Moxifloxacin HCl - ≥99% , Bacterial DNA gyrase inhibitor, CAS No.186826-86-8, Bacterial DNA gyrase inhibitor

CAS: 186826-86-8 Cat. No.: M129861 Molecular Weight: 437.89 Beilstein Registry Number: 8377447 EC Number: 641-756-7
AVAILABLE TO ORDER
GRADE & PURITY ≥99%
Synonyms
1-Cyclopropyl-6-fluoro-7-((4aS,7aS)-hexahydro-1H-pyrrolo[3,4-b]pyridin-6(2H)-yl)-8-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylicacidhydrochloride | MOXIFLOXACIN HCL [VANDF] | Q368941 | 3-Quinolinecarboxylic acid, 1-cyclopropyl-6-fluoro-1,4-dihydro-8-met
Storage
Store at 2-8°C
Shipped In
Wet ice
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Size
Status
Price
Qty
50mg
M129861-50mg
3
$9.90
100mg
M129861-100mg
3
$10.90
500mg
M129861-500mg
2

$11.90

$17.90
Save $6.00 (33.52%)
1g
M129861-1g
5

$20.90

$31.90
Save $11.00 (34.48%)
5g
M129861-5g
3

$57.90

$86.90
Save $29.00 (33.37%)
25g
M129861-25g
3

$146.90

$220.90
Save $74.00 (33.50%)
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Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Moxifloxacin is a fourth-generation synthetic fluoroquinolone antibacterial agent.
An antibacterial agent that inhibits the activities of Topo II (DNA gyrase) and topoisomerase IV.

Specifications

Synonyms
1-Cyclopropyl-6-fluoro-7-((4aS, 7aS)-hexahydro-1H-pyrrolo[3, 4-b]pyridin-6(2H)-yl)-8-methoxy-4-oxo-1, 4-dihydroquinoline-3-carboxylicacidhydrochloride | MOXIFLOXACIN HCL [VANDF] | Q368941 | 3-Quinolinecarboxylic acid, 1-cyclopropyl-6-fluoro-1, 4-dihydro-8-met
Specifications & Purity
≥99%
Biochemical and Physiological Mechanisms
Moxifloxacin Hydrochloride is the hydrochloride salt preparation of Moxifloxacin, an 8-methoxy-fluoroquinone compound with broad-spectrum bactericidal activity against gram-positive and gram-negative strains. 8-methoxy-fluoroquinones are described to inhi
Storage
Store at 2-8°C
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Action Type
INHIBITOR
Mechanism of action
Bacterial DNA gyrase inhibitor
Purity
≥99%
Names and Identifiers
Pubchem Sid504756488
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504756488
Canonical SmilesCOC1=C2C(=CC(=C1N3CC4CCCNC4C3)F)C(=O)C(=CN2C5CC5)C(=O)O.Cl
IUPAC Name7-[(4aS,7aS)-1,2,3,4,4a,5,7,7a-octahydropyrrolo[3,4-b]pyridin-6-yl]-1-cyclopropyl-6-fluoro-8-methoxy-4-oxoquinoline-3-carboxylic acid;hydrochloride
InChIKeyIDIIJJHBXUESQI-DFIJPDEKSA-N
INCHI1S/C21H24FN3O4.ClH/c1-29-20-17-13(19(26)14(21(27)28)9-25(17)12-4-5-12)7-15(22)18(20)24-8-11-3-2-6-23-16(11)10-24;/h7,9,11-12,16,23H,2-6,8,10H2,1H3,(H,27,28);1H/t11-,16+;/m0./s1
Isomeric SMILES COC1=C2C(=CC(=C1N3C[C@@H]4CCCN[C@@H]4C3)F)C(=O)C(=CN2C5CC5)C(=O)O.Cl
RTECS VB1983750
Alternate CAS 151096-09-2
Molecular Weight 437.89
Beilstein 8377447
Reaxy-Rn 11191843
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=11191843&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassQuinolines and derivatives
SubclassQuinoline carboxylic acids
Intermediate Tree Nodes Not available
Direct ParentQuinoline carboxylic acids
Alternative Parents Fluoroquinolones  Haloquinolines  Hydroquinolones  Aminoquinolines and derivatives  Hydroquinolines  Pyrrolopyridines  Pyridinecarboxylic acids  Methoxyanilines  Dialkylarylamines  Anisoles  Alkyl aryl ethers  Piperidines  Aryl fluorides  Pyrrolidines  Vinylogous amides  Heteroaromatic compounds  Amino acids  Monocarboxylic acids and derivatives  Azacyclic compounds  Dialkylamines  Carboxylic acids  Hydrocarbon derivatives  Hydrochlorides  Organic oxides  Organofluorides  Organopnictogen compounds  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Quinoline-3-carboxylic acid - Fluoroquinolone - Dihydroquinolone - Aminoquinoline - Haloquinoline - Dihydroquinoline - Pyridine carboxylic acid - Pyridine carboxylic acid or derivatives - Pyrrolopyridine - Methoxyaniline - Anisole - Dialkylarylamine - Tertiary aliphatic/aromatic amine - Alkyl aryl ether - Piperidine - Aryl fluoride - Pyridine - Aryl halide - Benzenoid - Pyrrolidine - Heteroaromatic compound - Vinylogous amide - Amino acid or derivatives - Amino acid - Tertiary amine - Azacycle - Carboxylic acid derivative - Carboxylic acid - Secondary aliphatic amine - Ether - Secondary amine - Monocarboxylic acid or derivatives - Organic oxide - Organopnictogen compound - Organic oxygen compound - Amine - Organic nitrogen compound - Hydrochloride - Organooxygen compound - Hydrocarbon derivative - Organohalogen compound - Organofluoride - Organonitrogen compound - Aromatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as quinoline carboxylic acids. These are quinolines in which the quinoline ring system is substituted by a carboxyl group at one or more positions.
External Descriptors hydrochloride
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
SMPD1 Tchem Sphingomyelin phosphodiesterase (13561 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Homo sapiens (32628 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HEK293 (82097 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FEN1 Tchem Flap endonuclease 1 (12055 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ABCC2 Tchem Canalicular multispecific organic anion transporter 1 (1191 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ABCB11 Tchem Bile salt export pump (2311 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ABCC3 Tbio Canalicular multispecific organic anion transporter 2 (718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ABCC4 Tchem Multidrug resistance-associated protein 4 (785 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Galc Galactocerebrosidase (11 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Streptococcus (3973 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Acinetobacter baumannii (41033 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cryptococcus neoformans (21258 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Streptococcus sp. 'group A' (3417 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ska Streptokinase A (5805 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

19 results found

Lot NumberCertificate TypeDateItem
C2113102Certificate of AnalysisJun 09, 2026 M129861
D2602096Certificate of AnalysisApr 10, 2026 M129861
D1503032Certificate of AnalysisMar 20, 2026 M129861
E2217163Certificate of AnalysisDec 12, 2025 M129861
E2217151Certificate of AnalysisDec 12, 2025 M129861
E2217145Certificate of AnalysisDec 12, 2025 M129861
A2416073Certificate of AnalysisOct 13, 2025 M129861
G2507026Certificate of AnalysisJul 21, 2025 M129861
D2508554Certificate of AnalysisAug 17, 2024 M129861
D2508538Certificate of AnalysisJun 13, 2024 M129861
D2523350Certificate of AnalysisJun 13, 2024 M129861
D2523353Certificate of AnalysisJun 13, 2024 M129861
B2514012Certificate of AnalysisMar 19, 2024 M129861
C2113101Certificate of AnalysisAug 16, 2023 M129861
H1920120Certificate of AnalysisMar 07, 2023 M129861
C2115012Certificate of AnalysisDec 15, 2022 M129861
C2115011Certificate of AnalysisDec 15, 2022 M129861
K2025230Certificate of AnalysisSep 19, 2022 M129861
C2115013Certificate of AnalysisFeb 16, 2022 M129861

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Chemical and Physical Properties
SolubilitySoluble in water (24 mg/ml), DMSO (88 mg/ml at 25 °C), and ethanol (<1 mg/ml at 25 °C).
Melt Point(°C)323.9-325°C
Molecular Weight437.900 g/mol
XLogP3
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count8
Rotatable Bond Count4
Exact Mass437.152 Da
Monoisotopic Mass437.152 Da
Topological Polar Surface Area82.100 Ų
Heavy Atom Count30
Formal Charge0
Complexity727.000
Isotope Atom Count0
Defined Atom Stereocenter Count2
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
Citations of This Product
References
1. Ayesha Younas, Zhuolin Dong, Ziye Hou, Muhammad Asad, Mengru Li, Nan Zhang.  (2023)  A chitosan/fucoidan nanoparticle-loaded pullulan microneedle patch for differential drug release to promote wound healing.  CARBOHYDRATE POLYMERS,      [PMID:36746584] [10.1016/j.carbpol.2023.120593]
2. Fan Mo, Yi Liu, Yingyin Xu, Qingsen He, Pengfei Sun, Xiaoping Dong.  (2022)  Photocatalytic elimination of moxifloxacin by two-dimensional graphitic carbon nitride nanosheets: Enhanced activity, degradation mechanism and potential practical application.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2022.121067]
Solution Calculators
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