Styrene, 1,3-butadiene polymer

Product Information

Molecular Formula:
C12H14
Molecular Weight:
158.2426
Description
Rubber modifier. random copolymer.
Synonyms
1,3-BUTADIENE/STYRENE COPOLYMERS; BUTADIENE-STYRENE LATEX; BUTADIENE-STYRENE RESIN; PLIOLITE S-6B; PLIOLITE S-6H; POLY(STYRENE-CO-BUTADIENE); POLY(STYRENE/BUTADIENE); POLYSTYRENE-B-POLYBUTADIENE(1,2 ADDITION)
IUPAC Name
buta-1,3-dienestyrene
Canonical SMILES
C=CC=C.C=CC1=CC=CC=C1
InChI
InChI=1S/C8H8.C4H6/c1-2-8-6-4-3-5-7-81-3-4-2/h2-7H,1H23-4H,1-2H2
InChI Key
MTAZNLWOLGHBHU-UHFFFAOYSA-N
Boiling Point
145.2°C at 760 mmHg
Melting Point
-59°C
Flash Point
31.1°C
Purity
95%
Density
1.04 g/mL at 25 °C
Appearance
solid or viscous liquid, depending upon the degree of polymerisation
Application
Permitted for use as an inert ingredient in non-food pesticide products.
Storage
Store at room temperature
Tg
33-41°C
Stability
Stable. Combustible. Incompatible with strong oxidizing agents.

Safety Information

Hazards
Harmless-use normal precautions
Handling
Exercise normal care

Computed Properties

Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
2
Exact Mass
158.109550447 g/mol
Monoisotopic Mass
158.109550447 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
12
Formal Charge
0
Complexity
89.1
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
2
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
US-2016101218-A1 Copolymer membrane for high-dose chemotherapy delivery during transarterial chemoemblization 2014-10-10
US-2016168303-A1 Mono vinyl aromatic conjugated diene block copolymer and polymer composition comprising said block copolymer and a mono vinylarene acrylate copolymer 2013-07-08
US-2014162060-A1 Strippable adhesion composition and uses thereof 2012-12-06
US-9115298-B2 Strippable adhesion composition and uses thereof 2012-12-06
US-2015038654-A1 Emulsifier for emulsion polymerization and emulsion polymerization method using same 2011-12-20
US-9353195-B2 Emulsifier for emulsion polymerization and emulsion polymerization method using same 2011-12-20
US-2012277363-A1 Moisture-proof and insulating coating material and uses thereof 2011-04-26
US-9136038-B2 Moisture-proof and insulating coating material and uses thereof 2011-04-26
US-2013012646-A1 Styrene-based resin composition, and resin molded article comprising same 2010-03-19
US-8829104-B2 Styrene-based resin composition, and resin molded article comprising same 2010-03-19

Literatures

PMID Publication Date Title Journal
34324853 2021-09-25 1,3-Butadiene, styrene and selected outcomes among synthetic rubber polymer workers: Updated exposure-response analyses Chemico-biological interactions
26070419 2015-11-05 A comprehensive review of occupational and general population cancer risk: 1,3-Butadiene exposure-response modeling for all leukemia, acute myelogenous leukemia, chronic lymphocytic leukemia, chronic myelogenous leukemia, myeloid neoplasm and lymphoid neoplasm Chemico-biological interactions
22950720 2012-10-02 Utilizing carbon dioxide as a reaction medium to mitigate production of polycyclic aromatic hydrocarbons from the thermal decomposition of styrene butadiene rubber Environmental science & technology
22271599 2012-02-27 A novel thermotropic elastomer based on highly-filled LDH-SSB composites Macromolecular rapid communications
21600953 2011-08-01 Butadiene cancer exposure-response modeling: based on workers in the styrene-butadiene-rubber industry: total leukemia, acute myelogenous leukemia, chronic lymphocytic leukemia, and chronic myelogenous leukemia Regulatory toxicology and pharmacology : RTP
20868266 2010-10-01 1,3-Butadiene: I. Review of metabolism and the implications to human health risk assessment Critical reviews in toxicology
19215653 2009-02-01 Two-dimensional Raman correlation spectroscopy study of an emulsion copolymerization reaction process Applied spectroscopy
18935830 2008-07-01 Contribution made by multivariate curve resolution applied to gel permeation chromatography-Fourier transform infrared data for an in-depth characterization of styrene-butadiene rubber blends Applied spectroscopy
17889437 2008-05-01 Impacts of environmental conditions on the sorption of volatile organic compounds onto tire powder Journal of hazardous materials
18409655 2008-03-15 Investigation of mechanisms of polycyclic aromatic hydrocarbons (PAHs) initiated from the thermal degradation of styrene butadiene rubber (SBR) in N2 atmosphere Environmental science & technology
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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