D-Phenylalaninol - ≥98% , CAS No.5267-64-1

CAS: 5267-64-1 Cat. No.: P100530 Peso molecular: 151.21 Beilstein Registry Number: 2208239 Número EC: 226-086-1
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
D(+)-Phenylalaninol;(R)-(+)-2-Amino-3-phenyl-1-propanol;D-Penylalaninol | D-phenyl alaninol | M04116 | UNII-A6QY3U3O3V | D-(+)-Phenylalaninol | EINECS 226-086-1 | A6QY3U3O3V | Z1157651018 | (2R)-2-amino-3-phenylpropan-1-ol | (R)-(+)-2-amino-3-phenylpropan
Storage
Argon charged,Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
P100530-1g
3

9,90US$

14,90US$
Guardar 5,00 US$ (33.56%)
5g
P100530-5g
3

11,90US$

17,90US$
Guardar 6,00 US$ (33.52%)
10g
P100530-10g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

14,90US$

22,90US$
Guardar 8,00 US$ (34.93%)
25g
P100530-25g
1

25,90US$

38,90US$
Guardar 13,00 US$ (33.42%)
100g
P100530-100g
2

90,90US$

136,90US$
Guardar 46,00 US$ (33.60%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Argon charged,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 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
D(+)-Phenylalaninol;(R)-(+)-2-Amino-3-phenyl-1-propanol;D-Penylalaninol | D-phenyl alaninol | M04116 | UNII-A6QY3U3O3V | D-(+)-Phenylalaninol | EINECS 226-086-1 | A6QY3U3O3V | Z1157651018 | (2R)-2-amino-3-phenylpropan-1-ol | (R)-(+)-2-amino-3-phenylpropan
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Argon charged, Room temperature
Enviado en
Normal
Pureza
≥98%
Nombres e identificadores
Pubchem Sid504760274
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504760274
Sonrisas canónicasC1=CC=C(C=C1)CC(CO)N
IUPAC Name(2R)-2-amino-3-phenylpropan-1-ol
InChIKeySTVVMTBJNDTZBF-SECBINFHSA-N
INCHI1S/C9H13NO/c10-9(7-11)6-8-4-2-1-3-5-8/h1-5,9,11H,6-7,10H2/t9-/m1/s1
Isómeros SMILES C1=CC=C(C=C1)C[C@H](CO)N
WGK Alemania 3
Número ONU 3259
Peso molecular 151.21
Beilstein 2208239
Reaxy-Rn 2208237
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2208237&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
SuperclassBenzenoids
ClaseBenzene and substituted derivatives
SubclassPhenethylamines
Intermediate Tree Nodes Not available
Direct ParentAmphetamines and derivatives
Alternative Parents Aralkylamines  1,2-aminoalcohols  Primary alcohols  Organopnictogen compounds  Monoalkylamines  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Amphetamine or derivatives - Aralkylamine - 1,2-aminoalcohol - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Primary alcohol - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Amine - Alcohol - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as amphetamines and derivatives. These are organic compounds containing or derived from 1-phenylpropan-2-amine.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





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.

7 results found

Lot NumberCertificate TypeFechaArticulo
I2103230Certificate of AnalysisJun 11, 2025 P100530
I2103233Certificate of AnalysisJun 11, 2025 P100530
I2103234Certificate of AnalysisJun 11, 2025 P100530
I2103235Certificate of AnalysisJun 11, 2025 P100530
A2607519Certificate of AnalysisJul 12, 2024 P100530
B2021071Certificate of AnalysisDec 19, 2023 P100530
J1526081Certificate of AnalysisJul 07, 2023 P100530
Propiedades químicas y físicas
SolubilidadSoluble in Dichloromethane, Ethyl Acetate, Methanol.
SensibilidadAir sensitive.
Rotación específica [α]23.5 ° (C=1.2, 1mol/L HCl)
Punto de ebullición (°C)122°C/4mmHg
Punto de fusión (°C)90-92°C
Peso molecular151.210 g/mol
XLogP30.700
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count3
Exact Mass151.1 Da
Monoisotopic Mass151.1 Da
Topological Polar Surface Area46.300 Ų
Heavy Atom Count11
Formal Charge0
Complexity99.700
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
Citations of This Product
Referencias
1. Chen Yuliang, Lai Kaijie, Cai Jinmi, Li Yicheng, Wang Haibo.  (2022)  Chiral Fluorescence Recognition by Anthracene Fluorescent Dyes ⊂ Water-Soluble Pillar[5] arene containing Phosphonic Acid Group (PWP[5]).  JOURNAL OF FLUORESCENCE,  32  (3): (983-992).  [PMID:35230565] [10.1007/s10895-022-02908-3]
2. Shanshan Wu, Qiumin Ye, Datong Wu, Yongxin Tao, Yong Kong.  (2020)  Enantioselective Recognition of Chiral Tryptophan with Achiral Glycine through the Strategy of Chirality Transfer.  ANALYTICAL CHEMISTRY,      [PMID:32786461] [10.1021/acs.analchem.0c02335]
3. Chen Xuanming, Hu Na, Wei Huifeng, Wang Haibo.  (2020)  Chiral Fluorescent Recognition by Naphthalimide.  JOURNAL OF FLUORESCENCE,  30  (3): (679-685).  [PMID:32367338] [10.1007/s10895-020-02539-6]
4. Jinhua Xu, Minghui Tang, Jinyu Zhang, Wenmin Zhang, Shiye Xie, Lan Zhang.  (2025)  Green and Controlled Synthesis of Copper-Based Tryptophan Flower-like Chiral Metal-Organic Framework for Enantioselective Recognition and Volatile Organic Compound Separation.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:40339186] [10.1016/j.chroma.2025.466020]
5. Jinhua Xu, Jinyu Zhang, Wenmin Zhang, Shiye Xie, Lan Zhang.  (2025)  Controllable synthesis of chiral hierarchical porous Co(OH)2 and its application in rapid chiral recognition and separation.  ANALYTICA CHIMICA ACTA,      [PMID:40480689] [10.1016/j.aca.2025.344212]
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