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CasNo: 100986-85-4
Molecular Formula: C18H20FN3O4
Appearance: Slight yellow powder
99% Purity Commercial production Levofloxacin hydrochloride 100986-85-4 with Cheapest Price We supply high quality Levofloxacin hydrochloride (CAS 100986-85-4), in stock, factory directly supply to clients, lower prices, more competitiveness.
Levofloxacin hydrochloride is Slight yellow powder, while it's Molecular Formula is C18H20FN3O4. Antibacterial.
The CAS number of Levofloxacin hydrochloride is 100986-85-4.
More information of Levofloxacin hydrochloride 100986-85-4 are:
Synonyms |
Elequine;(-)-Ofloxacin;7H-Pyrido[1,2,3-de]-1,4-benzoxazine-6- carboxylic acid,9-fluoro-2,3-dihydro-3- methyl-10-(4-methyl-1-piperazinyl)-7-oxo-,(3S)-;Levaquin (TN);Levofloxacino [INN-Spanish];Levofloxacin (JAN/USAN);Levaquin;Levofloxacin [USAN:INN:JAN];Levofloxacine [INN-French];(S)-Ofloxacin;Ofloxacin S-(-)-form;Iquix;(S)-9-Fluoro-2,3-dihydro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-7H-pyrido(1,2,3-de)-1,4-benzoxazine-6-carboxylic acid;Levofloxacinum [INN-Latin];7H-Pyrido(1,2,3-de)-1,4-benzoxazine-6-carboxylic acid, 2,3-dihydro-9-fluoro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-, (S)-;(S)-(-)-Ofloxacin;8-fluoro-3-methyl-9-(4-methyl-piperazin-1-yl)-6-oxo-2,3-dihydro-6H-1-oxa-3a-aza-phenalene-5-carboxylic acid;Levoflaoxacin;Levofloxacincas; |
CAS Number |
100986-85-4 |
Molecular Formula |
C18H20FN3O4 |
Molecular Weight |
361.373 |
Density |
1.48 g/cm3 |
Melting Point |
218 °C |
Boiling Point |
571.495 °C at 760 mmHg |
Flash Point |
299.43 °C |
HS CODE |
29349990 |
PSA |
75.01000 |
LogP |
1.54690 |
Pka |
5.19±0.40(Predicted) |
Levofloxacin, the optically active S-isomer of the fluoroquinolone antibiotic ofloxacin, is two to four times more potent than ofloxacin with reportedly less side effects in treating infections of the lower respiratory and urinary tract, prostate infections and sexually transmitted diseases. It has broad and potent antibacterial activity over common Grampositive and -negative aerobic pathogens and obligate anaerobes. Different from the cephem antibiotics, levofloxacin is unique in its marked selectivity against members of the family Enterobacteriaceae and its negligible effect on predominant anaerobes. Levofloxacin also exhibits satisfactory antimicrobial effects in surgical infections and it may be used for treatment of gastrointestinal infections such as traveler’s diarrhea associated with the pathogenic Enterobacteriaceae.
InChI:InChI=1/C18H20FN3O4/c1-10-9-26-17-14-11(16(23)12(18(24)25)8-22(10)14)7-13(19)15(17)21-5-3-20(2)4-6-21/h7-8,10H,3-6,9H2,1-2H3,(H,24,25)/t10-/m0/s1
Articles related to Levofloxacin hydrochloride:
Article |
Source |
Experimental and computational study on the enantioseparation of four chiral fluoroquinolones by capillary electrophoresis with sulfated-β-cyclodextrin as chiral selector |
Ma, Qianyun,Cong, Wei,Liu, Ye,Geng, Zikai,Lin, Ying,Wang, Zhaokun , p. 549 - 557 (2021) |
Equilibrium and structural characterization of ofloxacin-cyclodextrin complexation |
Toth, Gergo,Mohacsi, Reka,Racz, Akos,Rusu, Aura,Horvath, Peter,Szente, Lajos,Beni, Szabolcs,Noszal, Bela , p. 291 - 300 (2013) |
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