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· · COA & SDS available for every product · Same-day shipping on in-stock items Remacemide hydrochloride - ≥99%(HPLC) , CAS No.111686-79-4
Synonyms
REMACEMIDE HYDROCHLORIDE | 2-amino-N-(1,2-diphenylpropan-2-yl)acetamide hydrochloride | CCG-101055 | FT-0710086 | Remacemide (hydrochloride) | I1ST2B6HIM | Tox21_110956_1 | DTXSID9045683 | MLS000758316 | NCGC00025236-02 | 2-Amino-N-(1-methyl-1,2-diphenyle
Storage
Room temperature,Desiccated
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Why this grade ≥99%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature,Desiccated Ships Normal 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyms
REMACEMIDE HYDROCHLORIDE | 2-amino-N-(1, 2-diphenylpropan-2-yl)acetamide hydrochloride | CCG-101055 | FT-0710086 | Remacemide (hydrochloride) | I1ST2B6HIM | Tox21_110956_1 | DTXSID9045683 | MLS000758316 | NCGC00025236-02 | 2-Amino-N-(1-methyl-1, 2-diphenyle
Specifications & Purity
≥99%(HPLC)
Biochemical and Physiological Mechanisms
Non-competitive NMDA receptor antagonist; blocks ion channel and allosteric modulatory site (IC50= 8 - 68 mM). Anticonvulsantin vivoand metabolizes to a more potent desglycine analog. Weakly blocks voltage-dependent Na+channels (IC50= 161 mM).
Storage
Room temperature, Desiccated
Names and Identifiers Canonical Smiles CC(CC1=CC=CC=C1)(C2=CC=CC=C2)NC(=O)CN.Cl IUPAC Name 2-amino-N-(1,2-diphenylpropan-2-yl)acetamide;hydrochloride InChIKey HYQMIUSWZXGTCC-UHFFFAOYSA-N INCHI 1S/C17H20N2O.ClH/c1-17(19-16(20)13-18,15-10-6-3-7-11-15)12-14-8-4-2-5-9-14;/h2-11H,12-13,18H2,1H3,(H,19,20);1H Isomeric SMILES CC(CC1=CC=CC=C1)(C2=CC=CC=C2)NC(=O)CN.Cl WGK Germany 3 RTECS AB4349500 PubChem CID 60510 Molecular Weight 304.82
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 Phenylpropanoids and polyketides Class Stilbenes Subclass Not available Intermediate Tree Nodes Not available Direct Parent Stilbenes Alternative Parents Alpha amino acid amides Amphetamines and derivatives Phenylpropanes Secondary carboxylic acid amides Organopnictogen compounds Organic oxides Monoalkylamines Hydrochlorides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic homomonocyclic compounds Substituents Stilbene - Alpha-amino acid amide - Alpha-amino acid or derivatives - Amphetamine or derivatives - Phenylpropane - Monocyclic benzene moiety - Benzenoid - Amino acid or derivatives - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid derivative - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Primary amine - Hydrochloride - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Amine - Organic oxygen compound - Aromatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids. External Descriptors Not available 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 Solubility Solvent:water, Max Conc. mg/mL: 30.48, Max Conc. mM: 100 Molecular Weight 304.800 g/mol XLogP3 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 2 Rotatable Bond Count 5 Exact Mass 304.134 Da Monoisotopic Mass 304.134 Da Topological Polar Surface Area 55.100 Ų Heavy Atom Count 21 Formal Charge 0 Complexity 306.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 1 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 2
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