Basic Description

Synonyms	AI3-26858 \| (1S)-1-naphthalen-1-ylethanamine \| 1-Naphthalenemethanamine, alpha-methyl-, (.alpha.S)- \| (1S)-(-)-1-(Naphth-1-yl)ethylamine \| (S)-(-)-alpha-(1-Naphthyl)ethylamine \| L-.alpha.-(.alpha.-Naphthyl)ethylamine
Specifications & Purity	≥99%
Storage Temp	Store at 2-8°C,Argon charged
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	(S)-(-)-1-(1-Naphthyl)ethylamine, (S)-(-)-1-(1-Naphthyl)ethylamine is used in the asymmetric synthesis of α-cyanocarboxylates. Also used in the synthesis of chiral imadazolin-2-ylidene ligands used in organometallic catalysis. Chiral/Asymmetric synthesis.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Naphthalenes

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Naphthalenes
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Naphthalenes
Alternative Parents	Aralkylamines Organopnictogen compounds Monoalkylamines Hydrocarbon derivatives
Molecular Framework	Aromatic homopolycyclic compounds
Substituents	Naphthalene - Aralkylamine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Primary aliphatic amine - Amine - Aromatic homopolycyclic compound
Description	This compound belongs to the class of organic compounds known as naphthalenes. These are compounds containing a naphthalene moiety, which consists of two fused benzene rings.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

Pubchem Sid	488183777
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488183777
IUPAC Name	(1S)-1-naphthalen-1-ylethanamine
INCHI	InChI=1S/C12H13N/c1-9(13)11-8-4-6-10-5-2-3-7-12(10)11/h2-9H,13H2,1H3/t9-/m0/s1
InChIKey	RTCUCQWIICFPOD-VIFPVBQESA-N
Smiles	CC(C1=CC=CC2=CC=CC=C21)N
Isomeric SMILES	C[C@@H](C1=CC=CC2=CC=CC=C21)N
WGK Germany	3
RTECS	QJ6963000
Molecular Weight	171.24
Beilstein	220802
Reaxy-Rn	2208023
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2208023&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

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.

23 results found

Lot Number	Certificate Type	Date	Item
E2515521	Certificate of Analysis	Apr 09, 2025	N122375
E2515497	Certificate of Analysis	Apr 09, 2025	N122375
E2515496	Certificate of Analysis	Apr 09, 2025	N122375
J2424869	Certificate of Analysis	Apr 13, 2024	N122375
J2308588	Certificate of Analysis	Sep 13, 2023	N122375
L2427214	Certificate of Analysis	Sep 13, 2023	N122375
J2308589	Certificate of Analysis	Sep 13, 2023	N122375
J2308590	Certificate of Analysis	Sep 13, 2023	N122375
A2415195	Certificate of Analysis	Sep 13, 2023	N122375
J2425228	Certificate of Analysis	Sep 13, 2023	N122375
F2404081	Certificate of Analysis	Sep 13, 2023	N122375
J2308587	Certificate of Analysis	Sep 13, 2023	N122375
J2308591	Certificate of Analysis	Sep 13, 2023	N122375
G23131068	Certificate of Analysis	Apr 18, 2023	N122375
G23131067	Certificate of Analysis	Apr 18, 2023	N122375
G23131070	Certificate of Analysis	Apr 18, 2023	N122375
G23131080	Certificate of Analysis	Apr 18, 2023	N122375
G23131071	Certificate of Analysis	Apr 18, 2023	N122375
G23131064	Certificate of Analysis	Apr 18, 2023	N122375
G23131069	Certificate of Analysis	Apr 18, 2023	N122375
G23131083	Certificate of Analysis	Apr 18, 2023	N122375
G23131081	Certificate of Analysis	Apr 18, 2023	N122375
G23131082	Certificate of Analysis	Apr 18, 2023	N122375

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Chemical and Physical Properties

Solubility	Soluble in chloroform, ethanol.
Sensitivity	Heat sensitive;Moisture sensitive;Air sensitive
Refractive Index	1.623
Specific Rotation[α]	-80.5°C
Flash Point(°C)	>110 ℃
Boil Point(°C)	153°C/11mmHg
Molecular Weight	171.240 g/mol
XLogP3	2.800
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	1
Exact Mass	171.105 Da
Monoisotopic Mass	171.105 Da
Topological Polar Surface Area	26.000 Å²
Heavy Atom Count	13
Formal Charge	0
Complexity	167.000
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

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Nan Jiang, Xiaotong Du, Liangyu Zheng. (2023) Highly efficient synthesis of chiral lactams by using a ω-transaminase from Bacillus megaterium and its mutant enzymes. Molecular Catalysis, 547 (113364).
2. Zhengwei Yang, Haolin Lu, Yu Zhang, Baipeng Yin, Hong Wang, Sehrish Gull, Wei Qin, Yongsheng Chen, Jiannian Yao, Chuang Zhang, Guankui Long. (2024) A Universal Strategy to Enhance Circularly Polarized Luminescence Brightness in Chiral Perovskites. Laser & Photonics Reviews, (2400040).

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SKU	Size	Availability	Price
N122375-1g	1g	5	$9.90
N122375-5g	5g	4	$29.90
N122375-10g	10g	3	$39.90
N122375-25g	25g	4	$79.90
N122375-100g	100g	1	$209.90

(S)-(-)-1-(1-Naphthyl)ethylamine - 99%, high purity , CAS No.10420-89-0