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2-(4-Aminophenyl)ethylamine - 97%, high purity , CAS No.13472-00-9

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2-(4-Aminophenyl)ethylamine - 97%, high purity , CAS No.13472-00-9

1 Citations

COA

Grade & Purity:

≥97%

Cas Number: 13472-00-9
Molecular Weight: 136.2
Beilstein Registry Number: 1099910
MDL number: MFCD00008194
PubChem CID: 72895
PubChem SID: 504754678

In stock

Item Number

A151503

Grouped product items
SKU	Size	Availability	Price
A151503-1g	1g	3	$39.90
A151503-5g	5g	1	$150.90
A151503-25g	25g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$516.90
A151503-100g	100g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$1,860.90

View related series

Nitrogenous compounds (2445) Non heterocyclic block (8163)

Basic Description

Synonyms	4-Amino-.beta.-phenylethylamine \| 4-AMINOPHENYL ETHYLAMINE \| 1-Amino-2-(4-aminophenyl)ethane \| AMY31595 \| 4-aminoethylaniline \| 4-(2-Aminoethyl)aniline \| 4-(2-Amino-ethyl)-aniline \| 4-(2-Aminoethyl)aniline, 97% \| FT-0650483 \| 2-(4-Aminophenyl)ethylamine \|
Specifications & Purity	≥97%
Storage Temp	Protected from light,Argon charged
Shipped In	Normal
Product Description	4-(2-Aminoethyl)aniline undergoes coupling with carbohydrates by reductive amination to yield modified carbohydrates. 4-(2-Aminoethyl)aniline has been used in chemical modification of silk fibroin to tailor the overall hydrophilicity and structure of silk. It has been used as reagent in polycondensation reactions.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Benzene and substituted derivatives
    - Subclass Phenethylamines

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Benzene and substituted derivatives
Subclass	Phenethylamines
Intermediate Tree Nodes	Not available
Direct Parent	Phenethylamines
Alternative Parents	Aniline and substituted anilines 2-arylethylamines Aralkylamines Organopnictogen compounds Monoalkylamines Hydrocarbon derivatives
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Phenethylamine - 2-arylethylamine - Aniline or substituted anilines - Aralkylamine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Primary aliphatic amine - Amine - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as phenethylamines. These are compounds containing a phenethylamine moiety, which consists of a phenyl group substituted at the second position by an ethan-1-amine.
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

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	504754678
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504754678
IUPAC Name	4-(2-aminoethyl)aniline
INCHI	InChI=1S/C8H12N2/c9-6-5-7-1-3-8(10)4-2-7/h1-4H,5-6,9-10H2
InChIKey	LNPMZQXEPNWCMG-UHFFFAOYSA-N
Smiles	C1=CC(=CC=C1CCN)N
Isomeric SMILES	C1=CC(=CC=C1CCN)N
WGK Germany	3
Molecular Weight	136.2
Beilstein	1099910
Reaxy-Rn	1099913
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1099913&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.

8 results found

Lot Number	Certificate Type	Date	Item
H2322129	Certificate of Analysis	Jan 10, 2023	A151503
H2322140	Certificate of Analysis	Jan 10, 2023	A151503
H2322128	Certificate of Analysis	Jan 10, 2023	A151503
K1809111	Certificate of Analysis	Sep 15, 2022	A151503
K1809110	Certificate of Analysis	Sep 15, 2022	A151503
H2205716	Certificate of Analysis	Jun 15, 2022	A151503
H2205717	Certificate of Analysis	Jun 15, 2022	A151503
H2205718	Certificate of Analysis	Jun 15, 2022	A151503

Chemical and Physical Properties

Solubility	Insoluble in water.
Sensitivity	Air sensitive ；Light sensitive
Refractive Index	1.59
Flash Point(°F)	235.4 °F
Flash Point(°C)	113 °C
Boil Point(°C)	142 °C
Melt Point(°C)	28 °C
Molecular Weight	136.190 g/mol
XLogP3	-0.200
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	2
Exact Mass	136.1 Da
Monoisotopic Mass	136.1 Da
Topological Polar Surface Area	52.000 Å²
Heavy Atom Count	10
Formal Charge	0
Complexity	85.300
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
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. Chanjuan Liu, Luyao Yang, Qingfeng Niu, Guangli Yu, Guoyun Li. (2022) Carbohydrate microarrays fabricated on poly(2-methylacrylic acid)-based substrates for analysis of carbohydrate–protein interactions. NEW JOURNAL OF CHEMISTRY, 46 (9): (4300-4306).

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