- Fast and green method to synthesis of quinolone carboxylic acid derivatives using giant-ball nanoporous isopolyoxomolybdate as highly efficient recyclable catalyst in refluxing waterMirzaie, Yahya; Lari, Jalil; Vahedi, Hooshang; Hakimi, Mohammad; Nakhaei, Ahmad; et al, Journal of the Mexican Chemical Society, 2017, 61(1), 35-40
Cas no 93106-60-6 (Enrofloxacin)
Enrofloxacin is a broad-spectrum synthetic antimicrobial agent effective against a wide range of Gram-positive and Gram-negative bacteria. It exhibits bactericidal activity by inhibiting DNA gyrase, thereby preventing bacterial replication. Its stability in aqueous solutions and oral bioavailability make it suitable for use in veterinary medicine to treat various infections.
Enrofloxacin structure
Product Name:Enrofloxacin
CAS No:93106-60-6
MF:C19H22FN3O3
MW:359.394688129425
MDL:MFCD00792463
CID:61606
PubChem ID:24850748
Update Time:2025-07-21
Enrofloxacin Chemical and Physical Properties
Names and Identifiers
-
- Enrofloxacin
- 1-Cyclopropyl-7-(4-ethyl-1-piperazinyl)-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid
- Enrofloxacin Hcl
- 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(4-ethyl-1-piperazinyl)-3-quinolinecarboxylic acid
- 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(4-ethyl-1-piperazinyl)-quinoline-3-carboxylic acid
- 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(4-ethylpiperazino)-quinoline-3-carboxylic acid
- 1-cyclopropyl-7-(4-ethyl-1-piperazinyl)-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic
- Baytri
- bayvp2674
- BAY-Vp2674
- Enrofoxacin
- Enrolfoxacin
- PD160788
- ROFLOXACIN BASE
- WAKO059-07471
- 1-Cyclopropyl-7-(4-ethyl-1-piperazinyl)-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic Acid
- Baytril
- Enrofloxacine
- CFPQ
- Enrofloxacino
- Enrofloxacinum
- endrofloxicin
- BAY VP 2674
- Enrofloxacine [French]
- Enrofloxacinum [Latin]
- Enroxil
- Enrofloxacino [Spanish]
- 1-cyclopropyl-7-(4-ethylpiperazin-1-yl)-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid
- N-Ethylciprofloxacin
- Baytril (TN)
- ERFX
- Enrofloxacin [USAN:BAN:INN]
- 3DX3XEK1BN
- Enrofloxacin (USAN/INN)
- 3-Quinolinecarboxylic acid, 1-cyclopropyl-7-(4-ethyl-1-piperazinyl)-6-
- 1-Cyclopropyl-7-(4-ethyl-1-piperazinyl)-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid (ACI)
- 1-Cyclopropyl-6-fluoro-7-(4-ethyl-1-piperazinyl)-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid
- 1-Cyclopropyl-7-(4-ethyl-piperazin-1-yl)-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid
- 1-Cyclopropyl-7-(4-ethylpiperazin-1-yl)-6-fluoro-4-oxoquinoline-3-carboxylic acid
- Alsir
- BAY-Vp 2674
- Bayrocin
- Biofloxavet
- Enflocyna Sol
- Enrocin
- Enrodac
- Enrofan
- Enroflon
- Enrogil
- Enrovet
- Fortius
- N-Ethyl ciprofloxacin
- N′-Ethylciprofloxacin
- PD 160788
- Enrofloxacin for system suitability
- SR-01000000045
- BAY Vp 2674;PD160788
- 1-Cyclopropyl-7-(4-ethyl-1-piperazinyl)-6-Fluoro-1,4-Dihydro-4-Oxo-3-Quinolonecarboxylic Acid
- Enrofloxacin base
- Enroflox
- ENROFLOXACIN FOR VETERINARY USE (EP IMPURITY)
- Enrofloxacin, European Pharmacopoeia (EP) Reference Standard
- AC-7614
- 1-Cyclopropyl-7-(4-ethylpiperazin-1-yl)-6-fluoro-4-oxo-1
- 1-Cyclopropyl-7-(4-ethyl-1-piperazinyl)-6-fluoro-1,4-dihydro-4-oxo-3-quinolineca rboxyl acid
- ENROFLOXACIN [MI]
- MLS001076496
- Enrofloxacin, VETRANAL(TM), analytical standard
- BRD-K76534306-001-21-9
- 1-Cyclopropyl-7-(4-ethyl-1-piperazinyl)-6-fluoro-1,4-dihydro-4-oxo-3- quinolonecarboxylic acid
- ENROFLOXACIN 100
- SY052755
- 1-Cyclopropyl-7-(4-ethyl-1-piperazinyl)-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid, 9CI
- HY-B0502
- Enrofloxacin [USAN:USP:INN:BAN]
- 1-cyclopropyl-7-(4-ethylpiperazinyl)-6-fluoro-4-oxohydroquinoline-3-carboxylic acid
- D02473
- Enrofloxacin for veterinary use
- Enrofloxacinum (Latin)
- Enroflox Chewable Tablets
- 1,4-Dihydro-1-cyclopropyl-7-(4-ethyl-1-piperazinyl)-6-fluoro-4-oxo-3-quinolineca rboxyl acid
- Enrofloxacin (USAN:USP:INN:BAN)
- EnrositeFlavored
- ENROFLOXACIN [USP IMPURITY]
- Enroflox 100
- NCGC00018143-04
- Enrofloxacin 1000 microg/mL in Acetonitrile
- ENROFLOXACIN FOR VETERINARY USE (EP MONOGRAPH)
- HMS2052O09
- ENROFLOXACIN (USP-RS)
- NSC-758616
- HMS2234M11
- DB11404
- Enroflox Injection for Dogs 2.27%
- CAS-93106-60-6
- EnroMed 100
- ENROFLOXACIN [USP MONOGRAPH]
- AKOS005530685
- Bay-Vp-2674
- ENROFLOXACIN (USP MONOGRAPH)
- NSC 758616
- Pharmakon1600-01503721
- Tox21_110831_1
- ENROFLOXACIN FOR VETERINARY USE [EP MONOGRAPH]
- ENROFLOXACIN FOR VETERINARY USE [EP IMPURITY]
- 1-cyclopropyl-7-(4-ethylpiperazin-1-yl)-6-fluoro-4-oxo-quinoline-3-carboxylic acid
- CHEBI:35720
- Enrofloxacin, United States Pharmacopeia (USP) Reference Standard
- MLS001424169
- SCHEMBL149150
- HMS2090E12
- BAY-Vp2674;PD160788
- BCP15457
- 3-Quinolinecarboxylic acid, 1-cyclopropyl-7-(4-ethyl-1-piperazinyl)-6-fluoro-1,4-dihydro-4-oxo-
- NS00010889
- BRD-K76534306-001-22-7
- DB-057368
- AB00384269_17
- Enroquin
- Quellaxcin
- SPECTRUM1503721
- AB00384269_18
- SR-01000000045-3
- EnrofloxacinFlavored
- EnroMed
- NCGC00018143-05
- ALBB-030792
- BBL009982
- 1-CYCLOPROPYL-7-(4-ETHYLPIPERAZINO)-6-FLUORO-4-OXO-1,4-DIHYDRO-3-QUINOLINECARBOXYLIC ACID
- DTXSID1045619
- Enrofloxacin Antibacterial Injectable Solution
- MLS000069441
- NCGC00018143-02
- HMS3394O09
- ENROFLOXACIN [INN]
- CHEMBL15511
- Baytril Soft Chewable Tablets
- 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(4-ethyl-1-piperazinyl)-3-quinoline-carboxylic acid
- 93106-60-6
- Tenotryl
- 1,4-Dihydro-1-cyclopropyl-7-(4-ethyl-1-piperazinyl)-6-fluoro-4-oxo-3-quinolinecarboxylic acid
- FluroxinFlavored
- Enrofloxacin (USP/INN)
- Zobuxa
- HMS2093I21
- HMS3715B18
- ENROFLOXACIN [GREEN BOOK]
- BRD-K76534306-001-11-0
- s3059
- Enrofloxacin Flavored Tablets
- Enrosite
- Enrofloxacin, Pharmaceutical Secondary Standard; Certified Reference Material
- Enrofloxacin, >=98.0% (HPLC)
- CCG-101102
- HMS3373P14
- SolutionKitsEnrofloxacin
- ENROFLOXACIN [USAN]
- Enrofloxacin for system suitability, European Pharmacopoeia (EP) Reference Standard
- Tox21_110831
- NCGC00021632-03
- CCRIS 8214
- CPD000059011
- SBI-0206725.P001
- STK711109
- ENROFLOXACIN (USP IMPURITY)
- AB00384269-16
- Q414413
- HSDB 6952
- ENROFLOXACIN [MART.]
- UNII-3DX3XEK1BN
- Baytril Antibacterial Tablets, Baytril Taste Tabs Antibacterial Tablets
- NSC758616
- 3-Quinolinecarboxylic acid, 1,4-dihydro-1-cyclopropyl-7-(4-ethyl-1-piperazinyl)-6-fluoro-4-oxo-
- F81544
- KS-5010
- ENROFLOXACIN [USP-RS]
- ENROFLOXACIN [HSDB]
- E0786
- Baytril 100 Injectable Solution
- NC00352
- NCGC00018143-03
- NCGC00018143-01
- Baytril Antibacterial Injectable Solution
- BRN 5307824
- Fluroxinfor Dogs 2.27%
- DL-384
- ENROFLOXACIN (MART.)
- DTXCID9025619
- SMR000059011
- MFCD00792463
- Enroquin Antibacterial
- Opera_ID_1106
-
- MDL: MFCD00792463
- Inchi: 1S/C19H22FN3O3/c1-2-21-5-7-22(8-6-21)17-10-16-13(9-15(17)20)18(24)14(19(25)26)11-23(16)12-3-4-12/h9-12H,2-8H2,1H3,(H,25,26)
- InChI Key: SPFYMRJSYKOXGV-UHFFFAOYSA-N
- SMILES: O=C(C1C(=O)C2C(=CC(N3CCN(CC)CC3)=C(C=2)F)N(C2CC2)C=1)O
- BRN: 5307824
Computed Properties
- Exact Mass: 359.16500
- Monoisotopic Mass: 359.165
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 7
- Heavy Atom Count: 26
- Rotatable Bond Count: 4
- Complexity: 613
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: -0.2
- Topological Polar Surface Area: 64.099
- Surface Charge: 0
- Tautomer Count: nothing
Experimental Properties
- Color/Form: Powder
- Density: 1.3850
- Melting Point: 222.0 to 228.0 deg-C
- Boiling Point: 560.5°Cat760mmHg
- Flash Point: 292.8°C
- Solubility: biological extracorporealIn Vitro:DMSOsolubility9.5 mg/mL(26.43 mM;Need ultrasonic and warming)
- Water Partition Coefficient: Soluble in chloroform. Slightly soluble in water. Also soluble in dilute KOH
- PSA: 65.78000
- LogP: 2.31850
- Merck: 3592
Enrofloxacin Security Information
- Prompt:warning
- Signal Word:Warning
- Hazard Statement: H303
- Warning Statement: P312
- Hazardous Material transportation number:NONH for all modes of transport
- WGK Germany:3
- Hazard Category Code: 36/37/38
- Safety Instruction: S26; S36/37
- RTECS:VB1993650
-
Hazardous Material Identification:
- Toxicity:LD50 in male, female mice (mg/kg): >5000, 4336 orally; ~200, ~200 i.v.; in male rats, male rabbits (mg/kg): >5000, 500-800 orally (Altreuther)
- Storage Condition:Powder -20°C 3 years ? 4°C 2 years In solvent -80°C 6 months ? -20°C 1 month
- Risk Phrases:R36/37/38
Enrofloxacin Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | E114258-500g |
Enrofloxacin |
93106-60-6 | 98% | 500g |
¥1958.90 | 2023-09-03 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | E114258-5g |
Enrofloxacin |
93106-60-6 | 98% | 5g |
¥67.90 | 2023-09-03 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | E114258-1g |
Enrofloxacin |
93106-60-6 | 98% | 1g |
¥32.90 | 2023-09-03 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | E114258-100g |
Enrofloxacin |
93106-60-6 | 98% | 100g |
¥596.90 | 2023-09-03 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | E114258-25g |
Enrofloxacin |
93106-60-6 | 98% | 25g |
¥191.90 | 2023-09-03 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | E114257-100mg |
Enrofloxacin |
93106-60-6 | 100mg |
¥221.90 | 2023-09-03 | ||
| TI XI AI ( SHANG HAI ) HUA CHENG GONG YE FA ZHAN Co., Ltd. | E0786-25G |
Enrofloxacin |
93106-60-6 | >98.0%(T)(HPLC) | 25g |
¥190.00 | 2024-04-15 | |
| S e l l e c k ZHONG GUO | S3059-50mg |
Enrofloxacin |
93106-60-6 | 99.99% | 50mg |
¥791.33 | 2023-09-15 | |
| HE FEI BO MEI SHENG WU KE JI YOU XIAN ZE REN GONG SI | BE3208-100g |
Enrofloxacin |
93106-60-6 | ≥98% | 100g |
¥330元 | 2023-09-15 | |
| HE FEI BO MEI SHENG WU KE JI YOU XIAN ZE REN GONG SI | BE3208-25g |
Enrofloxacin |
93106-60-6 | ≥98% | 25g |
¥95元 | 2023-09-15 |
Enrofloxacin Production Method
Production Method 1
Reaction Conditions
1.1 Catalysts: Molybdate(42-), triacontakis[μ-(acetato-κO:κO′)]doheptacontaaquaoctacontahecta-μ… Solvents: Water ; 30 min, reflux
Reference
Production Method 2
Reaction Conditions
1.1 Reagents: Triethylamine Solvents: Dimethylformamide ; rt → 80 °C; 2 h, 80 °C
1.2 Reagents: Water ; cooled
1.2 Reagents: Water ; cooled
Reference
- Synthesis of labeled enrofloxacin-D5Xu, Zhong-jie; Lu, Wei-jing; Lu, Hao, Jingxi Huagong, 2012, 29(11), 1050-1052
Production Method 3
Reaction Conditions
1.1 25 min, 150 °C
Reference
- Conventional and microwave-assisted synthesis of quinolone carboxylic acid derivativesMirzaie, Y.; Lari, J.; Vahedi, H.; Hakimi, M., Russian Journal of General Chemistry, 2016, 86(12), 2865-2869
Production Method 4
Reaction Conditions
1.1 Reagents: Sodium hydroxide Solvents: Toluene ; 4 h, reflux
1.2 Reagents: Hydrochloric acid Solvents: Water
1.3 Solvents: Water ; 1 h, reflux; 14 h, 115 °C
1.2 Reagents: Hydrochloric acid Solvents: Water
1.3 Solvents: Water ; 1 h, reflux; 14 h, 115 °C
Reference
- Convenient one pot synthesis of some fluoroquinolones in aqueous mediaAbaee, M. Saeed; Sharifi, Ruhollah; Borhani, Shahin; Heravi, Majid M.; Motahari, Hossein, Heterocyclic Communications, 2005, 11(5), 415-418
Production Method 5
Reaction Conditions
1.1 Reagents: Diisopropylethylamine Catalysts: Potassium iodide Solvents: Acetonitrile , Water ; 0 °C; 16 h, rt
Reference
- Pharmacological characterization of 7-(4-(piperazin-1-yl)) ciprofloxacin derivatives: antibacterial activity, cellular accumulation, susceptibility to efflux transporters, and intracellular activityMarquez, Beatrice; Pourcelle, Vincent; Vallet, Coralie M.; Mingeot-Leclercq, Marie-Paule; Tulkens, Paul M.; et al, Pharmaceutical Research, 2014, 31(5), 1290-1301
Production Method 6
Reaction Conditions
1.1 Reagents: Sodium hydroxide Solvents: Water
1.2 Reagents: Acetic acid
1.2 Reagents: Acetic acid
Reference
- An improved process for the preparation of quinolone derivatives, e.g. ciprofloxacin, World Intellectual Property Organization, , ,
Production Method 7
Reaction Conditions
Reference
- Preparation of specific conjugation bridge linkers and immunoconjugates and methods of using them, World Intellectual Property Organization, , ,
Production Method 8
Reaction Conditions
Reference
- Preparation of bridge linkers used for specific conjugation of a cytotoxic agent to a cell-binding molecule, World Intellectual Property Organization, , ,
Production Method 9
Reaction Conditions
1.1 Catalysts: Zirconium dioxide (sulfonic acid derivative absorbed on ferrite) Solvents: Water ; 19 min, reflux
Reference
- Nano-Fe3O4@ZrO2-SO3H as Highly Efficient Recyclable Catalyst for the Green Synthesis of FluoroquinolonesNakhaei, Ahmad; Ramezani, Shirin; Shams-Najafi, Sayyed Jalal; Farsinejad, Sadaf, Letters in Organic Chemistry, 2018, 15(9), 739-746
Production Method 10
Reaction Conditions
1.1 Catalysts: Aluminum bromide Solvents: Ethanol ; 4 h, rt → 75 °C
1.2 Reagents: Sodium hydroxide Solvents: Water ; 30 min, 70 °C
1.3 Reagents: Hydrochloric acid Solvents: Water ; neutralized
1.2 Reagents: Sodium hydroxide Solvents: Water ; 30 min, 70 °C
1.3 Reagents: Hydrochloric acid Solvents: Water ; neutralized
Reference
- Preparation of norfloxacin, ciprofloxacin and enrofloxacin, China, , ,
Production Method 11
Reaction Conditions
1.1 Catalysts: Aluminum chloride Solvents: Isoamyl alcohol ; 8 h, 140 °C
1.2 Reagents: Hydrochloric acid Solvents: Water
1.3 Reagents: Hydroxide ; pH 7.2 - 7.3
1.2 Reagents: Hydrochloric acid Solvents: Water
1.3 Reagents: Hydroxide ; pH 7.2 - 7.3
Reference
- Methods for preparation of norfloxacin, ciprofloxacin and enrofloxacin, China, , ,
Production Method 12
Reaction Conditions
1.1 Catalysts: Cerium trichloride heptahydrate Solvents: Water ; rt → 100 °C; 10 h, 99 °C
1.2 Reagents: Methanol ; 0.5 h, reflux; reflux → 5 °C; 1 h, 5 - 8 °C
1.2 Reagents: Methanol ; 0.5 h, reflux; reflux → 5 °C; 1 h, 5 - 8 °C
Reference
- Process for preparation of carbostyril medicines, China, , ,
Production Method 13
Reaction Conditions
1.1 Reagents: Potassium carbonate Solvents: Water ; 10 h, 90 - 95 °C; 90 °C → rt
1.2 Reagents: Hydrochloric acid Solvents: Water ; 3 h, pH 7.5, rt
1.2 Reagents: Hydrochloric acid Solvents: Water ; 3 h, pH 7.5, rt
Reference
- Process for the preparation of fluoroquinolone-3-carboxylic acids via amination of alkyl fluoro(haloquinolone)carboxylates with amines, France, , ,
Production Method 14
Reaction Conditions
1.1 Reagents: Potassium carbonate Solvents: Dimethylformamide ; 2 h, 120 °C
1.2 Reagents: Acetic acid , Hydrochloric acid Solvents: Water ; 4 h, 90 °C
1.3 Solvents: Isoamyl alcohol ; 6 h, 110 - 115 °C
1.2 Reagents: Acetic acid , Hydrochloric acid Solvents: Water ; 4 h, 90 °C
1.3 Solvents: Isoamyl alcohol ; 6 h, 110 - 115 °C
Reference
- Synthesis of derivatives of 1-ethyl-6-fluoro-7-(1-piperazinyl)-1,4-dihydro-4-oxo-quinoline-3-carboxylic acidXie, Jiangang; Liao, Xincheng; Qu, Lingbo; Tian, Mengchao, Zhengzhou Daxue Xuebao, 2003, 35(3), 75-78
Production Method 15
Reaction Conditions
Reference
- New process for the preparation of 1-cyclopropyl-3-quinolinecarboxylic acid derivatives, Spain, , ,
Production Method 16
Reaction Conditions
1.1 Solvents: Dimethyl sulfoxide
Reference
- Cycloaracylation of enamines. I. Synthesis of 4-quinolone-3-carboxylic acidsGrohe, Klaus; Heitzer, Helmut, Liebigs Annalen der Chemie, 1987, (1), 29-37
Production Method 17
Reaction Conditions
Reference
- Preparation of bridge linkers used for specific conjugation of two or more cytotoxic agents to a cell-binding molecule, World Intellectual Property Organization, , ,
Production Method 18
Reaction Conditions
Reference
- Preparation of novel bridge linkers containing an acetylenedicarbonyl group for specific conjugation of a cytotoxic agent to a cell-binding molecule, World Intellectual Property Organization, , ,
Production Method 19
Reaction Conditions
Reference
- Preparation of hydrophilic linkers for the conjugation of a cytotoxic agent or a chromophore to a cell-binding molecule, World Intellectual Property Organization, , ,
Enrofloxacin Raw materials
- 3-Quinolinecarboxylic acid, 1-cyclopropyl-7-(4-ethyl-1-piperazinyl)-6-fluoro-1,4-dihydro-4-oxo-, methyl ester
- Ethyl 1-Cyclopropyl-6,7-difluoro-4-oxo-1,4-dihydro-3-quinolinecarboxylate
- Methyl 3-(cyclopropylamino)-2-(2,4-dichloro-5-fluorobenzoyl)acrylate
- 1-Ethylpiperazine
- Ciprofloxacin
- 7-Chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-quinoline-3-carboxylic Acid
- Ciprofloxacin monohydrochloride
- Benzenepropanoic acid,2,4-dichloro-a-[(cyclopropylamino)methylene]-5-fluoro-b-oxo-, ethyl ester
Enrofloxacin Preparation Products
Enrofloxacin Suppliers
Amadis Chemical Company Limited
Gold Member
(CAS:93106-60-6)Enrofloxacin
Order Number:A844445
Stock Status:in Stock
Quantity:500g
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 07:03
Price ($):356.0
Email:[email protected]
Shanghai Jinhuan Chemical CO., LTD.
Gold Member
(CAS:93106-60-6)Enrofloxacin
Order Number:JH199
Stock Status:in Stock
Quantity:25kg
Purity:98.00%
Pricing Information Last Updated:Monday, 8 January 2024 17:37
Price ($): negotiated
Email:[email protected]
Tiancheng Chemical (Jiangsu) Co., Ltd
Gold Member
(CAS:93106-60-6)Enrofloxacin
Order Number:LE9804;LE26562144
Stock Status:in Stock
Quantity:25KG,200KG,1000KG
Purity:99%
Pricing Information Last Updated:Friday, 20 June 2025 12:02
Price ($):discuss personally
Email:[email protected]
Zhengzhou Baoyu Pharmaceutical Co., Ltd.
Gold Member
(CAS:93106-60-6)Enrofloxacin
Order Number:LE339
Stock Status:in Stock
Quantity:5KG/1KG/25KG/100KG
Purity:99% HPLC
Pricing Information Last Updated:Thursday, 14 August 2025 14:44
Price ($):negotiated
Email:[email protected]
Enrofloxacin Related Literature
-
Gloria Belén Ramírez-Rodríguez,José Manuel Delgado-López,Jaime Gómez-Morales CrystEngComm, 2013,15, 2206-2212
-
Hanie Hashtroudi,Ian D. R. Mackinnon J. Mater. Chem. C, 2020,8, 13108-13126
-
Guiying Zhang,Maosheng Cheng,Yanni Li,Keliang Liu,Lifeng Cai Chem. Commun., 2013,49, 11086-11088
-
Olga Guselnikova,Gérard Audran,Jean-Patrick Joly,Andrii Trelin,Evgeny V. Tretyakov,Vaclav Svorcik,Oleksiy Lyutakov,Sylvain R. A. Marque Chem. Sci., 2021,12, 4154-4161
-
Christopher B. Rodell,Christopher B. Highley,Minna H. Chen,Neville N. Dusaj,Chao Wang,Lin Han,Jason A. Burdick Soft Matter, 2016,12, 7839-7847
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