466867
Polybutadiene, predominantly 1,2-addition
approx. 90% 1,2-vinyl
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About This Item
Linear Formula:
[CH2CH(CH=CH2)]n
CAS Number:
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12162002
MDL number:
Quality Segment
feature
hydrophobic
refractive index
n
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
10 - Combustible liquids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
PPE (personal protective equipment)
Eyeshields, Gloves, type N95 (US)
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