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Merck
CN

SML4150

Ciprofloxacin hydrochloride hydrate

≥98% (HPLC), powder

Synonym(s):

1-Cyclopropyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid hydrochloride hydrate, 1-Cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic acid monohydrochloride, monohydrate

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About This Item

Empirical Formula (Hill Notation):
C17H18FN3O3·HCl · xH2O
CAS Number:
Molecular Weight:
367.80 (anhydrous basis)
MDL number:
NACRES:
NA.21
Assay:
≥98% (HPLC)
Form:
powder
Quality level:
Storage condition:
desiccated
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Quality Level

assay

≥98% (HPLC)

form

powder

storage condition

desiccated

color

white to beige

solubility

DMSO: 2 mg/mL, clear

storage temp.

-10 to -25°C

SMILES string

O=C(C1=CN(C2CC2)C3=CC(N4CCNCC4)=C(C=C3C1=O)F)O.Cl.[xH2O]

Application

Ciprofloxacin hydrochloride hydrate is suitable for use in research to study antibiotic resistance mechanisms. It is also used to inhibit cell proliferation and to sensitize cells to TRAIL (TNF-related apoptosis-inducing ligand) -Induced apotosis.

Biochem/physiol Actions

Ciprofloxacinis a fluoroquinolone antibiotic with broad-spectrum activity, which killsbacteria by blocking DNA gyrase and type IV topoisomerase—critical enzymes forDNA replication and transcription—leading to cell death. It is effectiveagainst a broad array of both Gram-positive and Gram-negative bacteria, inaddition to Mycoplasmas. While the hydrochloride form of ciprofloxacin ishighly soluble in water, ciprofloxacin itself is only sparingly soluble inaqueous solutions.

Disclaimer

Hygroscopic Store with desiccant


Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

新产品

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George G Zhanel et al.
Treatments in respiratory medicine, 5(6), 437-465 (2006-12-13)
The new respiratory fluoroquinolones (gatifloxacin, gemifloxacin, levofloxacin, moxifloxacin, and on the horizon, garenoxacin) offer many improved qualities over older agents such as ciprofloxacin. These include retaining excellent activity against Gram-negative bacilli, with improved Gram-positive activity (including Streptococcus pneumoniae and Staphylococcus
G S Davies et al.
The Journal of antimicrobial chemotherapy, 16(6), 713-717 (1985-12-01)
Ciprofloxacin appears to have useful activity against Pseudomonas aeruginosa. We have studied its in-vitro activity against ten strains of Ps. aeruginosa with multiple antibiotic resistance. We have confirmed that ciprofloxacin is very active against Ps. aeruginosa with minimal inhibitory concentrations
Raizza Zorman Marques et al.
Environmental pollution (Barking, Essex : 1987), 357, 124376-124376 (2024-06-20)
We compared the ability of one emergent (Sagittaria montevidensis), two floating (Salvinia minima and Lemna gibba), and one heterophyllous species (Myriophyllum aquaticum) to simultaneously remove sulfamethoxazole, sulfadiazine, ciprofloxacin, enrofloxacin, norfloxacin, levofloxacin, oxytetracycline, tetracycline, doxycycline, azithromycin, amoxicillin, and meropenem from wastewater



Global Trade Item Number

SKUGTIN
SML4150-50MG04065272699426
SML4150-10MG04065272699419