Benzoyl-DL-phenylalanine - ≥97%(T) , CAS No.2901-76-0

CAS: 2901-76-0 Cat. No.: B153162 Molecular Weight: 269.3 EC Number: 636-715-5
AVAILABLE TO ORDER
GRADE & PURITY ≥97%(T)
Synonyms
N-Benzoylphenylalanine # | HMS2288N06 | Benzoyl-dl-phenylalanine | DTXSID301311364 | HMS1659K12 | CHEBI:90419 | F3095-4679 | Phenylalanine, N-benzoyl- | HY-W128407 | B0302 | EN300-00202 | NSC96354 | NSC-96354 | SMR000062385 | 2-Benzamido-3-phenylpropanoic
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1g
B153162-1g
2

$12.90

$19.90
Save $7.00 (35.18%)
5g
B153162-5g
2

$46.90

$70.90
Save $24.00 (33.85%)
10g
B153162-10g
1

$84.90

$127.90
Save $43.00 (33.62%)
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Why this grade

≥97%(T) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
N-Benzoylphenylalanine # | HMS2288N06 | Benzoyl-dl-phenylalanine | DTXSID301311364 | HMS1659K12 | CHEBI:90419 | F3095-4679 | Phenylalanine, N-benzoyl- | HY-W128407 | B0302 | EN300-00202 | NSC96354 | NSC-96354 | SMR000062385 | 2-Benzamido-3-phenylpropanoic
Specifications & Purity
≥97%(T)
Storage
Room temperature
Shipped In
Normal
Purity
≥97%(T)
Names and Identifiers
Pubchem Sid488189200
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488189200
Canonical SmilesC1=CC=C(C=C1)CC(C(=O)O)NC(=O)C2=CC=CC=C2
IUPAC Name2-benzamido-3-phenylpropanoic acid
InChIKeyNPKISZUVEBESJI-UHFFFAOYSA-N
INCHI1S/C16H15NO3/c18-15(13-9-5-2-6-10-13)17-14(16(19)20)11-12-7-3-1-4-8-12/h1-10,14H,11H2,(H,17,18)(H,19,20)
Isomeric SMILES C1=CC=C(C=C1)CC(C(=O)O)NC(=O)C2=CC=CC=C2
Molecular Weight 269.3
Reaxy-Rn 2283892
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2283892&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

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✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives
Direct ParentPhenylalanine and derivatives
Alternative Parents N-acyl-alpha amino acids  Hippuric acids  Phenylpropanoic acids  Amphetamines and derivatives  Benzoyl derivatives  Secondary carboxylic acid amides  Monocarboxylic acids and derivatives  Carboxylic acids  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Phenylalanine or derivatives - Hippuric acid or derivatives - Hippuric acid - N-acyl-alpha-amino acid - N-acyl-alpha amino acid or derivatives - 3-phenylpropanoic-acid - Amphetamine or derivatives - Benzamide - Benzoic acid or derivatives - Benzoyl - Monocyclic benzene moiety - Benzenoid - Secondary carboxylic acid amide - Carboxamide group - Monocarboxylic acid or derivatives - Carboxylic acid - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organopnictogen compound - Organic nitrogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Aromatic homomonocyclic compound
DescriptionThis 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 Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(non-human)
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 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.

3 results found

Lot NumberCertificate TypeDateItem
I2117241Certificate of AnalysisJul 10, 2025 B153162
I2117360Certificate of AnalysisJul 10, 2025 B153162
I2117361Certificate of AnalysisJul 10, 2025 B153162
Chemical and Physical Properties
Melt Point(°C)187 °C
Molecular Weight269.290 g/mol
XLogP32.800
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count5
Exact Mass269.105 Da
Monoisotopic Mass269.105 Da
Topological Polar Surface Area66.400 Ų
Heavy Atom Count20
Formal Charge0
Complexity331.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
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. Chenyang Wang, Tiantian Guo, Rong Li, Shujuan Ma, Yinmao Wei, Junjie Ou.  (2025)  One-pot construction of monodisperse core-shell silica microsphere with quinine-containing hybrid fibrous shell for racemates separation.  ANALYTICA CHIMICA ACTA,      [PMID:40701719] [10.1016/j.aca.2025.344350]
Solution Calculators
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