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· · COA & SDS available for every product · Same-day shipping on in-stock items Ampicillin trihydrate - Moligand™,≥99%(HPLC)(dry basis) , CAS No.7177-48-2
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥99%(HPLC)(dry basis) Synonyms
CHEBI:31209 | Amcill (TN) | HMS2095G10 | AMPICILLIN TRIHYDRATE [WHO-IP] | Cymbi | MFCD00072036 | Ampicillin hydrate | AMPICILLIN TRIHYDRATE [WHO-DD] | Ampicillin hydrate (JP17) | AMPICILLIN TRIHYDRATE [EP MONOGRAPH] | D-(-)--Aminobenzylpenicillin (trihydr
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Why this grade Moligand™,≥99%(HPLC)(dry basis) Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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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 288 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Overview Chemical structure: ß-lactam
Application
Ampicillin Trihydrate is commonly used to select for ampicillin resistance in mutated and transformed cells.
Other Notes
Keep container tightly closed in a dry and well-ventilated place.
Specifications Synonyms
CHEBI:31209 | Amcill (TN) | HMS2095G10 | AMPICILLIN TRIHYDRATE [WHO-IP] | Cymbi | MFCD00072036 | Ampicillin hydrate | AMPICILLIN TRIHYDRATE [WHO-DD] | Ampicillin hydrate (JP17) | AMPICILLIN TRIHYDRATE [EP MONOGRAPH] | D-(-)--Aminobenzylpenicillin (trihydr
Specifications & Purity
Moligand™,≥99%(HPLC)(dry basis)
Biochemical and Physiological Mechanisms
A β-lactam antibiotic with an amino group side chain attached to the penicillin structure. Penicillin derivative that inhibits bacterial cell-wall synthesis (peptidoglycan cross-linking) by inactivating transpeptidases on the inner surface of the bacteria
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥99%(HPLC)(dry basis)
Names and Identifiers Canonical Smiles
CC1(C(N2C(S1)C(C2=O)NC(=O)C(C3=CC=CC=C3)N)C(=O)O)C.O.O.O
IUPAC Name
(2S,5R,6R)-6-[[(2R)-2-amino-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid;trihydrate
InChIKey
RXDALBZNGVATNY-CWLIKTDRSA-N
INCHI
1S/C16H19N3O4S.3H2O/c1-16(2)11(15(22)23)19-13(21)10(14(19)24-16)18-12(20)9(17)8-6-4-3-5-7-8;;;/h3-7,9-11,14H,17H2,1-2H3,(H,18,20)(H,22,23);3*1H2/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=CC=C3)N)C(=O)O)C.O.O.O
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=54277913&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 Kingdom Organic compounds Superclass Organoheterocyclic compounds Class Lactams Subclass Beta lactams Intermediate Tree Nodes Penams Direct Parent Penicillins Alternative Parents N-acyl-alpha amino acids and derivatives Alpha amino acid amides Phenylacetamides Aralkylamines Thiazolidines Tertiary carboxylic acid amides Secondary carboxylic acid amides Amino acids Azetidines Thiohemiaminal derivatives Monocarboxylic acids and derivatives Azacyclic compounds Dialkylthioethers Carboxylic acids Carbonyl compounds Hydrocarbon derivatives Monoalkylamines Organic oxides Organopnictogen compounds Molecular Framework Aromatic heteropolycyclic compounds Substituents Penicillin - N-acyl-alpha amino acid or derivatives - Alpha-amino acid amide - Alpha-amino acid or derivatives - Phenylacetamide - Aralkylamine - Monocyclic benzene moiety - Benzenoid - Thiazolidine - Tertiary carboxylic acid amide - Amino acid or derivatives - Azetidine - Amino acid - Carboxamide group - Secondary carboxylic acid amide - 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 - Primary amine - Hydrocarbon derivative - Aromatic heteropolycyclic compound Description This 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 hydrate Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Sensitivity heat sensitive Specific Rotation[α] 293° (C=0.5,H2O) Melt Point(°C) 198-200°C Molecular Weight 403.500 g/mol XLogP3 Hydrogen Bond Donor Count 6 Hydrogen Bond Acceptor Count 9 Rotatable Bond Count 4 Exact Mass 403.141 Da Monoisotopic Mass 403.141 Da Topological Polar Surface Area 141.000 Ų Heavy Atom Count 27 Formal Charge 0 Complexity 562.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 4 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 4
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Reconstitution Calculator Reviews Need help choosing the grade? Our grade selection guide covers purity, stabilizer status, and application suitability for all variants in our catalog.
View Moligand™ grade guide →
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