Determine the necessary mass, volume, or concentration for preparing a solution.
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 19 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Used in a one-pot, multi-component synthesis of a highly substituted, chiral pyrrole
| Canonical Smiles | CC(C1=CC=CC=C1)N |
|---|---|
| IUPAC Name | (1S)-1-phenylethanamine |
| InChIKey | RQEUFEKYXDPUSK-ZETCQYMHSA-N |
| INCHI | 1S/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= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic nitrogen compounds |
| Class | Organonitrogen compounds |
| Subclass | Amines |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Aralkylamines |
| Alternative Parents | Benzene and substituted derivatives Organopnictogen compounds Monoalkylamines Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Aralkylamine - Benzenoid - Monocyclic benzene moiety - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Primary aliphatic amine - Aromatic homomonocyclic compound |
| Description | This 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 |
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| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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| Sensitivity | Air and moisture sensitive |
|---|---|
| Refractive Index | 1.526 |
| 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 Weight | 121.180 g/mol |
| XLogP3 | 1.200 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 1 |
| Exact Mass | 121.089 Da |
| Monoisotopic Mass | 121.089 Da |
| Topological Polar Surface Area | 26.000 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 74.600 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 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] |