Epoxy curing agent Knowledge 1,5-Cycloctadiene 1,5-Cyclooctadiene

1,5-Cycloctadiene 1,5-Cyclooctadiene

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1,5-cyclooctadiene structural formula

Structural formula

Business number 034A
Molecular formula C8H12
Molecular weight 108.18
label

cis,cis-1,5-cyclooctadiene,

1,5-cyclooctadiene,

Cis,cis-1,5-cyclooctadiene,

1,5-Cyclooctadiene,

hydrocarbon solvents,

Alicyclic compounds

Numbering system

CAS number:111-78-4

MDL number:MFCD00001752

EINECS number:203-907-1

RTECS number:GX9620000

BRN number:2036542

PubChem number:24854773

Physical property data

1. Properties: colorless liquid

2. Boiling point (ºC, normal pressure): 150.9

3. Melting point (ºC): -70

4. Relative density (g/mL, 20/4ºC): 0.881

5. Refractive index (20ºC): 1.4933

6. Viscosity (mPa·s, 20ºC): 1.38

7. Viscosity (mPa·s, 50ºC): 0.87

8. Viscosity (mPa·s, 100ºC): 0.51

9. Specific heat capacity ( KJ/(kg·K), 50ºC): 2.010

10. Specific heat capacity (KJ/(kg·K), 100ºC): 2.180

11. Specific heat capacity (KJ/(kg ·K), 150ºC): 2.390

12. Thermal conductivity (W/(m·K), 30ºC): 0.1289

13. Heat of evaporation (KJ/mol, 101.3 kPa): 38.940

14. Flash point (ºC): 35

15. Fire point (ºC): 270

16. Vapor pressure (kPa, 20ºC ): 0.67

17. Solubility: Insoluble in water, insoluble in carbon tetrachloride.

Toxicological data

It has a strong irritating effect on mucous membranes and skin, causing skin allergies. There is no permanent harm to humans.

Ecological data

This substance is harmful to the environment, and special attention should be paid to atmospheric pollution.

Molecular structure data

1. Molar refractive index: 36.10

2. Molar volume (cm3/mol): 128.5

3. Isotonic specific volume (90.2K): 303.0

4. Surface tension (dyne/cm): 30.9

5. Polarizability (10-24cm3): 14.31

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: 0

4. Number of rotatable chemical bonds: 0

5. Number of tautomers: None

6. Topological molecular polaritySurface area 0

7. Number of heavy atoms: 8

8. Surface charge: 0

9. Complexity: 72.6

10 .The number of isotope atoms: 0

11. The number of determined atomic stereocenters: 0

12. The number of uncertain atomic stereocenters: 0

13. Determined number of chemical bond stereocenters: 2

14. Uncertain number of chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

  1. No contact with strong oxidizing agents. Strictly avoid contact with skin and eyes during use, storage and transportation.
  • Hydrogenation produces cyclooctane or cyclooctene, and epoxidation reaction can produce cyclosuberic acid, which is an important raw material for unsaturated polyesters and alkyd resins. Diene addition reaction can occur, and halogen addition gives tetrachlorocyclooctane, which is an important flame retardant.
  • 2.This product has low toxicity, but can irritate the skin, cause allergies, dermatitis, and inflammation of the eyes and eyelids. Operators during production should wear protective equipment. Production equipment should be sealed and the workshop should be well ventilated.
     
  • Storage method

    Stored in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 30. should be kept away from oxidizer, do not store together. It should not be stored for a long time to avoid deterioration. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency release equipment and suitable containment materials.

    Should be stored in stainless steel bottles or plastic barrels in a cool, ventilated, dry warehouse, away from fire and heat sources. Store and transport according to general chemical regulations.

    Synthesis method

    Produced by the dimerization and cyclization of butadiene.

    Purpose

    It can also be used as an organic synthesis intermediate to prepare suberic acid, octenedioic acid, tetrachlorocyclooctane, etc. It can also be used as the third monomer of ethylene-propylene rubber.

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