1,2-Dodecylene Oxide

Product Information

Molecular Formula:
C12H24O
Molecular Weight:
184.32
Description
1,2-epoxydodecane is a clear colorless liquid.
Synonyms
1-Dodecene Epoxide||||1,2-Dodecylene Oxide
IUPAC Name
2-decyloxirane
Canonical SMILES
CCCCCCCCCCC1CO1
InChI
InChI=1S/C12H24O/c1-2-3-4-5-6-7-8-9-10-12-11-13-12/h12H,2-11H2,1H3
InChI Key
MPGABYXKKCLIRW-UHFFFAOYSA-N
Boiling Point
85 ℃/1 mmHg
Flash Point
105 ℃
Purity
>95.0%(GC)
Density
0.844 g/mL at 25 ℃ (lit.)
Solubility
less than 1 mg/mL at 73 °F
Appearance
Colorless to Almost colorless clear liquid
Application
Used as a secondary heat stabilizer for polymers; No known commercial production in the US.
Storage
2-8℃
Refractive Index
n20/D 1.436 (lit.)
Vapor Pressure
6.25 mmHg at 77 °F

Safety Information

Hazards
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
Precautionary Statement
P264:
Wash thoroughly after handling.
P280:
Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352:
IF ON SKIN:
Wash with plenty of soap and water.
P332+P313:
If skin irritation occurs:
Get medical advice/attention.
P337+P313:
If eye irritation persists:
Get medical advice/attention.
P362+P364:
Take off contaminated clothing. [As modified by IV ATP].
And wash it before reuse. [Added by IV ATP].

Computed Properties

XLogP3
5.2
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
9
Exact Mass
184.182715385 g/mol
Monoisotopic Mass
184.182715385 g/mol
Topological Polar Surface Area
12.5Ų
Heavy Atom Count
13
Formal Charge
0
Complexity
112
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
1
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-114105799-A Amino lipid and preparation method and application thereof 2022-01-25
CN-113956486-A Long-chain branched polylactic acid-based copolymer and preparation method thereof 2021-11-11
CN-113773172-A Method for synthesizing lichen moth sex pheromone and diastereomer thereof 2021-09-14
CN-113907952-A Non-stick dressing and preparation method thereof 2021-08-31
CN-113461504-A Method for preparing macrocyclic alkanone from epoxide 2021-08-13
CN-113403313-A sgRNA, plasmid and nano-composite for specifically recognizing human PLK1 locus and application 2021-06-23
CN-113548974-A Polyaspartic acid ester and preparation method and application thereof 2021-06-22
CN-113024825-A Modified polyamide complex silver and preparation method thereof 2021-02-26
CN-113026367-A Medical silver-carrying gauze and preparation method thereof 2021-02-26
CN-112438257-A Surfactant and application thereof in oil-based pesticide formulation 2020-12-08

Literatures

PMID Publication Date Title Journal
22570637 2012-01-01 YY1 regulates melanocyte development and function by cooperating with MITF PLoS genetics
21563767 2011-06-06 Aluminum nanoparticles capped by polymerization of alkyl-substituted epoxides: ratio-dependent stability and particle size Inorganic chemistry
20178368 2010-04-05 Organically modified zirconium phosphate by reaction with 1,2-epoxydodecane as host material for polymer intercalation: synthesis and physicochemical characterization Inorganic chemistry
19583230 2009-08-18 Capping and passivation of aluminum nanoparticles using alkyl-substituted epoxides Langmuir : the ACS journal of surfaces and colloids
19167513 2009-03-17 Intralaboratory and interlaboratory evaluation of the EpiDerm 3D human reconstructed skin micronucleus (RSMN) assay Mutation research
18337067 2008-07-15 Nucleotides and nucleolipids derivatives interaction effects during multi-lamellar vesicles formation Colloids and surfaces. B, Biointerfaces
17902712 2007-10-23 Air and water free solid-phase synthesis of thiol stabilized au nanoparticles with anchored, recyclable dendrimer templates Langmuir : the ACS journal of surfaces and colloids
16200537 2005-11-01 Improved catalytic activity of homochiral dimeric cobalt-salen complex in hydrolytic kinetic resolution of terminal racemic epoxides Chirality
12154317 2002-08-01 (1S,3R,8S,9S,10R)-2,2-Dichloro-9,10-epoxy-3,7,7,10-tetramethyltricyclo[6.4.0.0(1,3)]dodecane and (1S,3R,8S,10R)-2,2-dichloro-3,7,7,10-tetramethyltricyclo[6.4.0.0(1,3)]dodecan-9-one Acta crystallographica. Section C, Crystal structure communications
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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