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Details

Stereochemistry ACHIRAL
Molecular Formula C6H12
Molecular Weight 84.1595
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-METHYL-1-PENTENE

SMILES

CC(C)CC=C

InChI

InChIKey=WSSSPWUEQFSQQG-UHFFFAOYSA-N
InChI=1S/C6H12/c1-4-5-6(2)3/h4,6H,1,5H2,2-3H3

HIDE SMILES / InChI

Molecular Formula C6H12
Molecular Weight 84.1595
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Reduced thrombocyte adhesion to endothelialized poly 4-methyl-1-pentene gas exchange membranes—a first step toward bioartificial lung development.
2010-10
Decomposition and isomerization of 5-methylhex-1-yl radical.
2010-08-05
Temperature-dependent ozonolysis kinetics of selected alkenes in the gas phase: an experimental and structure-activity relationship (SAR) study.
2010-03-28
Elimination of sevoflurane is reduced in plasma-tight compared to conventional membrane oxygenators.
2008-02
Mechanism of activation of a hafnium pyridyl-amide olefin polymerization catalyst: ligand modification by monomer.
2007-06-27
Diastereomerically-specific zirconium complexes of chiral salan ligands: isospecific polymerization of 1-hexene and 4-methyl-1-pentene and cyclopolymerization of 1,5-hexadiene.
2006-10-11
Hafnocene catalysts for selective propylene oligomerization: efficient synthesis of 4-methyl-1-pentene by beta-methyl transfer.
2006-10-04
Dispersion of single-walled carbon nanotubes in a non-polar polymer, poly(4-methyl-1-pentene).
2006-08
Hugoniot data of plastic foams obtained from laser-driven shocks.
2006-04
Structure determination of oligomeric alkannin and shikonin derivatives.
2005-09
Unprecedented syndioselectivity and syndiotactic polyolefin melting temperature: polypropylene and poly(4-methyl-1-pentene) from a highly active, sterically expanded eta1-fluorenyl-eta1-amido zirconium complex.
2005-07-20
Antihistamine effects of triprolidine from the transdermal administration of the TPX matrix in rats.
2005-01
A sterically expanded "constrained geometry catalyst" for highly active olefin polymerization and copolymerization: an unyielding comonomer effect.
2004-12-29
FTIR and FT Raman spectra and analysis of poly(4-methyl-1-pentene).
2004-01
Transdermal delivery of triprolidine using TPX polymer membrane.
2002-03-20
Enhanced bioavailability of triprolidine from the transdermal TPX matrix system in rabbits.
2002-03-02
Application of TPX polymer membranes for the controlled release of triprolidine.
2002-01-31
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:28:09 GMT 2025
Edited
by admin
on Mon Mar 31 19:28:09 GMT 2025
Record UNII
X10HRJ2Y7W
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-METHYL-1-PENTENE
Systematic Name English
NSC-15091
Preferred Name English
1-PENTENE, 4-METHYL-
Systematic Name English
ISOBUTYLETHENE
Systematic Name English
Code System Code Type Description
CAS
691-37-2
Created by admin on Mon Mar 31 19:28:09 GMT 2025 , Edited by admin on Mon Mar 31 19:28:09 GMT 2025
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PUBCHEM
12724
Created by admin on Mon Mar 31 19:28:09 GMT 2025 , Edited by admin on Mon Mar 31 19:28:09 GMT 2025
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NSC
15091
Created by admin on Mon Mar 31 19:28:09 GMT 2025 , Edited by admin on Mon Mar 31 19:28:09 GMT 2025
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WIKIPEDIA
4-METHYL-1-PENTENE
Created by admin on Mon Mar 31 19:28:09 GMT 2025 , Edited by admin on Mon Mar 31 19:28:09 GMT 2025
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ECHA (EC/EINECS)
211-720-1
Created by admin on Mon Mar 31 19:28:09 GMT 2025 , Edited by admin on Mon Mar 31 19:28:09 GMT 2025
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FDA UNII
X10HRJ2Y7W
Created by admin on Mon Mar 31 19:28:09 GMT 2025 , Edited by admin on Mon Mar 31 19:28:09 GMT 2025
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EPA CompTox
DTXSID3061001
Created by admin on Mon Mar 31 19:28:09 GMT 2025 , Edited by admin on Mon Mar 31 19:28:09 GMT 2025
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