58552
2-Methylpropene
purum, ≥99.5%
Synonym(s):
Isobutylene
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About This Item
Linear Formula:
(CH3)2C=CH2
CAS Number:
Molecular Weight:
56.11
Beilstein:
773645
EC Number:
MDL number:
UNSPSC Code:
12142100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
vapor density
2 (vs air)
vapor pressure
3278 mmHg ( 37.7 °C)
grade
purum
Assay
≥99.5%
autoignition temp.
869 °F
bp
−6.9 °C (lit.)
SMILES string
CC(C)=C
InChI
1S/C4H8/c1-4(2)3/h1H2,2-3H3
InChI key
VQTUBCCKSQIDNK-UHFFFAOYSA-N
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Packaging
Cylinder with net ~3.6 kg
DIN 477 nr.1
Other Notes
Sales restrictions may apply
Recommended products
Z742161 DIN 1 Regulator OR 99112 DIN 1 Valve
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Flam. Gas 1 - Press. Gas Liquefied gas
Storage Class Code
2A - Gases
WGK
nwg
Flash Point(F)
-112.0 °F - closed cup
Flash Point(C)
-80 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Jin-Zhou Zhu et al.
Biomaterials, 33(33), 8204-8212 (2012-08-18)
The presence of polymer coating on a coronary stent is a major mediator of coronary inflammation reaction thereby affects re-endothelialization. Poly(styrene-block-isobutylene-block-styrene) (SIBS) is one of the most attractive alternatives to serve as stent coating, but has shown less than optimal
Yoshihiro Kikkawa et al.
Organic & biomolecular chemistry, 10(40), 8087-8094 (2012-09-12)
A series of isobutenyl compounds possessing various alkyl chain lengths (C(n)-1) with a carbon number of n = 14-21 were synthesized and their two-dimensional (2D) structures were systematically studied using scanning tunnelling microscopy (STM) at a highly oriented pyrolytic graphite
Francesco Frusteri et al.
Bioresource technology, 118, 350-358 (2012-06-19)
Etherification of glycerol (GLY) with isobutylene (IB) to produce biofuels was investigated in liquid phase using spherical silica supported Hyflon® catalysts (SSHC). As reference catalyst, Amberlyst® 15 (A-15) acid ion-exchange resin was used. Experiments were carried out in batch mode
Nicolas Cottenye et al.
Chemical communications (Cambridge, England), 48(20), 2615-2617 (2012-02-02)
The polymer modification of short nucleotide sequences has been achieved for future use as self-assembled biologically active structures with sizes in the nanometre range. Co-assembly of the resulting DNA-based amphiphilic block copolymers with native proteins demonstrates the self-assembly of biological-like
Markus Burkhardt et al.
Langmuir : the ACS journal of surfaces and colloids, 24(5), 1769-1777 (2008-01-30)
We report on interpolyelectrolyte complexes (IPECs) formed by micelles of ionic amphiphilic diblock copolymers with polyisobutylene (PIB) and poly(sodium methacrylate) (PMANa) blocks interacting with quaternized poly(4-vinylpyridine) (P4VPQ). The interpolyelectrolyte complexation was followed by turbidimetry and small angle neutron scattering (SANS).
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