ABS 3D printing filament - natural, diam. 2.85 mm , CAS No.9003-56-9

CAS: 9003-56-9 Cat. No.: A434459 EC Number: 618-371-8

GRADE & PURITY natural, diam. 2.85 mm

Synonyms

acrylonitrile-butadiene-styrene | butadiene styrene acrylonitrile | Q143496 | SCHEMBL15661 | XECAHXYUAAWDEL-UHFFFAOYSA-N | styrene-butadiene acrylonitrile | Acrylonitrile-butadiene-styrene terpolymer | buta-1,3-diene;prop-2-enenitrile;styrene | ABS | Acry

Storage

Room temperature

Overview

General Description

3DXTech ™ ABS is made in the USA using 100% virgin resin and colorants - precision extruded onto 1kg reels (2.2 lbs.). The filament is then vacuum-sealed with desiccant to protect it from moisture.

Specifications

Synonyms

acrylonitrile-butadiene-styrene | butadiene styrene acrylonitrile | Q143496 | SCHEMBL15661 | XECAHXYUAAWDEL-UHFFFAOYSA-N | styrene-butadiene acrylonitrile | Acrylonitrile-butadiene-styrene terpolymer | buta-1, 3-diene;prop-2-enenitrile;styrene | ABS | Acry

Specifications & Purity

natural, diam. 2.85 mm

Legal Information

Product of 3DXTech ™ 3DXTech is a trademark of 3DXTech

Storage

Room temperature

Names and Identifiers

• Canonical Smiles: C=CC=C.C=CC#N.C=CC1=CC=CC=C1
• IUPAC Name: buta-1,3-diene;prop-2-enenitrile;styrene
• InChIKey: XECAHXYUAAWDEL-UHFFFAOYSA-N
• INCHI: 1S/C8H8.C4H6.C3H3N/c1-2-8-6-4-3-5-7-8;1-3-4-2;1-2-3-4/h2-7H,1H2;3-4H,1-2H2;2H,1H2
• Isomeric SMILES: C=CC=C.C=CC#N.C=CC1=CC=CC=C1
• Reaxy-Rn: 14668688
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=14668688&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Class Benzene and substituted derivatives
      • Subclass Styrenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Class: Benzene and substituted derivatives
• Subclass: Styrenes
• Intermediate Tree Nodes: Not available
• Direct Parent: Styrenes
• Alternative Parents: Aromatic hydrocarbons Cyclic olefins
• Molecular Framework: Not available
• Substituents: Styrene - Aromatic hydrocarbon - Cyclic olefin - Unsaturated hydrocarbon - Olefin - Hydrocarbon - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as styrenes. These are organic compounds containing an ethenylbenzene moiety.
• External Descriptors: Not available

Data sources

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

Chemical and Physical Properties

• Molecular Weight: 211.300 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 211.136 Da
• Monoisotopic Mass: 211.136 Da
• Topological Polar Surface Area: 23.800 Ų
• Heavy Atom Count: 16
• Formal Charge: 0
• Complexity: 144.000
• 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: 3

XLogP3

References

1. He Guo, Xiaomeng Cheng, Hongping Li, Jun Li, Jinjin Wei, Chongyang Feng.  (2020)  Synthesis, micellar structures and emission mechanisms of an AIE and DDED-featured fluorescent pH- and thermo-meter.  RSC Advances,  10  (40): (23532-23542).  [PMID:35517342] [10.1039/D0RA01000F]

2. Yesu Zhang, Yanhong Quan, Jun Ren.  (2024)  Influence of the surface SO3H groups on the performance of activated carbon catalyst for ethanolysis of furfuryl alcohol to ethyl levulinate.  Molecular Catalysis,      [PMID:] [10.1016/j.mcat.2024.114363]

3. Jinbao Huang, Liming Tai, Shi Yan, Sijia Li, Hao Cheng, Hong Wang, Yu Lv, Wenjing Duan, Xinsheng Li.  (2025)  Theoretical and experimental research on degradation mechanism of acrylonitrile-butadiene-styrene copolymer (ABS).  JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS,      [PMID:] [10.1016/j.jaap.2025.107541]