Structural formula

Business number	01FC
Molecular formula	C8H4Cl6
Molecular weight	312.84
label	1,4-Bis(trichloromethyl)benzene, α,α,α,α’,α’,α’-hexachloro-p-xylene, For hexachlorobenzyl, Hexachloroparaxylene, 1,4-bistrichlorotoluene, Α,Α,Α,Α’,Α’,Α’-hexachloro-p-xylene, antischistosomiasis drugs

• Numbering system
• Physical property data
• Toxicological data
• Ecological data
• Molecular structure data
• Computing chemical data
• More
  • Properties and Stability
  • Storage method
  • Synthesis method
  • Purpose

Numbering system

CAS number:68-36-0

MDL number:MFCD00000791

EINECS number:200-686-3

RTECS number:ZE4655000

BRN number:None

PubChem ID:None

Physical property data

1. Properties: White needle-like crystals or crystalline powder, with a special odor and tasteless. It will slowly decompose when exposed to light and alkali and become acidic

2. Density (g/mL, 25/4℃): Uncertain

3. Relative vapor density (g/mL, Air=1): Uncertain

4. Melting point (ºC): 106-110

5. Boiling point (ºC, normal pressure): 312

6 . Boiling point (ºC, 5.2kPa): Uncertain

7. Refractive index: Uncertain

8. Flash point (ºC): Uncertain

9 . Specific rotation (º): Uncertain

10. Autoignition point or ignition temperature (ºC): Uncertain

11. Vapor pressure (kPa, 25ºC): Uncertain

12. Saturated vapor pressure (kPa, 60ºC): Uncertain

13. Heat of combustion (KJ/mol): Uncertain

14. Critical temperature (ºC): Uncertain

15. Critical pressure (KPa): Uncertain

16. Log value of oil-water (octanol/water) partition coefficient: Uncertain

17. Explosion upper limit (%, V/V): Uncertain

18. Explosion lower limit (%, V/V): Uncertain

19. Solubility : Insoluble in water, easily soluble in ethanol, xylene, petroleum ether and vegetable oil, etc.

Toxicological data

Acute toxicity: Rat oral LD50: 3200 mg/kg; Breeding: Rat oral TDLo: 2330 mg/kgSEX/DURATION: male 26 week(s) pre-mating; Rat oral TDLo: 2330 mg/kgSEX/ DURATION: female 26 weeks(s) pre-mating;

Ecological data

None

Molecular structure data

1. Molar refractive index: 64.32

2. Molar volume (cm³/mol): 192.0

3.   Isotonic volume (90.2K): 495.2

4. Surface tension (dyne/cm): 44.2

5. Polarizability (10-24cm3): 25.50

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 molecule polar surface area 0

7. Number of heavy atoms: 14

8. Surface charge: 0

9. Complexity: 161

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

None

Storage method

Store in an airtight container away from light.

Synthesis method

Using mixed xylene as raw material, it is first sulfonated with 98% sulfuric acid to generate m-xylene sulfonate. The oil layer containing o- and p-xylene is separated from the sulfonation reaction product, washed with water, dried, and o- and p-xylene is distilled under reduced pressure. The by-product m-xylene can be obtained by hydrolysis of m-xylene sulfonate. 1,4-bis(trichloromethyl)benzene is obtained by chlorination of o- and p-xylene: put o- and p-xylene into the reaction pot, and then add benzoyl peroxide and triethanolamine. After heating to 70°C, introduce chlorine gas under light irradiation, react at 70-80°C for 6 hours, and then raise the temperature to 100-120°C to continue the reaction until the relative density of the reaction solution reaches 1.560-1.580 (65°C), which is the end point of the reaction. Stop passing chlorine and remove residual chlorine under reduced pressure. Cool to 5°C, filter, wash to obtain crude product, recrystallize, and decolorize with activated carbon to obtain finished product.

Purpose

Anti-schistosomiasis drugs. It has certain effects on liver fluke disease, amoebiasis, malaria and intestinal nematodes. However, adverse reactions to the nervous system are more common, and delayed reactions last longer.

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