4-Aminostyrene(P4VA) - ≥95%(T) , CAS No.1520-21-4

CAS: 1520-21-4 Cat. No.: A151485 Molecular Weight: 119.17 EC Number: 216-185-8
AVAILABLE TO ORDER
GRADE & PURITY ≥95%(T)
Synonyms
p-Aminostyrene | 4-vinylphenylamine | P4VA
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
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Size
Status
Price
Qty
250mg
A151485-250mg
3
$14.90
1g
A151485-1g
3
$58.90
5g
A151485-5g
1
$201.90
25g
A151485-25g
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$341.90
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Why this grade

≥95%(T) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at 2-8°C,Argon charged Ships Wet ice 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 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

4-Vinylaniline (4-VAn) is a primary amine surfactant.
4-VAn undergoes graft copolymerization with poly(tetrafluoroethylene) (PTFE) and Si surface, followed by oxidative copolymerization with aniline. Thus, it renders PTFE and Si surface conductive.4-VAn is coupled with hydrogen terminated Si surfaces for electroless metal and synthetic metal deposition.Palladium(II) schiff base complexes derived from Allylamine and vinylaniline has been reported. It also acts as a second surfactant for coating nanomagnetic particles. It is used in functionalization of single-walled carbon nanotube through solvent free functionalization.

General description
4-Vinylaniline is a vinyl-substituted aromatic amine that is widely used as a crosslinking agent in the production of resins, adhesives, and coatings, enhancing their mechanical properties and chemical resistance. It can be polymerized by methods like radical polymerization, cationic polymerization, or oxidative polymerization to form poly(4-vinylaniline) or P4VA. 4- Vinylaniline can be selectively polymerized or chemically modified to respond to specific analytes or stimuli, allowing the development of conductive polymers for biosensors.
Application
4-Vinylaniline can be used as:
A monomer to prepare electrically conductive polyvinylaniline/polyaniline (PVAN/PANI) bilayer for surface modification of bacterial cellulose (BC) nanofibril network. This material can be utilized as an electrochemical biosensor for nerve regenerative medicine.
To functionalize carbon nanodots for in vivo fluorometric biosensors, for the detection of mercury and cysteine.
As a precursor to prepare conductive and biocompatible hydrogels forwound healing applications.

Specifications

Synonyms
p-Aminostyrene | 4-vinylphenylamine | P4VA
Specifications & Purity
≥95%(T)
Storage
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.
Purity
≥95%(T)
Names and Identifiers
Canonical SmilesC=CC1=CC=C(C=C1)N
IUPAC Name4-ethenylaniline
InChIKeyLBSXSAXOLABXMF-UHFFFAOYSA-N
INCHI1S/C8H9N/c1-2-7-3-5-8(9)6-4-7/h2-6H,1,9H2
Isomeric SMILES C=CC1=CC=C(C=C1)N
Molecular Weight 119.17
Reaxy-Rn 2204173
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2204173&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
SuperclassBenzenoids
ClassBenzene and substituted derivatives
SubclassStyrenes
Intermediate Tree Nodes Not available
Direct ParentStyrenes
Alternative Parents Aniline and substituted anilines  Primary amines  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Aniline or substituted anilines - Styrene - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Amine - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as styrenes. These are organic compounds containing an ethenylbenzene moiety.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





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.

15 results found

Lot NumberCertificate TypeDateItem
I2526149Certificate of AnalysisOct 15, 2025 A151485
I2526150Certificate of AnalysisOct 15, 2025 A151485
I2526151Certificate of AnalysisOct 15, 2025 A151485
I2526199Certificate of AnalysisOct 15, 2025 A151485
F2622084Certificate of AnalysisAug 12, 2025 A151485
G2531162Certificate of AnalysisAug 12, 2025 A151485
G2531163Certificate of AnalysisAug 12, 2025 A151485
G2531164Certificate of AnalysisAug 12, 2025 A151485
H2511718Certificate of AnalysisAug 12, 2025 A151485
K2112280Certificate of AnalysisAug 12, 2025 A151485
C2412073Certificate of AnalysisMar 20, 2024 A151485
C2426034Certificate of AnalysisMar 20, 2024 A151485
I2425345Certificate of AnalysisMar 20, 2024 A151485
C2412072Certificate of AnalysisNov 01, 2021 A151485
J2331012Certificate of AnalysisNov 01, 2021 A151485

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Chemical and Physical Properties
SolubilitySoluble in Methanol,Benzene,Acetone
Sensitivitylight & heat & air sensitive
Refractive Indexn20/D 1.626
Boil Point(°C)213-214 °C
Melt Point(°C)21 °C
Molecular Weight119.160 g/mol
XLogP31.800
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count1
Rotatable Bond Count1
Exact Mass119.073 Da
Monoisotopic Mass119.073 Da
Topological Polar Surface Area26.000 Ų
Heavy Atom Count9
Formal Charge0
Complexity90.700
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
References
1. Xi Yu, Feng Lin, Pengqiang Li, Shifeng Yan, Kunxi Zhang, Wenguo Cui, Jingbo Yin.  (2022)  Porous scaffolds with enzyme-responsive Kartogenin release for recruiting stem cells and promoting cartilage regeneration.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2022.137454]
2. Ye Wei, Xuejie Yu, Ping Wang, Yuanyuan Yu, Jiugang Yuan, Qiang Wang, Xuerong Fan.  (2021)  Antibacterial Functionalization of Silk Fabrics following in Situ Coloring with Diazo Salts.  Journal of Natural Fibers,      [PMID:] [10.1080/15440478.2019.1701605]
3. Yujie Wang, Jiaying Liu, Yongbo Cui, Meng Liu, Wenxia Chen, Wei Wei, Haifeng Lu, Dongyun Han.  (2025)  Amorphous CoS polyhedron endow efficient electrocatalytic semi-hydrogenation of acetylene.  Materials Today Communications,      [PMID:] [10.1016/j.mtcomm.2025.112431]
Solution Calculators
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