(S)-(-)-1-Phenylethylamine - 10mM in DMSO , CAS No.2627-86-3

CAS: 2627-86-3 Cat. No.: S422929 Molecular Weight: 121.18 Beilstein Registry Number: 2204907 EC Number: 220-098-0
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GRADE & PURITY 10mM in DMSO
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 -80°C
Shipped In
Dry ice packs + Cold packs
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Size
Status
Price
Qty
1ml
S422929-1ml
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs 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 19 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Used in a one-pot, multi-component synthesis of a highly substituted, chiral pyrrole

Specifications

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
Specifications & Purity
10mM in DMSO
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers
Canonical SmilesCC(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
Isomeric SMILES C[C@@H](C1=CC=CC=C1)N
WGK Germany 1
RTECS DP5775000
UN Number 2922
Packing Group II
Molecular Weight 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.

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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 nitrogen compounds
ClassOrganonitrogen 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
DescriptionThis 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
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
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
Associated Targets(non-human)
Bos taurus (956 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Grin1 Glutamate NMDA receptor (6467 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:
Chemical and Physical Properties
SensitivityAir and moisture sensitive
Refractive Index1.526
Specific Rotation[α]-39 ° (neat)
Flash Point(°F)158 °F
Flash Point(°C)70 °C
Boil Point(°C)187°C
Melt Point(°C)-10°C
Molecular Weight121.180 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
Documents & Articles
Citations of This Product
References
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. 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]
8. 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]
9. 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]
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]
Solution Calculators
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