1471-16-5

Basic information

• Product Name: 1,4-bis(allyloxy)butane
• Synonyms: 1,4-bis(allyloxy)butane;1,4-Bis(2-propenyloxy)butane;1,4-Butanediylbis(allyl ether)
• CAS NO: 1471-16-5
• Molecular Formula: C₁₀H₁₈O₂
• Molecular Weight: 170.24872
• EINECS: 216-007-9
• Mol File: 1471-16-5.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 211.5°Cat760mmHg
• Flash Point: 69.5°C
• Appearance: /
• Density: 0.866g/cm³
• Vapor Pressure: 0.264mmHg at 25°C
• Refractive Index: 1.435
• CAS DataBase Reference: 1,4-bis(allyloxy)butane(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-bis(allyloxy)butane(1471-16-5)
• EPA Substance Registry System: 1,4-bis(allyloxy)butane(1471-16-5)

Safety Data

• Hazardous Substances Data: 1471-16-5(Hazardous Substances Data)

Usage

General Description

1,4-bis(allyloxy)butane, also known as Diallyl adipate, is a chemical compound with the molecular formula C14H24O4. It is a colorless to pale yellow liquid that is commonly used as a crosslinking agent in the production of polymers and resins. 1,4-bis(allyloxy)butane is known for its ability to increase the strength and flexibility of various polymers, making it useful in a wide range of industrial applications. It is also used as a plasticizer in the production of vinyl and other plastics. Additionally, 1,4-bis(allyloxy)butane is considered to be relatively safe for use in these applications, as it has low toxicity and is not known to be a carcinogen.

InChI:InChI=1/C10H18O2/c1-3-7-11-9-5-6-10-12-8-4-2/h3-4H,1-2,5-10H2

Upstream product

• 110-63-4 Butane-1,4-diol 
• 107-18-6 allyl alcohol 
• 107-05-1 3-chloroprop-1-ene 
• 110-52-1 1,4-dibromo-butane 

Downstream Products

• 110-63-4 Butane-1,4-diol 

Relevant articles and documents

Synthesis, characterization, thermal and computational studies of novel tetra–azido compounds as energetic plasticizers

In this paper, four azido compounds have been synthesized and characterized as new energetic plasticizers. Nuclear magnetic resonance (NMR) and infrared (IR) spectroscopy, elemental analysis, differential scanning calorimetry (DSC), thermogravimetric analysis (TGA) and differential thermal analysis (DTA) have been used to identify and determine the properties of the synthesized plasticizers. The plasticization effect of plasticizers on glycidyl azide polymer (GAP) has been investigated by viscosity measurements and thermal analysis of the prepolymer–plasticizer mixtures and plasticized binders. The plasticized mixtures were cured by a diisocyanate curing agent and the glass transition temperature and decomposition temperature of the cured polyurethane binders were measured. Thermal analysis of the prepolymer–plasticizer and cured polymer mixtures showed that the synthesized plasticizers are completely compatible with the GAP binder and have a very good plasticizing effect. Furthermore, equilibrium geometry and heats of formation of each of the plasticizer molecules were obtained using the thermochemical T1 recipe, which is available in wave function Spartan software. Comparing empirical heats of combustion and calculated heats of combustion by using the heats of formation showed that the suggested optimum molecular structure by the T1 recipe has a high similarity to the real molecular structure of these molecules.

The effectiveness of ruthenium(II) complexes and ruthenium trichloride as pre-catalysts in solvent-free isomerization of model alkyl allyl ether

The isomerization of readily available allyl ethers catalyzed by soluble ruthenium complexes is an extremely versatile methodology for synthesis of O-1-propenyl systems-attractive monomers in cationic UV-radiation curing technology. From the process development perspective, the effectiveness of selected simple ruthenium catalyst precursors, mainly [RuClH(CO)(PPh3)3], [RuCl2(PPh3)3] and RuCl3·xH2O in the solvent-free isomerization of 1,4-bisallyloxybutane has been examined. The relationship between basic reaction parameters such as the reaction temperature, the amount of catalyst precursor, the promoters of non-hydride complexes (bases or alcohols), the ambient gas atmosphere and the reaction time allowing to achieve quantitative conversion of the model bisallyl ether to its 1-propenyl derivatives (τ100%) has been presented. Particular attention has been paid to the use of lower loadings of [Ru] complex required for the completion of the reaction within the reasonable times. For the first time a detailed study on the effect of the presence and amount of allyl hydroperoxides on the course of isomerization has been done.

Isomerization of allyl ethers of diols and triols catalyzed by ruthenium complexes

-