(S)-(-)-1-Phenylethylamine - ≥99%(GC) , CAS No.2627-86-3

CAS: 2627-86-3 Cat. No.: M105679 Peso molecular: 121.18 Beilstein Registry Number: 2204907 Número EC: 220-098-0
Disponible para pedir
GRADE & PURITY ≥99%(GC)
Synonyms
(1 S)-1-phenylethanamine | (s)-alpha-methylbenzyl amine | .ALPHA.-METHYLBENZYLAMINE (-)-FORM [MI] | RQEUFEKYXDPUSK-ZETCQYMHSA-N | (s)-(-)-phenethylamine | (S)-alpha-Methylbenzylamine | (S)-alpha-methyl-benzylamine | AC-8774 | L-(-)-alpha-Phenylethylamine
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1ml
M105679-1ml
2
9,90US$
5ml
M105679-5ml
4
9,90US$
25ml
M105679-25ml
5
10,90US$
100ml
M105679-100ml
5
30,90US$
500ml
M105679-500ml
7
81,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

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

🌡

Storage & shipping

Store at 2-8°C,Argon charged Ships Wet ice 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 19 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
(1 S)-1-phenylethanamine | (s)-alpha-methylbenzyl amine | .ALPHA.-METHYLBENZYLAMINE (-)-FORM [MI] | RQEUFEKYXDPUSK-ZETCQYMHSA-N | (s)-(-)-phenethylamine | (S)-alpha-Methylbenzylamine | (S)-alpha-methyl-benzylamine | AC-8774 | L-(-)-alpha-Phenylethylamine
Especificaciones y pureza
≥99%(GC)
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C, Argon charged
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥99%(GC)
Nombres e identificadores
Pubchem Sid488185169
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488185169
Sonrisas canónicasCC(C1=CC=CC=C1)N
IUPAC Name(1S)-1-phenylethanamine
InChIKeyRQEUFEKYXDPUSK-ZETCQYMHSA-N
INCHI1S/C8H11N/c1-7(9)8-5-3-2-4-6-8/h2-7H,9H2,1H3/t7-/m0/s1
Isómeros SMILES C[C@@H](C1=CC=CC=C1)N
WGK Alemania 1
RTECS DP5775000
Número ONU 2922
Grupo de embalaje II
Peso molecular 121.18
Beilstein 2204907
Reaxy-Rn 636127
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=636127&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 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)
Bos taurus (956 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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.

24 results found

Lot NumberCertificate TypeFechaArticulo
D2623851Certificate of AnalysisApr 28, 2026 M105679
B2226303Certificate of AnalysisDec 12, 2025 M105679
D2101348Certificate of AnalysisJan 13, 2025 M105679
D2101350Certificate of AnalysisJan 13, 2025 M105679
J2320517Certificate of AnalysisOct 10, 2023 M105679
J2320516Certificate of AnalysisOct 10, 2023 M105679
K1928212Certificate of AnalysisSep 11, 2023 M105679
G2510013Certificate of AnalysisJun 29, 2023 M105679
G2507034Certificate of AnalysisJun 29, 2023 M105679
G2326568Certificate of AnalysisJun 29, 2023 M105679
G2326559Certificate of AnalysisJun 29, 2023 M105679
F2604005Certificate of AnalysisJun 29, 2023 M105679
G2326328Certificate of AnalysisJun 29, 2023 M105679
G2326330Certificate of AnalysisJun 29, 2023 M105679
G2326335Certificate of AnalysisJun 29, 2023 M105679
E2309710Certificate of AnalysisDec 03, 2022 M105679
B2525066Certificate of AnalysisDec 03, 2022 M105679
E2309727Certificate of AnalysisDec 03, 2022 M105679
E2309724Certificate of AnalysisDec 03, 2022 M105679
E2309718Certificate of AnalysisDec 03, 2022 M105679
E2309715Certificate of AnalysisDec 03, 2022 M105679
E2309703Certificate of AnalysisDec 03, 2022 M105679
B2226306Certificate of AnalysisDec 21, 2021 M105679
B2226302Certificate of AnalysisDec 21, 2021 M105679

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Propiedades químicas y físicas
SolubilidadSlightly miscible with water.
SensibilidadAir and moisture sensitive
Índice de refracción1.526
Rotación específica [α]-39 ° (neat)
Punto de inflamación (°F)158 °F
Punto de inflamación (°C)70 °C
Punto de ebullición (°C)187°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. Bing Tang, Shixun Wang, Haochen Liu, Nanli Mou, Arsenii S. Portniagin, Peigang Chen, Ye Wu, Xiaoqing Gao, Dangyuan Lei, Andrey L. Rogach.  (2023)  Chiral Ligand-Induced Inversion and Tuning of Excitonic Optical Activity in Intrinsically Chiral CsPbBr3 Perovskite Nanoplatelets.  Advanced Optical Materials,      [PMID:] [10.1002/adom.202301524]
3. Zhangchuan Wen, Rong Lu, Fan Gu, Kai Zheng, Lijie Zhang, Huile Jin, Yihuang Chen, Shun Wang, Shuang Pan.  (2022)  Enabling Efficient Blue-Emissive Circularly Polarized Luminescence by In Situ Crafting of Chiral Quasi-2D Perovskite Nanosheets within Polymer Nanofibers.  ADVANCED FUNCTIONAL MATERIALS,  33  (7): (2212095).  [PMID:] [10.1002/adfm.202212095]
4. Datong Wu, Cong Ma, Ting Wan, Pengfen Zhu, Yong Kong.  (2022)  Strategies to synthesize a chiral helical polymer accompanying with two stereogenic centers for chiral electroanalysis.  ANALYTICA CHIMICA ACTA,      [PMID:35473883] [10.1016/j.aca.2022.339810]
5. Xu Zhu, Ruiying Wang, Yafang Ge, Yingling Dong, Benlai Wu.  (2022)  A new two-dimensional homochiral cadmium(II) coordination polymer: synthesis, structure determination, optical properties, and fluorescent sensing.  JOURNAL OF COORDINATION CHEMISTRY,      [PMID:] [10.1080/00958972.2021.2007891]
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. 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]
8. 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]
9. Zhao Ke, Tan Liang-Xiao, Gao Ning, Sun Jian-Ke.  (2025)  Ionic organic cage as a versatile platform for immobilizing chemical and enzymatic sites for chemoenzymatic catalysis.  Nature Communications,  16  (1): (1-15).  [PMID:40592833] [10.1038/s41467-025-60292-5]
10. 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]
11. 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]
12. 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]
13. 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]
14. 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]
15. Chang Gu, Tao Wang, Xian Qin, Xiaogang Liu.  (2025)  Halogen Bonding-Enabled Stabilization of Copper(I) Cluster Scintillators in Aqueous Environments.  Advanced Optical Materials,      [PMID:] [10.1002/adom.202501022]
16. 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]
17. 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]
18. Jie Bai, Yongchun Huang, Yuling Zhao, Lirong Zhang, Fuli Zhu, Yixizhuoma, Yuxin Weng, Shoude Zhang.  (2026)  Determination of the monosaccharide types and absolute configurations in polysaccharides with (S)-(-)-1-phenylethylamine based on UPLC-MS/MS.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:41638272] [10.1016/j.ijbiomac.2026.150674]
19. 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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