Levofloxacin structure, CAS 100986-85-4

Levofloxacin

CAS Number100986-85-4

SynonymsLevofloxacin; L-Ofloxacin; S-(-)-Ofloxacin; MFCD03265511; Levaquin; levoflaxacin; Tavanic

Molecular FormulaC18H20FN3O4

Molecular Weight361.37

Purity98.0-102.0 anhydrous basis (HPLC)%

Density1.5±0.1 g/cm3

Boiling Point571.5±50.0 °C at 760 mmHg

Melting Point218ºC

Flash Point

Appearancepowder or crystals

EINECS

MSDSChineseEnglish

SymbolTransport

Signal WordWarning

Cat. No.: 2A-9011173 Purity: 98.0-102.0 anhydrous basis (HPLC)%
Change View

Please Login or Create an Account to: See VlP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

Quality Control of [ 100986-85-4 ] Purity: 98.0-102.0 anhydrous basis (HPLC)% SDS Specification MoL

Chemical & Physical Properties
CAS Number100986-85-4
Catalog No.2A-9011173
Chinese Name左氧氟沙星
SynonymsLevofloxacin; L-Ofloxacin; S-(-)-Ofloxacin; MFCD03265511; Levaquin; levoflaxacin; Tavanic
Molecular FormulaC18H20FN3O4
Molecular Weight361.37
Purity98.0-102.0 anhydrous basis (HPLC)
Density1.5±0.1 g/cm3
Boiling Point571.5±50.0 °C at 760 mmHg
Melting Point218ºC
Appearancepowder or crystals
Storage ConditionSealed and stored in a cool, dry warehouse.
ApplicationLevofloxacin is a synthetic fluoroquinolone antibiotic that inhibits the supercoiling activity of bacterial DNA gyrase and prevents DNA replication.
HTC2934999090
PubChem ID57648297
MDL NumberMFCD00865049
SMILESOC(C(C1=O)=CN2C(C1=CC(F)=C3N4CCN(C)CC4)=C3OC[C@@H]2C)=O
InChI1S/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
InChI KeyGSDSWSVVBLHKDQ-JTQLQIEISA-N
Beilstein/REAXYS7327015
NACRES CodeNA.85
UNSPSC51102829
Hazard SymbolsTransport
MSDSmsds/11173_1_100986_85_4.pdf
BioactivityLevofloxacin, a synthetic fluoroquinolone, is an antibacterial agent that inhibits the supercoiling activity of bacterial DNA gyrase, halting DNA replication.Target: AntibacterialLevofloxacin reduced bacterial load compared with placebo by 4.9-fold (95% confidence interval, 1.4-25.7; P=0.02) at day 7 but had no effect at any point on any marker of neutrophilic airway inflammation. In patients with a baseline bacterial load of more than 10(6) cfu/mL, levofloxacin treatment was associated with a 26.5% (95% confidence interval, 1.8%-51.3%; P=0.04) greater reduction in the percentage neutrophil count compared with placebo at day 7 [1]. Levofloxacin was found to significantly improve the clinical and microbiological parameters in CP individuals [2]. A 30-day course of levofloxacin does not significantly improve BK viral load reduction or allograft function when used in addition to overall reduction of immunosuppression [3]. Related Catalog Signaling Pathways >> Anti-infection >> Bacterial Research Areas >> Infection References [1]. Siva, R., et al., Effect of levofloxacin on neutrophilic airway inflammation in stable COPD: a randomized, double-blind, placebo-controlled trial. Int J Chron Obstruct Pulmon Dis, 2014. 9: p. 179-86. [2]. Pradeep, A.R., et al., Clinical and microbiological effects of levofloxacin in the treatment of chronic periodontitis: a randomized, placebo-controlled clinical trial. J Investig Clin Dent, 2014. [3]. Lee, B.T., et al., Efficacy of Levofloxacin in the Treatment of BK Viremia: A Multicenter, Double-Blinded, Randomized, Placebo-Controlled Trial. Clin J Am Soc Nephrol, 2014. Chemical & Physical Properties Density 1.5±0.1 g/cm3 Boiling Point 571.5±50.0 °C at 760 mmHg Melting Point 218ºC Molecular Formula C18H20FN3O4 Molecular Weight 361.367 Flash Point 299.4±30.1 °C Exact Mass 361.143799 PSA 75.01000 LogP 0.84 Vapour Pressure 0.0±1.7 mmHg at 25°C Index of Refraction 1.670 InChIKey GSDSWSVVBLHKDQ-JTQLQIEISA-N SMILES CC1COc2c(N3CCN(C)CC3)c(F)cc3c(=O)c(C(=O)O)cn1c23 Storage condition Store at 0-5°C
Use ofLevofloxacin, a synthetic fluoroquinolone, is an antibacterial agent that inhibits the supercoiling activity of bacterial DNA gyrase, halting DNA replication.Target: AntibacterialLevofloxacin reduced bacterial load compared with placebo by 4.9-fold (95% confidence interval, 1.4-25.7; P=0.02) at day 7 but had no effect at any point on any marker of neutrophilic airway inflammation. In patients with a baseline bacterial load of more than 10(6) cfu/mL, levofloxacin treatment was associated with a 26.5% (95% confidence interval, 1.8%-51.3%; P=0.04) greater reduction in the percentage neutrophil count compared with placebo at day 7 [1]. Levofloxacin was found to significantly improve the clinical and microbiological parameters in CP individuals [2]. A 30-day course of levofloxacin does not significantly improve BK viral load reduction or allograft function when used in addition to overall reduction of immunosuppression [3]. Properties Articles443 Name levofloxacin Synonym More Synonyms Levofloxacin Biological Activity Description Levofloxacin, a synthetic fluoroquinolone, is an antibacterial agent that inhibits the supercoiling activity of bacterial DNA gyrase, halting DNA replication.Target: AntibacterialLevofloxacin reduced bacterial load compared with placebo by 4.9-fold (95% confidence interval, 1.4-25.7; P=0.02) at day 7 but had no effect at any point on any marker of neutrophilic airway inflammation. In patients with a baseline bacterial load of more than 10(6) cfu/mL, levofloxacin treatment was associated with a 26.5% (95% confidence interval, 1.8%-51.3%; P=0.04) greater reduction in the percentage neutrophil count compared with placebo at day 7 [1]. Levofloxacin was found to significantly improve the clinical and microbiological parameters in CP individuals [2]. A 30-day course of levofloxacin does not significantly improve BK viral load reduction or allograft function when used in addition to overall reduction of immunosuppression [3]. Related Catalog Signaling Pathways >> Anti-infection >> Bacterial Research Areas >> Infection References [1]. Siva, R., et al., Effect of levofloxacin on neutrophilic airway inflammation in stable COPD: a randomized, double-blind, placebo-controlled trial. Int J Chron Obstruct Pulmon Dis, 2014. 9: p. 179-86. [2]. Pradeep, A.R., et al., Clinical and microbiological effects of levofloxacin in the treatment of chronic periodontitis: a randomized, placebo-controlled clinical trial. J Investig Clin Dent, 2014. [3]. Lee, B.T., et al., Efficacy of Levofloxacin in the Treatment of BK Viremia: A Multicenter, Double-Blinded, Randomized, Placebo-Controlled Trial. Clin J Am Soc Nephrol, 2014. Chemical & Physical Properties Molecular Formula C18H20FN3O4 Exact Mass 361.143799 PSA 75.01000 Index of Refraction 1.670 InChIKey GSDSWSVVBLHKDQ-JTQLQIEISA-N
Tax Rebate13.0%
SupervisionNone. MFN tariff: 6.5%. Ordinary tariff: 20.0%
Transport InfoShipping Name: UN
MSDS Transport InfoModule 14. Shipping information 14.1 UN dangerous goods number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 United Nations shipping name European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Danger Regulations: No International Maritime Danger Regulations International Air Transport Danger Regulations: No Marine pollutants (yes/no): No 14.6 Special reminder to users No data available
Related Products in API & Advanced Intermediates
Lamotrigine84057-84-12A-9011119
Lansoprazole103577-45-32A-9011124
Lansoprazole Sulphide compound103577-40-82A-9011125
Letrozole112809-51-52A-9011156
Levodopa59-92-72A-9011171
levofloxacin Mesylate226578-51-42A-9011174
Lincomycin hydrochloride7179-49-92A-9011191
Linezolid165800-03-32A-9011192
Lisinopril83915-83-72A-9011203
Lopinavir192725-17-02A-9011228
Browse all API & Advanced Intermediates products »
Contact Us

Phone:

630-322-8886

630-322-8887

Email:

[email protected]

Office Locations:

Chicago, IL, USA

San Francisco, CA, USA