Dicyclohexyl Phthalate Dicyclohexyl Phthalate
Structural formula
| Business number | 01UV |
|---|---|
| Molecular formula | C20H26O4 |
| Molecular weight | 330.42 |
| label |
1,2-Dicyclohexylphthalate, Dicyclohexyl phthalate, DCHP, C6H4-1,2-(CO2C6H11)2, Dicyclohexyl benzene-1,2-dicarboxylate, Ergoplast FDC, DCHP, Plasticizer |
Numbering system
CAS number:84-61-7
MDL number:MFCD00003849
EINECS number:201-545-9
RTECS number:TI0889000
BRN number:201-545-9
PubChem number:24862790
Physical property data
1. Properties: white crystalline powder
2. Relative density (25/25℃): 1.20
3. Melting point (℃): 65
4. Boiling point (℃): 220~228
5. Flash point (℃): 207
6. Ignition point (℃): 240
7 . Vapor pressure (150℃): 12Pa
8. Solubility: Hardly soluble in water, slightly soluble in ethylene glycol and some amines, soluble in acetone, methyl ethyl ketone, cyclohexanone, ether, Carbon tetrachloride, toluene and other organic solvents. Has good compatibility with many resins.
Toxicological data
1. Acute toxicity:
Mouse caliber LD50: 30mg/kg
2. Other multiple dose toxicity:
Rat caliber TDL0: 10500 mg/kg/7D-I
Ecological data
None yet
Molecular structure data
1. Molar refractive index: 91.16
2. Molar volume (cm3/mol): 288.6
3. Isotonic specific volume (90.2K): 750.7
4. Surface tension (dyne/cm): 45.7
5. Polarizability (10-24cm3): 36.13
Compute chemical data
1. Reference value for hydrophobic parameter calculation (XlogP): None
2. Number of hydrogen bond donors: 0
3. Number of hydrogen bond acceptors: 4
4. Number of rotatable chemical bonds: 6
5. Number of tautomers: none
6. Topological molecule polar surface area 52.6
7. Number of heavy atoms: 24
8. Surface charge: 0
9. Complexity: 381
10. Number of isotope atoms: 0
11. Determine the number of atomic stereocenters: 0
12. Uncertain number of atomic stereocenters: 0
13. Determine the number of chemical bond stereocenters: 0
14. Number of uncertain chemical bond stereocenters: 0
15. Number of covalent bond units: 1
Properties and stability
1%Aqueous solutionpH is 3.13. It is relatively stable in pH2-4 aqueous solution, pH5.5The above are unstable to heating and will decompose when exposed to ultraviolet rays. It is stable in the air in a dry state, absorbs moisture quickly and decomposes slowly when exposed to the air.
Storage method
Stored in a cool, ventilated warehouse, away from fire sources.
Synthesis method
1. Use phthalic anhydride and cyclohexanol as raw materials, the feeding ratio is phthalic anhydride: cyclohexanol = 1:2.4, and use sulfuric acid (0.2% of the total feeding amount) as the catalyst to carry out esterification reaction. The reaction pressure is 0.08MPa, the reaction temperature is 120°C, and the reaction time is 2 to 3 hours. The crude ester liquid is first neutralized with alkali, then washed with water, and then the cyclohexanol is removed by direct steam distillation. The product is obtained after drying, crushing and sieving.
2.Add cyclohexanol into the reaction kettle, add sulfuric acid as a catalyst while stirring, then add phthalic anhydride to dissolve, continue to heat up, and reduce pressure continuously. Remove the by-products to obtain the product
3.The esterification reaction is carried out in a laboratory equipped with a thermometer, reflux condenser, stirrer, and air guide tube In the reaction kettle, add cyclohexanol, solvent A (the dosage is 10% to 20% of the mass of phthalic anhydride), and phthalic anhydride quantitatively, heat to reflux, and add the catalyst (1.5% to 2.0% of the mass of phthalic anhydride) within the specified time. Maintain the reflux temperature and continue the reaction for 13 to 15 hours until the water content reaches the expected value. Take a sample to measure the acid value and calculate the conversion rate. The alkyd-acid feeding ratio is (2.5~2.7):1 (molar ratio).
4.Neutralization, water washing, and distillation. Cool the esterification liquid to the specified temperature, add soda ash solution, neutralize, and wash with water. Thereafter, the mixture is heated and distilled to recover solvent A and excess cyclohexanol.
5.Decolorize and refine the crude ester after distillation, add additive B (the amount added is 5% of the ester amount ~15%), control the temperature between 70 and 120°C, carry out decolorization, purification, and remove a small amount of impurities to obtain the refined ester. Finally, the obtained refined ester is cooled, solidified, and crushed to obtain the finished product.
Purpose
1. This product is a phthalate plasticizer. This type of plasticizer has many varieties and large output, accounting for about 80% of the total plasticizer output. It has relatively comprehensive properties and is generally used as the main plasticizer. Among phthalates, dioctyl phthalate (DOP) is the most widely used, accounting for approximately 45% of the total plasticizers in my country. Dicyclohexyl phthalate can be used as the main plasticizer for polyvinyl chloride, acrylic resin, polystyrene, nitrocellulose and other resins. It has a moisture-proof effect. When used together with other plasticizers, it can make the product shrink and dense, preventing Water vapor transmission and plasticizer evaporation. Plastic products containing this product have smooth surfaces and good hand feel. The dosage of this product generally accounts for 10-20% of the total plasticizer dosage. The dosage should not be too large, otherwise the hardness of the product will increase. This product can improve the fluidity of resin during thermal processing. In synthetic resin adhesives, this product can improve the adhesion, oil resistance and durability. In addition, this product is also used in nitrocellulose and some natural resins to make moisture-proof coatings. This product has low toxicity. After rats were directly orally exposed to olive oil containing 25% of this product, there were no deaths within 24 hours. The LD50 within 7 days was 30ml/kg. This product was mixed into the feed at a dose of 10 mg/kg and fed to rats for four generations for 8 months. No abnormalities were found in the growth, reproduction, and lactation of the experimental animals, and it was not carcinogenic.
2. It can be used as the main plasticizer for polyvinyl chloride, acrylic resin, polystyrene, nitrocellulose and other resins. It has good water resistance and is a moisture-proof plasticizer. It can also be used in moisture-proof cellophane coatings and moisture-proof coatings for paper. Among synthetic resin adhesives, this product can improve its adhesion, oil resistance and durability. The dosage of this product generally accounts for 10% to 20% of the total plasticizer dosage. The United States, Japan, Germany, Italy and other countries allow packaging materials that come into contact with food, such as food packaging bags, fresh-keeping bags, plastic wrap, etc.
