The store will not work correctly when cookies are disabled.
Parece que JavaScript está deshabilitado en su navegador. Para obtener la mejor experiencia en nuestro sitio, asegúrese de activar Javascript en su navegador.
· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items (±)-trans-ACPD - ≥99%(HPLC) , CAS No.67684-64-4
Synonyms
(1R,3S)-ACPD | Trans-( inverted exclamation markA)-ACP | 1-Amino-cyclopentane-1,3-dicarboxylic acid(trans-ACPD) | t-ACPD | SCHEMBL4835874 | 1-Amino-1,3-cyclopentanedicarboxylic acid | AJ-190/40848563 | BDBM50060136 | 1-Amino-1,3-dicarboxycyclopentane | BC
🧪
Why this grade ≥99%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
🌡
Storage & shipping Room temperature Ships Normal 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinónimos
(1R,3S)-ACPD | Trans-( inverted exclamation markA)-ACP | 1-Amino-cyclopentane-1,3-dicarboxylic acid(trans-ACPD) | t-ACPD | SCHEMBL4835874 | 1-Amino-1,3-cyclopentanedicarboxylic acid | AJ-190/40848563 | BDBM50060136 | 1-Amino-1,3-dicarboxycyclopentane | BC
Especificaciones y pureza
≥99%(HPLC)
Mecanismos bioquímicos y fisiológicos
Equimolecular mixture of (1S,3R)- and (1R,3S)-ACPD. Selective agonist for metabotropic glutamate receptors; active at both group I and group II mGlu receptors (EC50values are 2, 15, 23 and ~800μM at mGluR2, mGluR1, mGluR5and mGluR4respectively).(1S,3R)-AC
Condiciones de almacenamiento de almacenamiento
Room temperature
Nombres e identificadores Sonrisas canónicas C1CC(CC1C(=O)O)(C(=O)O)N IUPAC Name (1R,3S)-1-aminocyclopentane-1,3-dicarboxylic acid InChIKey YFYNOWXBIBKGHB-MHTLYPKNSA-N INCHI 1S/C7H11NO4/c8-7(6(11)12)2-1-4(3-7)5(9)10/h4H,1-3,8H2,(H,9,10)(H,11,12)/t4-,7+/m0/s1 Isómeros SMILES C1C[C@@](C[C@H]1C(=O)O)(C(=O)O)N Peso molecular 173.17 Reaxy-Rn 3031649 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3031649&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 Organic acids and derivatives Clase Carboxylic acids and derivatives Subclass Amino acids, peptides, and analogues Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives - Alpha amino acids Direct Parent L-alpha-amino acids Alternative Parents D-alpha-amino acids Dicarboxylic acids and derivatives Amino acids Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aliphatic homomonocyclic compounds Substituents D-alpha-amino acid - L-alpha-amino acid - Dicarboxylic acid or derivatives - Amino acid - Carboxylic acid - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Organic nitrogen compound - Carbonyl group - Amine - Organic oxide - Aliphatic homomonocyclic compound Descripción This compound belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom. 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.
Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad Solvent:water, Max Conc. mg/mL: None, Max Conc. mM: 5 with gentle warming; Solvent:1eq. NaOH, Max Conc. mg/mL: 8.66, Max Conc. mM: 50 Peso molecular 173.170 g/mol XLogP3 -3.200 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 2 Exact Mass 173.069 Da Monoisotopic Mass 173.069 Da Topological Polar Surface Area 101.000 Ų Heavy Atom Count 12 Formal Charge 0 Complexity 227.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 2 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 1
Calculadoras de soluciones Molarity Calculator Determine the necessary mass, volume, or concentration for preparing a solution.
Dilution Calculator Determine the dilution needed to prepare a stock solution.
Reconstitution Calculator Reseñas
We use cookies to ensure the website functions properly and, where permitted, to improve your experience. You can manage your preferences at any time in Settings. Learn more in our
Cookie Policy. Configuración Aceptar todo Rechazar
Shall we send you a message when we have discounts available?
Remind me later Permitir
Thank you! Please check your email inbox to confirm.
Oops! Notifications are disabled.
Products are supplied to verified businesses, institutions, and qualified professionals for research and development use only. Not for use in humans, animals, diagnosis, or therapy.
Copyright © 2023–present Aladdin Scientific Corp. All rights reserved.
