15199-41-4

Basic information

• Product Name: 1,2-CYCLODODECANEDIOL
• Synonyms: 1,2-CYCLODODECANEDIOL;1,2-Cyclododecanediol (cis- and trans- mixture);Cyclododecanediol;cyclododecane-1,2-diol;cis-/trans-mixture;1,2-CYCLODODECANEDIOL (CIS+ TRANS);EINECS 239-256-5;1,2-CYCLODODECANEDIOL (CIS- AND TRANS- MIXTURE) 87+%
• CAS NO: 15199-41-4
• Molecular Formula: C₁₂H₂₄O₂
• Molecular Weight: 200.32
• EINECS: 239-256-5
• Mol File: 15199-41-4.mol
• Article Data: 5

Chemical Properties

• Melting Point: 121.0 to 125.0 °C
• Boiling Point: 339.7 °C at 760 mmHg
• Flash Point: 158.2 °C
• Appearance: /
• Density: 0.968 g/cm³
• Vapor Pressure: 6.04E-06mmHg at 25°C
• Refractive Index: 1.477
• CAS DataBase Reference: 1,2-CYCLODODECANEDIOL(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-CYCLODODECANEDIOL(15199-41-4)
• EPA Substance Registry System: 1,2-CYCLODODECANEDIOL(15199-41-4)

Safety Data

• Hazardous Substances Data: 15199-41-4(Hazardous Substances Data)

Usage

General Description

1,2-Cyclododecanediol, also known as 1,2-Dodecanediol, is a colorless, viscous liquid chemical compound. It is used in various applications such as in the production of adhesives, coatings, and plastics. It is also used as an intermediate in the synthesis of fragrances and pharmaceuticals. 1,2-Cyclododecanediol is known for its ability to act as a crosslinking agent in the production of polyurethane and other polymers, making it a versatile and important chemical in the manufacturing industry. Additionally, it is considered to be relatively safe for use and handling, with low toxicity and low hazard potential.

InChI:InChI=1/C12H24O2/c13-11-9-7-5-3-1-2-4-6-8-10-12(11)14/h11-14H,1-10H2

Upstream product

• 1486-75-5 (E)-Cyclododecen 
• 50381-48-1 trioxo(N-tert-butylimido)osmium(VIII) 
• 1129-89-1 cis-cyclododecene 
• 1501-82-2 cyclododecene 
• 64-18-6 formic acid 
• 7722-84-1 dihydrogen peroxide 
• 38279-34-4 dodecanedial 
• 294-62-2 cyclododecane 

Downstream Products

• 38279-34-4 dodecanedial 
• 693-23-2 1,12-dodecanedioic acid 
• 24413-57-8 1,2-bis-[3-(3,5-Di-t-butyl-4-hydroxyphenyl)propionyloxy]cyclododecane 

Relevant articles and documents

Oxidation of alkenes by oxodiperoxomolybdenum: Trialkyl(aryl)phosphine oxide complexes

Catalytic amounts of short-chain (2-4 carbons) trialkylphosphine oxide ligands and MoO5 have been shown to efficiently convert di- and higher substituted alkenes to the corresponding epoxides using a biphasic system with either 30% hydrogen peroxide or 70% TBHP acting as the stoichiometric oxidant. Georg Thieme Verlag Stuttgart.

Dendritic phosphonates and the in situ assembly of polyperoxophosphotungstates: Synthesis and catalytic epoxidation of alkenes with hydrogen peroxide

First and second-generation rigid dendrimers based on polyphenylated tetrahedral adamantane cores with four or sixteen peripheral phosphonate moieties, PD1 and PD2, respectively, were synthesized and characterized. Further reaction of the dendritic phosphonates with tungstic acid in the presence of hydrogen peroxide led to the stepwise in situ formation of mono- and dinuclear phosphoperoxotungstates. These assemblies were effective catalysts for the epoxidation of alkenes in an aqueous acetonitrile solvent.

Permanganate Ion Oxidations. 19. Hexadecyltrimethylammonium Permanganate Oxidation of Cycloalkenes

The kinetics of hexadecyltrimethylammonium permanganate (cetyltrimethylammonium permanganate, CTAP) oxidation of cycloalkenes in dichloromethane have been studied.The relative rates of oxidation versus 13C NMR chemical shifts, vertical ionization potentials, and strain energies are discussed.A comparison of the relative rate of permanganate ion oxidation with the relative rates of addition of other reagents to carbon-carbon double bonds suggests that it may act as a 1,3-dipole.