1,9-Decadiene

Product Information

Molecular Formula:
C10H18
Molecular Weight:
138.25
Description
Applications: 1,​9-​Decadiene is used in acyclic diene metathesis copolymerization (ADMET) along with 1, 5-hexadiene to form polybutadiene -polyoctenamer copolymers.Dangerous Goods Info: Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package.
Synonyms
deca-1,9-diene
IUPAC Name
deca-1,9-diene
Canonical SMILES
C=CCCCCCCC=C
InChI
InChI=1S/C10H18/c1-3-5-7-9-10-8-6-4-2/h3-4H,1-2,5-10H2
InChI Key
NLDGJRWPPOSWLC-UHFFFAOYSA-N
Boiling Point
169 °C
Purity
95 %
Density
0.752 g/cm3
Appearance
Clear colorless to slightly yellow liquid
Storage
Flammables area
Refractive Index
n20/D 1.432 (lit.)
LogP
3.69900

Safety Information

Hazards
H226-H315-H319-H335-H400
Precautionary Statement
P210, P233, P240, P241, P242, P243, P261, P264, P271, P273, P280, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P370+P378, P391, P403+P233, P403+P235, P405, and P501
Signal Word
Warning

Computed Properties

XLogP3
5.1
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
7
Exact Mass
138.140850574 g/mol
Monoisotopic Mass
138.140850574 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
10
Formal Charge
0
Complexity
70
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
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-114163552-A Modified silica gel and preparation method and application thereof, and supported catalyst and preparation method and application thereof 2022-01-05
CN-114042055-A Agomelatine transdermal patch as well as preparation method and application thereof 2021-12-29
CN-113896998-A Preparation method of polyolefin thermoplastic elastomer based on dynamic crosslinking modification 2021-10-12
CN-114014970-A Preparation method of carbomer, carbomer oral gel and preparation method thereof 2021-09-30
CN-113637101-A Catalyst for alpha-olefin polymerization, preparation method and application 2021-09-02
CN-113444229-A Preparation method of fluorine-containing alternating polymer 2021-06-28
CN-113402641-A Metallocene catalyst, preparation method and application 2021-06-02
CN-113116814-A Vanillan transdermal solution and preparation method and application thereof 2021-04-01
JP-2021075457-A Surface-modified nanodiamond 2021-02-02
CN-114181530-A Bioelectrode composition, bioelectrode, method for producing bioelectrode, and silicon material particle 2020-09-15

Literatures

PMID Publication Date Title Journal
21384004 2011-04-14 Synthesis of [3]ferrocenophane-bridged Cp-amido zirconium complexes and ansa-zirconocene complexes and their use in catalytic polymerisation reactions Dalton transactions (Cambridge, England : 2003)
20519856 2010-06-01 [Search for TNF-alpha sensitivity degradation principles from medicinal foods-hepatoprotective amide constituents from Thai natural medicine Piper chaba] Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan
19760711 2009-10-19 ESIMS studies and calculations on alkali-metal adduct ions of ruthenium olefin metathesis catalysts and their catalytic activity in metathesis reactions Chemistry (Weinheim an der Bergstrasse, Germany)
19775895 2009-10-15 Hepatoprotective amide constituents from the fruit of Piper chaba: Structural requirements, mode of action, and new amides Bioorganic & medicinal chemistry
19618951 2009-08-12 Ethenolysis reactions catalyzed by imido alkylidene monoaryloxide monopyrrolide (MAP) complexes of molybdenum Journal of the American Chemical Society
18355031 2008-05-01 Development of structure-lipid bilayer permeability relationships for peptide-like small organic molecules Molecular pharmaceutics
18289853 2008-03-15 Protective effects of amide constituents from the fruit of Piper chaba on D-galactosamine/TNF-alpha-induced cell death in mouse hepatocytes Bioorganic & medicinal chemistry letters
17879989 2008-01-01 Liposome transport of hydrophobic drugs: gel phase lipid bilayer permeability and partitioning of the lactone form of a hydrophobic camptothecin, DB-67 Journal of pharmaceutical sciences
16504068 2006-02-22 Common features and interesting differences in transcriptional responses to secretion stress in the fungi Trichoderma reesei and Saccharomyces cerevisiae BMC genomics
17722279 2006-01-01 Silicon nanoparticles: applications in cell biology and medicine International journal of nanomedicine
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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