4-chloro-d-phenylalanine - ≥95% , CAS No.14091-08-8

CAS: 14091-08-8 Cat. No.: C131971 Peso molecular: 199.63 Número EC: 634-290-0
Disponible para pedir
GRADE & PURITY ≥95%
Synonyms
EN300-366578 | NCGC00024889-01 | P-CHLORO-D-PHENYLALANINE | RSS1JQ7MES | AM82750 | AKOS016842281 | FS-2457 | (R)-2-Amino-3-(4-chlorophenyl)propionic Acid Hydrochloride | Z995228428 | d-p-chlorophenylalanine | NCGC00015255-01 | AC-5845 | (R)-4-Chlorophenyl
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
250mg
C131971-250mg
3
9,90US$
1g
C131971-1g
1
14,90US$
5g
C131971-5g
2
39,90US$
25g
C131971-25g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
176,90US$
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C Ships Ice chest + Ice pads 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.

Descripción general

H-D-Phe(4-Cl)-OH is a phenylalanine derivative.

Specifications

Sinónimos
EN300-366578 | NCGC00024889-01 | P-CHLORO-D-PHENYLALANINE | RSS1JQ7MES | AM82750 | AKOS016842281 | FS-2457 | (R)-2-Amino-3-(4-chlorophenyl)propionic Acid Hydrochloride | Z995228428 | d-p-chlorophenylalanine | NCGC00015255-01 | AC-5845 | (R)-4-Chlorophenyl
Especificaciones y pureza
≥95%
Condiciones de almacenamiento de almacenamiento
Store at -20°C
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥95%
Nombres e identificadores
Pubchem Sid504759805
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504759805
Sonrisas canónicasC1=CC(=CC=C1CC(C(=O)O)N)Cl
IUPAC Name(2R)-2-amino-3-(4-chlorophenyl)propanoic acid
InChIKeyNIGWMJHCCYYCSF-MRVPVSSYSA-N
INCHI1S/C9H10ClNO2/c10-7-3-1-6(2-4-7)5-8(11)9(12)13/h1-4,8H,5,11H2,(H,12,13)/t8-/m1/s1
Isómeros SMILES C1=CC(=CC=C1C[C@H](C(=O)O)N)Cl
Peso molecular 199.63
Reaxy-Rn 2805758
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2805758&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

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClaseCarboxylic 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 Phenylpropanoic acids  D-alpha-amino acids  Amphetamines and derivatives  Chlorobenzenes  Aralkylamines  Aryl chlorides  Amino acids  Monocarboxylic acids and derivatives  Carboxylic acids  Organopnictogen compounds  Organochlorides  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Phenylalanine or derivatives - 3-phenylpropanoic-acid - Alpha-amino acid - Amphetamine or derivatives - D-alpha-amino acid - Aralkylamine - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organohalogen compound - Organochloride - Primary aliphatic amine - Organonitrogen compound - Organooxygen compound - Primary amine - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Amine - Aromatic homomonocyclic compound
DescripciónThis 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
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NFKB1 Tclin Nuclear factor NF-kappa-B p105 subunit (1459 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KDM4E Tchem Lysine-specific demethylase 4D-like (40243 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Pkm Pyruvate kinase isozymes M1/M2 (66 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

9 results found

Lot NumberCertificate TypeFechaArticulo
E1529076Certificate of AnalysisJun 15, 2026 C131971
E2614185Certificate of AnalysisApr 29, 2026 C131971
E2614257Certificate of AnalysisApr 29, 2026 C131971
F2427430Certificate of AnalysisApr 02, 2026 C131971
F2427431Certificate of AnalysisApr 02, 2026 C131971
C2222524Certificate of AnalysisMar 13, 2026 C131971
C2222479Certificate of AnalysisOct 11, 2025 C131971
C2222495Certificate of AnalysisOct 11, 2025 C131971
F2427429Certificate of AnalysisJun 14, 2024 C131971
Propiedades químicas y físicas
Punto de fusión (°C)260℃
Peso molecular199.630 g/mol
XLogP3-0.500
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count3
Exact Mass199.04 Da
Monoisotopic Mass199.04 Da
Topological Polar Surface Area63.300 Ų
Heavy Atom Count13
Formal Charge0
Complexity178.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Calculadoras de soluciones
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