TIANFU-CHEM - Mupirocin CAS NO.12650-69-0

Min.Order Quantity:: 1 Kilogram

Purity:: 98%

Port:: Shanghai

Payment Terms:: L/C,D/A,D/P,T/T,MoneyGram,Other

Add to Inquiry Cart

Product Details

Keywords

Mupirocin
12650-69-0
C26H44O9

Quick Details

ProName: TIANFU-CHEM - Mupirocin
CasNo: 12650-69-0
Molecular Formula: C26H44O9
Appearance: White Crystalline Solid
Application: Organic synthesis
DeliveryTime: Prompt
PackAge: IN 25kg drums
Port: Shanghai
ProductionCapacity: 10 Metric Ton/Month
Purity: 98%
Storage: room tempurature
Transportation: As per the MSDS
LimitNum: 1 Kilogram
Heavy metal: N/A
Grade: Industrial Grade,Food Grade,Pharma Gra...
N/A: N/A

Superiority

our company engages in sodium tripolyphosphate (stpp) and sodium hexametabphosphate (shmp) production; development of noble metal catalysts, synthesis of electronic chemical materials and general chemicals imp&exp trading business. the company is located in zhengzhou high-tech development zone with import and export license. we passed iso 9001:2008 in 2009, and won "high-tech enterprise" by provincial government in 2013. our stpp and shmp has reached an annual output of 30000 tons and has successfully passed sgs, ciq audits on many occasions.

in 2011 we entered the fine chemical market of noble metal catalyst ,organic phosphine ligands and oled intermediates.with the joint efforts of our senior experts and professional technicians, tianfu has developed more than 500 compounds, which are widely used in the fields of production and life science. the objective of the company is to put quality first and put our customer’s needs first - the satisfaction of our customers is the company's ultimate goal. improving product quality and service level is our responsibility, and creating more value for our customer’s is our purpose. we are constantly striving to make henan tianfu a leading chemical supplier, and hope to create a better future with you.

Details

mupirocin basic information

topical antibiotics adverse reactions precautions chemical properties application production methods

product name:	mupirocin
synonyms:	mupirocin;mupirocin calcium;pseudomonic acid;pseudomonic acid a;(2s-(2-alpha(e;4-beta,5-alpha(2r,3r(1r,2r))))-3-beta;bactroban;nonanoicacid,9((3-methyl-1-oxo-4-(tetrahydro-3,4-dihydroxy-5-((3-(2-hydroxy-1
cas:	12650-69-0
mf:	c26h44o9
mw:	500.62
einecs:	231-791-2
product categories:	active pharmaceutical ingredients;intermediates & fine chemicals;pharmaceuticals;chiral reagents;heterocycles;api;inhibitors
mol file:	12650-69-0.mol

mupirocin chemical properties

mp	77-780c
storage temp.	-20°c freezer, under inert atmosphere
solubility	h₂o: 12 mg/ml, soluble
form	solid
cas database reference	12650-69-0(cas database reference)

safety information

wgk germany	2
rtecs	ra6907000

msds information

provider	language
5,9-anhydro-2,3,4,8-tetradeoxy-8-[[3-(2-hydroxy-1-methylpropyl)oxiranyl]methyl]-3-methyl-[2e,8[2s,3s(1s,2s)]]-l-talonon-2-enonic acid 8-carboxyoctyl ester	english
sigmaaldrich	english

mupirocin usage and synthesis

topical antibiotics	the crude drug of bactroban ointment produced by the well-known domestic pharmaceutical company smithkline is mupirocin which is a new type of local topical antibiotic and a kind of metabolic substance produced in the culture solution of pseudomonas fluorescence, that is, pseudomonas a. mainly through reversibly combined with isoleucine transfer rna synthetase, this product can prevent the isoleucine incorporation and terminate the protein synthesis in cells containing isoleucine, leading to bacterial death. at low concentrations, this product has the inhibitory effect and at high concentrations, it has the bactericidal effect. this product is highly sensitive to a variety of gram-positive bacteria associated with skin infections, particularly staphylococcus aureus (including drug-resistant staphylococcus aureus) and streptococcus pyogenes; and it is also available for listeria monocytogenes and erythema erysipelothrix bacteria; it is generally not sensitive to gram-negative bacteria, but have some antibacterial effect on some gram-negative bacteria such as e. coli, neisseria, haemophilus influenzae and neisseria gonorrhoeae and is not sensitive to the majority of anaerobic bacteria and the normal flora of the skin and has low efficacy against fungi. rate of occurrence is very low in vitro resistant mutants. after applied into the skin, this medicine can penetrate into the stratum corneum, but the absorption rate is very low. the binding rate of this drug and human serum protein is 95%. when absorbed, it is rapidly metabolized to an inactive substance single spore acid (monic acid) and excreted by the kidneys. the minimum inhibitory concentration of most sensitive staphylococcus is 0.01 ~ 0.25mg / l, that of sensitive streptococcus is 0.06 ~ 0.5mg / l, and that of listeriosis is 8mg / l. this product is more effective in vitro tests under acidic conditions than that under alkaline conditions. when human serum exists, activity of this drug reduce to 1/10 ~ 1/20. currently, in china, mupirocin is mainly and clinically used for the treatment of staphylococcus aureus and streptococcus caused by various infectious skin diseases: primary skin infections such as impetigo, folliculitis, and boils carbuncles etc; secondary skin infections such as eczema, atopic dermatitis, skin ulcers, surgical wounds, small burns, skin trauma; and other prevent infections such as small wounds, wound infections, and other sterilization venereal damage.
adverse reactions	topical application of this drug is generally no adverse reactions, occasionally with skin burning sensation, stinging sensation, aminotransferase rising, itching, dryness and erythema. its occurrence rate is very low(3%) with a lesser degree. the medicine is generally tolerated and without being stopped. for long-term use, this drug may result in overgrowth of non-susceptible strains; nasal agent can cause headache, taste disturbance, rhinitis, pharyngitis, and other respiratory disorders. the above information is edited by the chemiclbook of bai linlin.
precautions	1. allergies of pseudomonas acid or polyethylene glycol are disabled to use; patients who suffer from moderate or severe renal impairment use it with caution; the impact on pregnant or lactating women are not clear, temporarily not available. 2. ointments made from polyethylene glycol which is used as a substrate, is only available for a small area of skin bacterial infection, and cannot be used to extensive burns or wounds so as to prevent the renal damage due to the absorption of polyethylene glycol, as well as mucous membranes, for example, used in the eyes and noses. as with nasal staph infections, the use of ointment base should be replaced by vaseline. 3. although mupirocin toxicity is low, we should avoid the abuse or the use of the drug for a long term in case of generating drug-resistant strains.
chemical properties	this medicine can be obtained from crystallized ether, and its melting point is 77 ~ 78 ℃. [α]d20-19.3°(c = 1, methanol). the maximum absorption of uv (ethanol): 222nm(ε14500).
application	topical antibiotics. this product is generally used for the inflammation of the skin, eczema, etc., or made into mupirocin ointment in the market.by reversibly binding to isoleucine transfer rna synthetase, this product can prevent isoleucine incorporated so that the synthesis of all proteins in cells containing isoleucine can be stopped.
production methods	it is a kind of substance produced by the pseudomonas fluorescence, including pseudomonic acids a, b, c, d. mupirocin is pseudomonic acid a which is the major metabolite.
chemical properties	white crystalline solid
usage	antibacterial, antimycoplasmal, isoleucyl-trna synthetase inhibitor
usage	mupirocin, is a major component of the pseudomonic acid, an antibiotic complex produced by pseudomonas fluorescens ncib 10586. topical antibacterial.
usage	pseudomonic acid is a potent antibiotic produced by pseudomonas fluorescens, reported by fuller et al. in 1971. pseudomonic acid has broad spectrum activity against gram positive bacteria and was approved for topical human use in 1985. pseudomonic acid acts as a potent and selective inhibitor of isoleucyl-trna synthetase.
usage	vasodilator
usage	an antibiotic inhibitor of isoleucyl-trna synthetase