+8618791163155 18791163155@163.com China 3558 58
J & K SCIENTIFIC LTD. 18210857532 18210857532 jk.info@jkchemical.com China 96815 76
Chemsky (shanghai) International Co.,Ltd 021-50135380 shchemsky@sina.com China 15402 60
BOC Sciences 1-631-485-4226; 16314854226 info@bocsci.com United States 12952 65
Shenzhen Polymeri Biochemical Technology Co., Ltd. +86-400-002-6226 +86-13028896684; sales@rrkchem.com China 57422 58
Energy Chemical 021-58432009 400-005-6266 marketing@energy-chemical.com China 44918 58
Merck KGaA 21-20338288 ordercn@merckgroup.com China 292394 58
Biosynth Biological Technology (Suzhou) Co Ltd 51288865780 sales@biosynth.com China 233051 58
carbomycin 3-Methyl-butyric acid 6-{[(Z)-7-acetoxy-8-methoxy-3,12-dimethyl-5,13-dioxo-10-(2-oxo-ethyl)-4,17-dioxa-bicyclo[14.1.0]heptadec-14-en-9-yloxy]-dimethylamino-hydroxy-methyl-tetrahydro-pyran-3-yloxy}-4-hydroxy-2,4-dimethyl-tetrahydro-pyran-3-yl ester Aids012086 Aids-012086 Magnamycin a Nsc51001 (12S,13S)-9-Deoxy-12,13-epoxy-12,13-dihydro-9-oxoleucoMycin V 3-Acetate 4B-(3-Methylbutanoate) CarboMycin A DeltaMycin A4 M 4209 MagnaMycin NSC 55924 Leucomycin V, 9-deoxy-12,13-epoxy-12,13-dihydro-9-oxo-, 3-acetate 4B-(3-methylbutanoate), (12S,13S)- Carbomycin DISCONTINUED 4564-87-8 C42H67NO16 Amines Chiral Reagents Heterocycles Intermediates & Fine Chemicals Pharmaceuticals