Amoxicillin - ≥98% , CAS No.26787-78-0

CAS: 26787-78-0 Cat. No.: A275272 Molecular Weight: 365.4 Beilstein Registry Number: 7507120 EC Number: 248-003-8
AVAILABLE TO ORDER
Synonyms
Amoxicillin (as trihydrate) | Damoxy | Metifarma capsules | Siganopen | UNII-9EM05410Q9 | BLP 1410 | BL-P 1410 | Amoxicillinum [INN-Latin] | Cemoxin | Ospamox | Moxal | Amoxidal | Hiconcil | Metafarma capsules | Amoxivet | DTXCID1017044 | Amoxicilina [INN
Storage
Store at -20°C,Desiccated
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
5g
A275272-5g
2
$94.90
25g
A275272-25g
5

$341.90

$427.90
Save $86.00 (20.10%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C,Desiccated Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

Quality documents

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

📚

Literature proof

Cited in 191 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Amoxicillin is an antibiotic with good oral absorption and broad spectrum antimicrobial activity

Specifications

Synonyms
Amoxicillin (as trihydrate) | Damoxy | Metifarma capsules | Siganopen | UNII-9EM05410Q9 | BLP 1410 | BL-P 1410 | Amoxicillinum [INN-Latin] | Cemoxin | Ospamox | Moxal | Amoxidal | Hiconcil | Metafarma capsules | Amoxivet | DTXCID1017044 | Amoxicilina [INN
Specifications & Purity
≥98%
Biochemical and Physiological Mechanisms
β-lactam antibiotic. 4-hydroxy analog of ampicillin. Shows antibacterial activity. Inhibits cross-linkage between linear peptidoglycan polymer chains of Gram-positive and Gram-negative bacterial cell walls.
Storage
Store at -20°C, Desiccated
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Note
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Properties
ALogP-2
Names and Identifiers
Pubchem Sid488183229
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488183229
Canonical SmilesCC1(C(N2C(S1)C(C2=O)NC(=O)C(C3=CC=C(C=C3)O)N)C(=O)O)C
IUPAC Name(2S,5R,6R)-6-[[(2R)-2-amino-2-(4-hydroxyphenyl)acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
InChIKeyLSQZJLSUYDQPKJ-NJBDSQKTSA-N
INCHI1S/C16H19N3O5S/c1-16(2)11(15(23)24)19-13(22)10(14(19)25-16)18-12(21)9(17)7-3-5-8(20)6-4-7/h3-6,9-11,14,20H,17H2,1-2H3,(H,18,21)(H,23,24)/t9-,10-,11+,14-/m1/s1
Isomeric SMILES CC1([C@@H](N2[C@H](S1)[C@@H](C2=O)NC(=O)[C@@H](C3=CC=C(C=C3)O)N)C(=O)O)C
WGK Germany 2
RTECS XH8300000
Molecular Weight 365.4
Beilstein 7507120
Reaxy-Rn 584293
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=584293&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
ClassLactams
SubclassBeta lactams
Intermediate Tree Nodes Penams
Direct ParentPenicillins
Alternative Parents N-acyl-alpha amino acids and derivatives  Alpha amino acid amides  Phenylacetamides  1-hydroxy-2-unsubstituted benzenoids  Aralkylamines  Thiazolidines  Tertiary carboxylic acid amides  Secondary carboxylic acid amides  Amino acids  Azetidines  Dialkylthioethers  Carboxylic acids  Thiohemiaminal derivatives  Azacyclic compounds  Monocarboxylic acids and derivatives  Hydrocarbon derivatives  Carbonyl compounds  Organopnictogen compounds  Monoalkylamines  Organic oxides  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Penicillin - N-acyl-alpha amino acid or derivatives - Alpha-amino acid amide - Alpha-amino acid or derivatives - Phenylacetamide - Phenol - 1-hydroxy-2-unsubstituted benzenoid - Aralkylamine - Benzenoid - Monocyclic benzene moiety - Thiazolidine - Tertiary carboxylic acid amide - Azetidine - Amino acid or derivatives - Secondary carboxylic acid amide - Carboxamide group - Amino acid - Azacycle - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Dialkylthioether - Hemithioaminal - Thioether - Primary aliphatic amine - Amine - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Organopnictogen compound - Organonitrogen compound - Organooxygen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Aromatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as penicillins. These are organic compounds containing the penicillin core structure, which is structurally characterized by a penam ring bearing two methyl groups at position 2, and an amide group at position 6 [starting from the sulfur atom at position 1].
External Descriptors penicillin
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
PDE5A Tclin Phosphodiesterase 5A (5113 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HMGCR Tclin HMG-CoA reductase (2475 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
INSR Tclin Insulin receptor (5558 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PGR Tclin Progesterone receptor (8562 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RARA Tclin Retinoic acid receptor alpha (1324 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACE Tclin Angiotensin-converting enzyme (1423 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD2 Tclin Dopamine D2 receptor (23596 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GABRA1 Tclin GABA receptor alpha-1 subunit (399 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAOA Tclin Monoamine oxidase A (11911 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD1 Tclin Dopamine D1 receptor (9720 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD4 Tchem Dopamine D4 receptor (7907 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A2 Tclin Norepinephrine transporter (10102 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HRH2 Tclin Histamine H2 receptor (5428 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA1D Tclin Alpha-1d adrenergic receptor (4171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAOB Tclin Monoamine oxidase B (8835 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR1B Tclin Serotonin 1b (5-HT1b) receptor (2801 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2A Tclin Serotonin 2a (5-HT2a) receptor (14758 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2C Tclin Serotonin 2c (5-HT2c) receptor (11471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AVPR2 Tclin Vasopressin V2 receptor (2912 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADORA1 Tclin Adenosine A1 receptor (17603 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AGTR1 Tclin Type-1 angiotensin II receptor (5176 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CALCR Tclin Calcitonin receptor (2215 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A4 Tclin Serotonin transporter (12625 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CRHR1 Tclin Corticotropin releasing factor receptor 1 (2996 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HRH1 Tclin Histamine H1 receptor (7573 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA1B Tclin Alpha-1b adrenergic receptor (2912 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRM1 Tclin Mu opioid receptor (19785 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD3 Tclin Dopamine D3 receptor (14368 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AVPR1A Tclin Vasopressin V1a receptor (5412 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRD1 Tclin Delta opioid receptor (15096 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRK1 Tclin Kappa opioid receptor (16155 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR3A Tclin Serotonin 3a (5-HT3a) receptor (3366 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GCGR Tclin Glucagon receptor (2563 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A3 Tclin Dopamine transporter (10535 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
bla Beta-lactamase TEM (457 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
mrcA Penicillin-binding protein 1A (31 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Htr7 Serotonin 7 (5-HT7) receptor (19 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Agtr2 Angiotensin II type 2 (AT-2) receptor (803 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ampC Beta-lactamase AmpC (62480 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
blaZ Beta-lactamase (285 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mc4r Melanocortin receptor 4 (1205 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ltc4s Leukotriene C4 synthase (1 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Sigmar1 Sigma opioid receptor (160 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Npy1r Neuropeptide Y receptor type 1 (8 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cckar Cholecystokinin A receptor (90 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ntsr1 Neurotensin receptor 1 (48 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pde4d Phosphodiesterase 4D (4 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Bdkrb1 Bradykinin B1 receptor (77 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nos2 Nitric oxide synthase, inducible (3573 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mapk1 MAP kinase ERK2 (650 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PDE6A Phosphodiesterase 6A (40 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mmp9 Matrix metalloproteinase 9 (38 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
metG Methionyl-tRNA synthetase (123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Enterococcus durans (113 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Salmonella paratyphi (588 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Streptococcus pneumoniae (31063 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Enterococcus (1748 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Eggerthella lenta (139 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Acinetobacter calcoaceticus subsp. anitratus (25 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Campylobacter jejuni (634 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Helicobacter pylori (3113 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pseudomonas fluorescens (1630 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pseudomonas putida (467 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Enterobacter cloacae (7976 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Proteus (150 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Proteus vulgaris (5823 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Providencia rettgeri (925 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Salmonella enterica subsp. enterica serovar Gallinarum (105 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Salmonella typhimurium (15756 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Shigella boydii (323 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Shigella flexneri (1836 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Yersinia enterocolitica (166 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Aeromonas (15 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Vibrio cholerae (1211 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Vibrio parahaemolyticus (473 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pasteurella multocida (1166 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Bacteroides fragilis (1445 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Bacteroides thetaiotaomicron (562 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Parabacteroides distasonis (282 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Porphyromonas gingivalis (651 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Fusobacterium mortiferum (179 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.

6 results found

Lot NumberCertificate TypeDateItem
F23281056Certificate of AnalysisOct 29, 2025 A275272
F23281057Certificate of AnalysisOct 13, 2025 A275272
C2429082Certificate of AnalysisJan 08, 2025 A275272
B2428024Certificate of AnalysisJul 04, 2023 A275272
F23281055Certificate of AnalysisJul 04, 2023 A275272
F2328278Certificate of AnalysisJul 04, 2023 A275272
Chemical and Physical Properties
SolubilitySoluble in water
Molecular Weight365.400 g/mol
XLogP3-2.000
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count7
Rotatable Bond Count4
Exact Mass365.105 Da
Monoisotopic Mass365.105 Da
Topological Polar Surface Area158.000 Ų
Heavy Atom Count25
Formal Charge0
Complexity590.000
Isotope Atom Count0
Defined Atom Stereocenter Count4
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
References
1. Siqi Zou, Li Yang, Ruoting Tang, Wumiti Aihemaiti, Ziang Cheng, Jiaxiong Li, Wei Tao, Yue Huang, Jiehua Ma, Chao Li.  (2025)  Monitoring probiotic viability in vivo using DNA nanodevice-decorated bacteria.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.165902]
2. Jilong Wang, Qi Xiang, Ye Han, Zeyu Ma, Wei Cheng, Jie Sun, Shaobin Wang.  (2025)  Metal-free heterogeneous electro-Fenton with solid polymer electrolytes: A novel self-supporting system for PPCPs decontamination.  Journal of Environmental Chemical Engineering,      [PMID:] [10.1016/j.jece.2025.117854]
3. Yong Yang, Xiaoling Lei, Dongliang Zhang, Fang Dong, Sheng Liu.  (2025)  A miniaturized battery-free wireless epidermal platform for multiplexed sweat biomarker monitoring.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.167787]
4. Yukun Zhang, Wenrui Zhang, Zongda Li, Mingping Shen, Haoqiang Liu, Fanxing Meng, Minwei Zhang.  (2025)  Flexible non-enzymatic electrochemical sensors with graphene nanoconfined ZrO2 composites for monitoring and discriminating multiple nitroaromatic organophosphorus pesticides.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2025.115049]
5. Jiahong Zheng, Xiudan Shi, Pengzhan Li, Zhiguo Zhao, Guangqiang Ding.  (2025)  Preparation of a Cs4PbBr6 NCs@PCDs ratiometric fluorescent probe and detection of amoxicillin.  NEW JOURNAL OF CHEMISTRY,      [PMID:] [10.1039/D5NJ02499D]
6. Yongyang Chen, Xiaomin Sun, Lijiao Zheng, Yuan Liu, Yimo Zhao, Shimeng Huang, Shanping Li.  (2023)  Synergistic catalysis degradation of amoxicillin by DBD plasma-catalyst system constructed by DBD plasma and Ce0.5Bi0.5VO4/HCP coating.  PROCESS SAFETY AND ENVIRONMENTAL PROTECTION,      [PMID:] [10.1016/j.psep.2023.11.044]
7. Huan Zhan, Xiaoyan Liu, Jinbing Huang, Xian Liu, Xulong Zhang, Jiaxiong Yao, Shiwei Xie.  (2023)  Iron electrocoagulation activated peracetic acid for efficient degradation of sulfamethoxazole.  CHEMICAL ENGINEERING RESEARCH & DESIGN,      [PMID:] [10.1016/j.cherd.2023.10.042]
8. Guangli Li, Xiaoman Qi, Jingtao Wu, Xuan Wan, Tianyu Wang, Ying Liu, Yuwei Chen, Yonghui Xia.  (2023)  Highly stable electrochemical sensing platform for the selective determination of pefloxacin in food samples based on a molecularly imprinted-polymer-coated gold nanoparticle/black phosphorus nanocomposite.  FOOD CHEMISTRY,      [PMID:37862994] [10.1016/j.foodchem.2023.137753]
9. Zhipeng Zhang, Yao Tian, Pengcheng Huang, Fang-Ying Wu.  (2019)  Using target-specific aptamers to enhance the peroxidase-like activity of gold nanoclusters for colorimetric detection of tetracycline antibiotics.  TALANTA,      [PMID:31816712] [10.1016/j.talanta.2019.120342]
10. Jingzhi Yang, Yami Ran, Shaopeng Liu, Chenhao Ren, Yuntian Lou, Pengfei Ju, Guoliang Li, Xiaogang Li, Dawei Zhang.  (2023)  Synergistic D-Amino Acids Based Antimicrobial Cocktails Formulated via High-Throughput Screening and Machine Learning.  Advanced Science,  11  (9): (2307173).  [PMID:38126652] [10.1002/advs.202307173]
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12. Jing Zhang, Miaoqi Liu, Bo Pang, Chun Liu, Junjun Ma, Jianrui Niu, Ruina Zhang.  (2023)  Ciprofloxacin degradation in microbubble ozonation combined with electro-generated H2O2 process: Operational parameters and oxidation mechanism.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2023.124676]
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163. Dan Chang, Hu Shi, Jianyang Feng, Yang Liu, Yanan Yan, Lihong Shi, Yongxing Yang, Shaomin Shuang, Chuan Dong.  (2025)  Coupling machine learning with smartphone-assisted sensing platform: sample-to-answer visual detection of amoxicillin using ratiometric fluorescence carbon dots.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2025.114505]
164. Li Wang, Fan Li, ShiMei Yin, DongYao Yue, Chen Li, Yatao Liu, Zhenbei Wang, Fei Qi.  (2025)  Enhancing photogenerated carrier utilization in facet-engineered bismuth oxyhalide with addition of peroxymonosulfate for accelerated amoxicillin removal from water.  APPLIED CATALYSIS B-ENVIRONMENTAL,      [PMID:] [10.1016/j.apcatb.2025.126131]
165. Liu Song, Sun Pengcheng, Wang Mingyue, Jiang Yujie, Li Jiaqi, Jia Yuyu, Sun Zhenhuan, Yang Yuting, Liu Hai, Lu Haojian, Wang Zuankai.  (2025)  Acousto-dewetting enables droplet microfluidics on superhydrophilic surfaces.  Nature Physics,      [PMID:] [10.1038/s41567-025-02844-6]
166. Jiang Minwen, Zheng Jie, Tang Yi, Liu Hai, Yao Yawen, Zhou Jianfei, Lin Wei, Ma Yuan, Liu Jin, Zhou Jiajing.  (2025)  Retrievable hydrogel networks with confined microalgae for efficient antibiotic degradation and enhanced stress tolerance.  Nature Communications,  16  (1): (1-10).  [PMID:40175365] [10.1038/s41467-025-58415-z]
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168. Boyu Liu, Yumeng Han, Zhenqing Zhang, Jianing Hao, Hao Wan, Yongguo Jin, Qi Xu.  (2025)  Preparation and Characterization of Dual-Network Multifunctional Hydrogels Based on Peach Gum Polysaccharides: Ultrafast Self-Healing Ability, Favorable Mechanical Tunability, and Controlled Release Properties.  Gels,  11  (4): (274).  [PMID:40277710] [10.3390/gels11040274]
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170. Zhen Li, Wenxuan Du, Xiren Xia, Xiang Yan, Yin Xu.  (2025)  Sustainable electro-activated periodate system for efficiently eliminating organic pollutants in water.  ELECTROCHIMICA ACTA,      [PMID:] [10.1016/j.electacta.2025.146202]
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172. Mengxiao Liu, Hanbin Wu, Yiqiao Xie, Li Zeng, Yiyang Xu, Chen Da, Yang Yu.  (2025)  Unraveling the role of oxygen in aeration-driven piezoelectric PMS activation process using oxygen vacancy engineered BTO.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2025.133950]
173. Fang Yang, Yongwei Han, Zhong Sun, Xixin Duan.  (2025)  Layered Double Hydroxide Composite Materials Based on Biochar from Low-Temperature Carbonization for Efficient and Simultaneous Degradation of Multiple Antibiotics in Water: Performance and Mechanism.  Journal of Environmental Chemical Engineering,      [PMID:] [10.1016/j.jece.2025.117560]
174. Jiafeng Wu, Lina Ji, Mingqin Kang, Siyi Liu, Jing Liu, Zhongping Dong, Shuyan Xiao.  (2025)  Cerium modification enhances oxidase-like activity of graphitic carbon nitride for tetracycline detection.  Materials Today Communications,      [PMID:] [10.1016/j.mtcomm.2025.113155]
175. Anqing Fu, Qiqi Chen, YuanJun Peng, Lili Liu, Guoliang Teng, Xufang Qian, Zhiping Wang.  (2025)  Nitrous oxide emissions induced by antibiotics during denitrification: the mediating role of carbon source on energy metabolism and electron transport chain.  Journal of Cleaner Production,      [PMID:] [10.1016/j.jclepro.2025.145996]
176. Youheng Pan, Tianyi Zhang, Yanyun Jin, Shixin Li, Jiandong Hu, Lanlan Li.  (2025)  Rapid and selective detection of furazolidone, chloramphenicol and dimetridazole using a multi-dimensional heterojunction electrochemical sensor.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2025.115807]
177. Yu Li, Anqi Sun, Yufan Yang, Zhouping Wang, Junsong Yang.  (2025)  Highly stable and luminescent ZIF-8@MAPbBr3 enhanced “turn on” fluorescent aptasensor for azlocillin monitoring.  TALANTA,      [PMID:41175849] [10.1016/j.talanta.2025.129021]
178. Li Wang, Chenyu Wang, Fan Li, Dongyao Yue, Chen Li, Yatao Liu, Zhenbei Wang, Fei Qi, Amir Ikhlaq, Jolanta Kumirska, Ewa Maria Siedlecka, Oksana Ismailova, Zukhra Kadirova.  (2025)  Enhanced photo-Fenton degradation for amoxicillin in aqueous by halogen-facet synergistic regulation of BiOX: Insights into photogenerated electron migration and oxidant activation.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:41176862] [10.1016/j.jcis.2025.139294]
179. Jinyan Luo, Yulong Han, Zikang Hu, Guanghua Lei, Huanhuan Lu, Hengye Chen, Li Yang, Xinming Lv, Wanjun Long, Haiyan Fu.  (2025)  Iron Ion-Mediated Nitrogen-Doped Carbon Dot Fluorescence Sensing for Accurate Detection of Fluoroquinolone in Food.  Food Frontiers,      [PMID:] [10.1002/fft2.70142]
180. Quang Phan Quang Huy, Khoa Huynh Anh, Nguyen Hoang Cao, Trung Nguyen Tran Nhat, Minh Dang Thanh Cong, Nhung Tran Nguyen Cam, Khoa Tran Dang, Nghia Nguyen Ngoc, Ha Huynh Ky Phuong, Hieu Nguyen Huu.  (2025)  Molecularly imprinted polymer modified g-C3N4 integrated into paper-based devices for colorimetric detection of amoxicillin.  MICROCHIMICA ACTA,  192  (12): (820).  [PMID:41247386] [10.1007/s00604-025-07717-6]
181. Yao Yang, Xiao-Fen Jia, Guang-Hui Cui, Qiu-Yue Huang, Miao-Miao Lin, Zong-Ming Shi, Hui Ye, Xue-Zhi Zhang.  (2025)  Jinghuaweikang capsule alleviates Helicobacter pylori-infected gastric mucosal inflammation and drug resistance by regulating intestinal microbiota and MAPK pathway.  Frontiers in Cellular and Infection Microbiology,      [PMID:41394107] [10.3389/fcimb.2025.1628594]
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183. Jiaojiao Shang, Ruohong Yu, Fanying Zeng, Zhenyu Xiang, Mengyuan Dai, Guolin He, Jing Shi.  (2026)  pH-Triggered Antibiotic Release from Nanofiber-Hydrogel Hybrid Dressing for Infected Wound Healing.  Journal of Materials Chemistry B,      [PMID:41568600] [10.1039/D5TB01773D]
184. Chenyan Lu, Dajie Zou, Ning Zhang, Huye Li, Yanyan Jia, Huan Wang.  (2026)  A novel “ON–OFF–ON” fluorescent sensor based on N,Br-doped carbon dots for the rapid detection of tannic acid and erythromycin.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2026.117036]
185. Tianyi Zhu, Jian Zhang, Danyi He, Yiwen Yang, Hailong Wang, Jianbo Wang, Longhua Guo, Lei Li, Jianrong Chen, Yanbo Zeng.  (2026)  Pyrene-based fluorescent molecularly imprinted polymer for rapid and selective detection of oxytetracycline based on inner filter effect.  Analytical Methods,      [PMID:41665257] [10.1039/D5AY02167G]
186. Bo Shen, Yuxin Hui, Qi Wang, Fei Wang, Derek Hao, Huayue Zhu, Liguo Shen, Hao Du.  (2026)  Fe/Mo bimetallic sites-decorated carbonaceous material via 3 electron photocatalytic oxygen reduction reaction pathway for ultra-efficient degradation of water pollutants.  APPLIED CATALYSIS B-ENVIRONMENTAL,      [PMID:] [10.1016/j.apcatb.2026.126521]
187. Yi Jintao, Fu Nani, Zhong Wenhui, Liu Xia, Zhou Anqi, Li Xun.  (2026)  A CQDs-doped europium-DPA framework for fluorescence and colorimetric dual-mode sensing of amoxicillin and ciprofloxacin.  ANALYTICAL AND BIOANALYTICAL CHEMISTRY,      [PMID:41718751] [10.1007/s00216-026-06405-5]
188. Mengxiao Liu, Li Zeng, Hanbin Wu, Yiyang Xu, Yang Yu.  (2026)  Elimination of antibiotic resistance genes by three-dimensional electrochemical activation of peroxymonosulfate using Co3O4@BTO particles.  Journal of Environmental Chemical Engineering,  14  (3): (122268).  [PMID:] [10.1016/j.jece.2026.122268]
189. Jiawen Li, Zhenghe Wang, Linhui Qian, Jianqiao Zhao, Zhengjun Zhang, Weipeng Wang.  (2026)  Hierarchical hotspot engineering for ultrasensitive antibiotics sensing in human body fluids.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2026.175631]
190. Zhenghang Lai, Yanping Ding, Yu Yang, Lei Cheng, Jingwen Wang, Yong Liu.  (2026)  Enhancing the Fenton-like activity of molybdenite through Fe(III) ions impregnation.  ENVIRONMENTAL TECHNOLOGY,      [PMID:] [10.1080/09593330.2026.2638425]
191. Yi Ming Jun.  (2026)  Design of a β-cyclodextrin-modified FeOOH/Al(OH)3 hybrid with interfacial activation for synergistic tetracycline enrichment and stabilization.  Journal of Water Process Engineering,      [PMID:] [10.1016/j.jwpe.2026.110232]
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