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· · COA & SDS available for every product · Same-day shipping on in-stock items N-Acetyl-DL-phenylalanine - ≥98%(HPLC) , CAS No.2901-75-9
Synonyms
DivK1c_000395 | SY040647 | Afalaninum [INN-Latin] | FT-0658752 | CHEBI:21626 | 2-acetamido-3-phenylpropanoic acid | 2-acetamido-3-phenyl-propanoic acid | DTXSID3045697 | SPBio_001563 | A819720 | DL-Phenylalanine, N-acetyl- | D88538 | EN300-933103 | FFW2NG
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Why this grade ≥98%(HPLC) 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyms
DivK1c_000395 | SY040647 | Afalaninum [INN-Latin] | FT-0658752 | CHEBI:21626 | 2-acetamido-3-phenylpropanoic acid | 2-acetamido-3-phenyl-propanoic acid | DTXSID3045697 | SPBio_001563 | A819720 | DL-Phenylalanine, N-acetyl- | D88538 | EN300-933103 | FFW2NG
Specifications & Purity
≥98%(HPLC)
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Pubchem Sid 504750520 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504750520 Canonical Smiles CC(=O)NC(CC1=CC=CC=C1)C(=O)O IUPAC Name 2-acetamido-3-phenylpropanoic acid InChIKey CBQJSKKFNMDLON-UHFFFAOYSA-N INCHI 1S/C11H13NO3/c1-8(13)12-10(11(14)15)7-9-5-3-2-4-6-9/h2-6,10H,7H2,1H3,(H,12,13)(H,14,15) Isomeric SMILES CC(=O)NC(CC1=CC=CC=C1)C(=O)O Molecular Weight 207.23 Reaxy-Rn 2213851 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2213851&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 Class Carboxylic acids and derivatives Subclass Amino acids, peptides, and analogues Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives Direct Parent Phenylalanine and derivatives Alternative Parents N-acyl-alpha amino acids Phenylpropanoic acids Amphetamines and derivatives Propargyl-type 1,3-dipolar organic compounds Monocarboxylic acids and derivatives Carboxylic acids Carboximidic acids Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic homomonocyclic compounds Substituents Phenylalanine or derivatives - N-acyl-alpha-amino acid - N-acyl-alpha amino acid or derivatives - 3-phenylpropanoic-acid - Amphetamine or derivatives - Monocyclic benzene moiety - Benzenoid - Carboximidic acid - Carboximidic acid derivative - Carboxylic acid - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Aromatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as phenylalanine and derivatives. These are compounds containing phenylalanine or a derivative thereof resulting from reaction of phenylalanine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. External Descriptors N-acetyl-amino acid - phenylalanine derivative 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 Melt Point(°C) 154 °C Molecular Weight 207.230 g/mol XLogP3 0.600 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 4 Exact Mass 207.09 Da Monoisotopic Mass 207.09 Da Topological Polar Surface Area 66.400 Ų Heavy Atom Count 15 Formal Charge 0 Complexity 234.000 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 1
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