(R)-(+)-α-metilbencilaminas - ≥99%,≥98%(ee) , CAS No.3886-69-9

CAS: 3886-69-9 Cat. No.: M106714 Peso molecular: 121.18 Beilstein Registry Number: 2410916 Número EC: 223-423-4 PubChem CID: 643189
Disponible para pedir
GRADE & PURITY ≥99%,≥98%(ee)
Synonyms
(R)-(+)-1-Phenylethylamine | (R)-1-phenylethanamine | (1R)-1-phenylethanamine | (R)-(+)-alpha-Methylbenzylamine
Storage
Conservar a 2-8°C,cargado con argón
Shipped In
Hielo húmedo
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
25g
M106714-25g
2
11,90US$
100g
M106714-100g
3
25,90US$
500g
M106714-500g
3
85,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

≥99%,≥98%(ee) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Conservar a 2-8°C,cargado con argón Ships Hielo húmedo 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 25 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

la (R)-(+)-α-metilbencilamina es un reactivo de derivatización quiral útil y de alta calidad para todas las aplicaciones analíticas, específico para GC en el campo quiral. Se ha seleccionado especialmente para satisfacer los requisitos de los reactivos de derivatización para las determinaciones del exceso enantiomérico

Specifications

Sinónimos
(R)-(+)-1-Phenylethylamine | (R)-1-phenylethanamine | (1R)-1-phenylethanamine | (R)-(+)-alpha-Methylbenzylamine
Especificaciones y pureza
≥99%, ≥98%(ee)
Condiciones de almacenamiento de almacenamiento
Conservar a 2-8°C, cargado con argón
Enviado en
Hielo húmedo
Pureza
≥99%, ≥98%(ee)
Nombres e identificadores
Sonrisas canónicasC[C@@H](N)c1ccccc1
IUPAC Name(1R)-1-phenylethanamine
InChIKeyRQEUFEKYXDPUSK-SSDOTTSWSA-N
INCHI1S/C8H11N/c1-7(9)8-5-3-2-4-6-8/h2-7H,9H2,1H3/t7-/m1/s1
Isómeros SMILES C[C@H](C1=CC=CC=C1)N
WGK Alemania 3
PubChem CID 643189
Peso molecular 121.18
Beilstein 2410916

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 nitrogen compounds
ClaseOrganonitrogen compounds
SubclassAmines
Intermediate Tree Nodes Not available
Direct ParentAralkylamines
Alternative Parents Benzene and substituted derivatives  Organopnictogen compounds  Monoalkylamines  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Aralkylamine - Benzenoid - Monocyclic benzene moiety - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Primary aliphatic amine - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as aralkylamines. These are alkylamines in which the alkyl group is substituted at one carbon atom by an aromatic hydrocarbyl group.
External Descriptors 1-phenylethylamine
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
MAOB Tclin Monoamine oxidase B (8835 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PNMT Tchem Phenylethanolamine N-methyltransferase (540 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Grin1 Glutamate NMDA receptor (6467 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.

47 results found

Lot NumberCertificate TypeFechaArticulo
D2630519Certificate of AnalysisApr 20, 2026 M106714
D2628133Certificate of AnalysisApr 20, 2026 M106714
D2628132Certificate of AnalysisApr 20, 2026 M106714
D2628131Certificate of AnalysisApr 20, 2026 M106714
E2529025Certificate of AnalysisDec 31, 2024 M106714
A2509448Certificate of AnalysisDec 31, 2024 M106714
A2509451Certificate of AnalysisDec 31, 2024 M106714
A2509453Certificate of AnalysisDec 31, 2024 M106714
A2509454Certificate of AnalysisDec 31, 2024 M106714
A2509513Certificate of AnalysisDec 31, 2024 M106714
L2413402Certificate of AnalysisDec 07, 2024 M106714
L2413401Certificate of AnalysisDec 07, 2024 M106714
L2413398Certificate of AnalysisDec 07, 2024 M106714
L2413397Certificate of AnalysisDec 07, 2024 M106714
L2413344Certificate of AnalysisDec 07, 2024 M106714
K2412147Certificate of AnalysisNov 06, 2024 M106714
K2412146Certificate of AnalysisNov 06, 2024 M106714
K2412145Certificate of AnalysisNov 06, 2024 M106714
K2412144Certificate of AnalysisNov 06, 2024 M106714
K2412143Certificate of AnalysisNov 06, 2024 M106714
K2407395Certificate of AnalysisOct 14, 2024 M106714
K2407394Certificate of AnalysisOct 14, 2024 M106714
K2407393Certificate of AnalysisOct 14, 2024 M106714
H2513057Certificate of AnalysisOct 14, 2024 M106714
K2407392Certificate of AnalysisOct 14, 2024 M106714
I2410029Certificate of AnalysisSep 04, 2024 M106714
I2410027Certificate of AnalysisSep 04, 2024 M106714
I2410021Certificate of AnalysisSep 04, 2024 M106714
C2430101Certificate of AnalysisMar 18, 2024 M106714
B2418454Certificate of AnalysisJan 29, 2024 M106714
B2418453Certificate of AnalysisJan 29, 2024 M106714
B2418452Certificate of AnalysisJan 29, 2024 M106714
B2418451Certificate of AnalysisJan 29, 2024 M106714
B2418450Certificate of AnalysisJan 29, 2024 M106714
A2404216Certificate of AnalysisDec 21, 2023 M106714
A2404722Certificate of AnalysisDec 21, 2023 M106714
A2404723Certificate of AnalysisDec 21, 2023 M106714
A2404724Certificate of AnalysisDec 21, 2023 M106714
A2404738Certificate of AnalysisDec 21, 2023 M106714
A2404740Certificate of AnalysisDec 21, 2023 M106714
A2404739Certificate of AnalysisDec 21, 2023 M106714
I2224477Certificate of AnalysisJul 16, 2022 M106714
I2224492Certificate of AnalysisJul 16, 2022 M106714
I2224493Certificate of AnalysisJul 16, 2022 M106714
I2224494Certificate of AnalysisJul 16, 2022 M106714
E2326327Certificate of AnalysisNov 12, 2021 M106714
F23061504Certificate of AnalysisNov 12, 2021 M106714

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Propiedades químicas y físicas
SolubilidadSoluble in water (40 g/L).
SensibilidadMoisture sensitive; Air sensitive
Índice de refracción1.53
Rotación específica [α]39° (neat)
Punto de inflamación (°C)70°C
Punto de ebullición (°C)187-189 °C
Punto de fusión (°C)-10 °C
Peso molecular121.180 g/mol
XLogP31.200
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count1
Rotatable Bond Count1
Exact Mass121.089 Da
Monoisotopic Mass121.089 Da
Topological Polar Surface Area26.000 Ų
Heavy Atom Count9
Formal Charge0
Complexity74.600
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
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Qian Wang, Limei Sheng, Xuan Guo, Rong Chen, Chengjie Zhou, Fu Yang.  (2023)  Functionalized poly(ionic liquid)s bridging Pd NPs and lipase for highly efficient dynamic kinetic resolution of chiral amine.  APPLIED CATALYSIS A-GENERAL,      [PMID:] [10.1016/j.apcata.2023.119426]
2. Yuanyuan Li, Jinming Liu, Wei Li, Yingru Li, Wei Zhao, Haiquan Zhang.  (2023)  Enhancing the photothermal performance of graphene oxide by embedding perylene diimide radical anions/α-phenylethylamine hydrogen bonded complexes in graphene oxide films for solar water evaporation.  NEW JOURNAL OF CHEMISTRY,  47  (21): (10372-10380).  [PMID:] [10.1039/D3NJ01145C]
3. Shuang Jiang, Yuxin Song, Huimin Kang, Bin Li, Kunlong Yang, Guoxiang Xing, Ying Yu, Siyi Li, Peisheng Zhao, Tianyong Zhang.  (2021)  Ligand Exchange Strategy to Achieve Chiral Perovskite Nanocrystals with a High Photoluminescence Quantum Yield and Regulation of the Chiroptical Property.  ACS Applied Materials & Interfaces,      [PMID:34932328] [10.1021/acsami.1c18978]
4. Ruiheng Pan, Kai Wang, Zhi-Gang Yu.  (2021)  Magnetic-field manipulation of circularly polarized photoluminescence in chiral perovskites.  Materials Horizons,  (2): (740-747).  [PMID:34878471] [10.1039/D1MH01154E]
5. Xuejiao Yang, Yuhe Shen, Jiayu Liu, Yuefei Wang, Wei Qi, Rongxin Su, Zhimin He.  (2021)  Rational Design of Chiral Nanohelices from Self-Assembly of Meso-tetrakis (4-Carboxyphenyl) Porphyrin-Amino Acid Conjugates.  LANGMUIR,      [PMID:34711055] [10.1021/acs.langmuir.1c02213]
6. Youming Huang, Hongyi Chen, Wenting Zheng, Qingle Zeng.  (2020)  Cu2O-catalyzed C–S coupling of quaternary ammonium salts and sodium alkane-/arene-sulfinates.  TETRAHEDRON LETTERS,      [PMID:] [10.1016/j.tetlet.2020.152320]
7. Li-Xiao He, Chun-Rong Tian, Jun-Hui Zhang, Wen Xu, Bo Peng, Sheng-Ming Xie, Min Zi, Li-Ming Yuan.  (2019)  Chiral metal-organic cages used as stationary phase for enantioseparations in capillary electrochromatography.  ELECTROPHORESIS,      [PMID:31709552] [10.1002/elps.201900294]
8. Huajun Huang, Wantai Yang, Jianping Deng.  (2015)  Chiral, fluorescent microparticles constructed by optically active helical substituted polyacetylene: preparation and enantioselective recognition ability.  RSC Advances,  (33): (26236-26245).  [PMID:] [10.1039/C4RA16466K]
9. Yuan Wang, Mu-Sen Song, Jiaqi Zhao, Zhen Li, Tinglei Wang, Hai Wang, Hai-Yu Wang, Yu Wang.  (2024)  Chiral Perovskite Heterostructure Films of CsPbBr3 Quantum Dots and 2D Chiral Perovskite with Circularly Polarized Luminescence Performance and Energy Transfer.  ACS Nano,      [PMID:39120711] [10.1021/acsnano.4c06631]
10. Haotian Gao, Yu Chen, Ruxi Zhang, Rui Cao, Yong Wang, Yunfei Tian, Yin Xiao.  (2024)  Dual-ligand quasi-2D perovskites with chiral-induced spin selectivity for room temperature spin-LEDs.  Materials Horizons,  11  (12): (2906-2913).  [PMID:38567407] [10.1039/D3MH02029K]
11. Yizhen Zhang, Yu-Cai He, Cuiluan Ma.  (2024)  Efficient synthesis of vanillylamine through bioamination of lignin-derived vanillin by recombinant E. coli containing ω-transaminase from Caulobacter sp. D5 in dimethyl sulfoxide-water.  BIORESOURCE TECHNOLOGY,      [PMID:39321936] [10.1016/j.biortech.2024.131526]
12. Aumber Abbas, Qian Zhang, Jamal Kazmi, Ying Li, Wenbo Li, Waqas Ahmad, Chao Zou, Qijie Liang.  (2025)  Label-Free SERS Fingerprinting for Chiral Discrimination Using Chiral Two-Dimensional Superlattice.  NANO LETTERS,      [PMID:40763186] [10.1021/acs.nanolett.5c03047]
13. Shaolan Wang, Jinsheng Lin, Dan Li, Tianpei Huang, Wenquan Zhu, Wenbin Chen, Min Li, Weiyang Shen.  (2021)  Study of the isomeric Maillard degradants, glycosylamine and Amadori rearrangement products, and their differentiation via MS2 fingerprinting from collision-induced decomposition of protonated ions.  RAPID COMMUNICATIONS IN MASS SPECTROMETRY,  35  (9): (e9062).  [PMID:33533047] [10.1002/rcm.9062]
14. Jiaqi Zhao, Yuan Wang, Tinglei Wang, Yu Wang.  (2024)  Chiral defect-induced blue photoluminescence and circularly polarized luminescence of zero-dimensional Cs4PbBr6 perovskite nanocrystals.  Inorganic Chemistry Frontiers,  11  (14): (4424-4431).  [PMID:] [10.1039/D4QI01006J]
15. He Liu, Qian Gao, Kaiyue Zhang, Meng Xu, Hualei Wang, Dongzhi Wei.  (2024)  Combining binding pocket mutagenesis and substrate tunnel engineering to improve an (R)-selective transaminase for the efficient synthesis of (R)-3-aminobutanol.  BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS,      [PMID:39024977] [10.1016/j.bbrc.2024.150383]
16. Weijie Wu, Qingduan Li, Yue-Peng Cai, Songyang Yuan, Shengjian Liu.  (2025)  Dipole Regulation Ultrahigh-Oriented Two-Dimensional Perovskite Films for UV-Excited Secure Quick Response Codes.  ACS Applied Electronic Materials,      [PMID:] [10.1021/acsaelm.4c01851]
17. He Liu, Shixi Wang, Meng Xu, Kaiyue Zhang, Qian Gao, Hualei Wang, Dongzhi Wei.  (2024)  Engineering an (R)-selective transaminase for asymmetric synthesis of (R)-3-aminobutanol.  BIOORGANIC CHEMISTRY,      [PMID:38492494] [10.1016/j.bioorg.2024.107264]
18. Quanlin Chen, Mingwei Ge, Cong Geng, Jia Zhang, Linyue Gao, Zhuanzhuan Huang, Saike Wang, Yanxing Feng, Xinxin Yue, Saif M. H. Qaid, Xuewen Fu, Mei Wang, Yuanzhi Jiang, Mingjian Yuan.  (2025)  Manipulating perovskite structural asymmetry for high-performing self-powered full-stokes polarimetry.  Science Advances,  11  (9):   [PMID:40020053] [10.1126/sciadv.ads6123]
19. Mengyu Li, Wei Zhuang, Xia Meng, Wenxia Zhang, Keke Zhang, Zhenfu Wang.  (2025)  Tailoring microenvironments of metal-enzyme cascade catalysts for efficient DKR reaction of chiral amine.  JOURNAL OF CATALYSIS,      [PMID:] [10.1016/j.jcat.2025.116079]
20. Lei Shi, Yizhan Wang, Bao Li, Lixin Wu.  (2014)  Polyoxometalate complexes for oxidative kinetic resolution of secondary alcohols: unique effects of chiral environment, immobilization and aggregation.  DALTON TRANSACTIONS,  43  (24): (9177-9188).  [PMID:24810246] [10.1039/C4DT00742E]
21. Tao Zhou, Ran Tao, Yan Yu, Chong Li, Zhang Haonan, Jing-Ting Luo, Chen Fu, Fujian Ren, Yong Qing Fu.  (2025)  Chiral organic-inorganic hybrid perovskites synthesized using acoustofluidic closed system.  LAB ON A CHIP,      [PMID:40226971] [10.1039/D4LC01073F]
22. Yao Xu, Jian Li, Wenheng Xu, Xinlian Fan, Shuai Yang, Yao Yin, Jijie Zhu, Dawei Zhou, Linbo Feng, Chenyang Zha, Xiaoyong Wang, Yan Lv, Lin Wang.  (2025)  Elucidating Interfacial Carrier Transfer Dynamics for Circularly Polarized Emission in Self-Assembled Perovskite Heterostructures.  ACS Nano,      [PMID:40204749] [10.1021/acsnano.5c01450]
23. Yuan Yu, Xiangping Zhao, Chenghao Liu, Zhiyong Pang, Wei Qin.  (2025)  Chiral Orbital Modifying Dipolar Polarization and Recombination in Chiral Perovskites.  Journal of Physical Chemistry Letters,      [PMID:40473405] [10.1021/acs.jpclett.5c01227]
24. Junhua Di, Yizhen Zhang, Bright Uwse, Paul Arnaud Yao Koffi, Yu-Cai He, Cuiluan Ma.  (2026)  Site-directed mutagenesis to enhance thermostability of Caulobacter sp. D5 ω-transaminase for efficient bioamination of biobased aldehydes.  BIORESOURCE TECHNOLOGY,      [PMID:41611022] [10.1016/j.biortech.2026.134103]
25. Lewei Wang, Ru Zhang, Datong Wu, Wenrong Cai, Junyao Li, Yong Kong.  (2026)  High Performance Enantioselective Separation Facilitated by Charged Chiral Covalent Organic Framework Membrane.  ACS Applied Materials & Interfaces,      [PMID:] [10.1021/acsami.6c03050]
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