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Levofloxacin hydrochloride

  • Product Name: Levofloxacin hydrochloride
  • CasNo: 100986-85-4
  • Purity:
  • Appearance: Slight yellow powder

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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.

What is the Levofloxacin hydrochloride ?

Levofloxacin hydrochloride is Slight yellow powder, while it's Molecular Formula is C18H20FN3O4. Antibacterial.

What is the CAS number for Levofloxacin hydrochloride ?

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)

What is Levofloxacin hydrochloride (100986-85-4) used for?

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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