average Mₙ ~3,800, acrylonitrile 8-12wt. % for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping
Room temperature Ships Normal 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Overview
Enhances impact strength, thermal shock, peel strength and crack resistance of epoxy compositions.
Description
Component of epoxy-based adhesives, composites and coatings. Intermediate in corrosion-resistant vinyl esters, acrylated epoxies used in radiation curing and photopolymer printing plates.
Specifications
Synonyms
POLY(BUTADIENE-CO-ACRYLONITRILE), DICARBOXY TERMINATED | SCHEMBL22216 | 2-Propenenitrile, polymer with 1, 3-butadieneOTHER CA INDEX NAMES:1, 3-Butadiene, polymer with 2-propenenitrile | Poly(acrylonitrile-co-butadiene) | butadiene-acrylonitrile | ACRYLONITR
Specifications & Purity
average Mₙ ~3, 800, acrylonitrile 8-12wt. %
Storage
Room temperature
Shipped In
Normal
Names and Identifiers
Canonical Smiles
C=CC=C.C=CC#N
IUPAC Name
buta-1,3-diene;prop-2-enenitrile
InChIKey
NTXGQCSETZTARF-UHFFFAOYSA-N
INCHI
1S/C4H6.C3H3N/c1-3-4-2;1-2-3-4/h3-4H,1-2H2;2H,1H2
Isomeric SMILES
C=CC=C.C=CC#N
PubChem CID
155116
Documentation
📋 Safety Data Sheet (SDS)
Comprehensive hazard, handling, storage, and regulatory compliance document.
This compound belongs to the class of organic compounds known as nitriles. These are compounds having the structure RC#N; thus C-substituted derivatives of hydrocyanic acid, HC#N.
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.
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