Skip to Content
Merck
All Photos(2)

Documents

Safety Information

466867

Sigma-Aldrich

Polybutadiene, predominantly 1,2-addition

approx. 90% 1,2-vinyl

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
[CH2CH(CH=CH2)]n
CAS Number:
9003-17-2
MDL number:
MFCD00084398
UNSPSC Code:
12162002
PubChem Substance ID:
24870367
NACRES:
NA.23

refractive index

n20/D 1.5002 (lit.)

viscosity

30-100 poise(45 °C)(lit.)

transition temp

Tg −30 °C

density

0.86 g/mL at 25 °C (lit.)

SMILES string

C=CC=C

InChI

1S/C4H8/c1-3-4-2/h3-4H,1-2H3/b4-3+

InChI key

IAQRGUVFOMOMEM-ONEGZZNKSA-N

Application

  • Transforming Polybutadiene with Tetrazine Click Chemistry into Antioxidant Foams That Fluoresce with Oxidation: This research uses tetrazine click chemistry to modify polybutadiene, enhancing its properties to create antioxidant foams that respond to oxidation with fluorescence, demonstrating innovative ways to utilize 1,2-addition polybutadiene (RE Bagge et al., 2017).
  • Isoxazoline-based porous polymer for the highly effective adsorption of 2,4,6-trinitrotoluene (TNT): Catalyst-free click polymerization between an in situ generated nitrile oxide with polybutadiene. This article explores the enhancement of polybutadiene′s adsorptive properties for environmental cleanup applications, emphasizing how its structural characteristics affect performance (H Deng et al., 2020).
  • Modification of polybutadiene with trifluoromethyl and clickable azide groups in one shot: This paper describes the simultaneous introduction of trifluoromethyl and azide functional groups into polybutadiene, showcasing the versatility of 1,2-addition polybutadiene in chemical modifications (S Wang et al., 2021).

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

466867-250ML:
466867-BULK:
466867-100ML:
466867-VAR:

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Deniz Turgut et al.
PloS one, 5(12), e15551-e15551 (2010-12-24)
In recent years, there is aroused interest in expressing complex systems as networks of interacting nodes. Using descriptors from graph theory, it has been possible to classify many diverse systems derived from social and physical sciences alike. In particular, folded
Alexandra Sperschneider et al.
ACS nano, 4(10), 5609-5616 (2010-09-17)
We report on the quasi in situ scanning force microscopy nanotomography which proved to be a key method to effectively obtain a three-dimensional (3D) microdomain structure of a complex ABC triblock morphology. As an example, we studied polybutadiene-block-poly(2-vinyl pyridine)-block-poly(tert-butyl methacrylate)
Mechanochemistry: Demonstrated leverage.
Roman Boulatov
Nature chemistry, 5(2), 84-86 (2013-01-25)
Aleer M Yol et al.
Journal of the American Society for Mass Spectrometry, 24(1), 74-82 (2012-11-30)
[M + Ag](+) ions from cyclic and linear polystyrenes and polybutadienes, formed by matrix-assisted laser desorption ionization (MALDI), give rise to significantly different fragmentation patterns in tandem mass spectrometry (MS(2)) experiments. In both cases, fragmentation starts with homolytic cleavage at
Jiayin Yuan et al.
Macromolecular rapid communications, 32(15), 1157-1162 (2011-06-29)
Commercially available 1,2-PB was transformed into a well-defined reactive intermediate by quantitative bromination. The brominated polymer was used as a polyfunctional macroinitiator for the cationic ring-opening polymerization of 2-ethyl-2-oxazoline to yield a water-soluble brush polymer. Nucleophilic substitution of bromide by
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service