Polyether_Polyether Polyol News 2,4-Dichlorophenoxybutyric acid

2,4-Dichlorophenoxybutyric acid

2,4-Dichlorophenoxybutyric acid structural formula

Structural formula

Business number 0288
Molecular formula C10H10Cl2O3
Molecular weight 249.09
label

2,4-D butyric acid,

2,4-D butyric acid,

4-(2,4-Dichlorophenoxy)butyric acid,

Butyrac,Legumex,Embutox,

herbicide

Numbering system

CAS number:94-82-6

MDL number:MFCD00002819

EINECS number:202-366-9

RTECS number:ES9100000

BRN number:1976809

PubChem number:24855841

Physical property data

1. Properties: white crystal.

2. Density (g/mL, 20℃): 1.2428

3. Relative vapor density (g/mL, air=1): Undetermined

4. Melting point (ºC): 117~119

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

6. Boiling point (ºC, KPa): Undetermined

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7. Refractive index: Undetermined

8. Flash point (ºC): Undetermined

9. Specific rotation (º): Undetermined

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

11. Vapor pressure (mmHg,ºC): Undetermined

12. Saturated vapor pressure ( kPa, ºC): Undetermined

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

14. Critical temperature (ºC): Undetermined

15. Critical pressure (KPa): Undetermined

16. Log value of oil-water (octanol/water) distribution coefficient: Undetermined

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

18. Lower explosion limit (%, V/V): Undetermined

19. Solubility: Hardly soluble in water, easily soluble in most organic solvents.

Toxicological data

1. Acute toxicity: rat oral LD50: 700mg/kg; rat skin contact LD50: 800mg/kg; mouse oral LDLo: 750mg/kg; rabbit skin contact LD50: >10mg/kg;

2. Other multiple dose toxicity: Rat oral TDLo: 18928mg/kg/13W-I; Rat oral TDLo: 4368mg/kg/60W-I; Rat oral TDLo: 5mg/ kg/10D-I;

3. Reproductive toxicity

Rat oral TDLo: 17mg/kg (female rats are pregnant for 1-7 days); Rat oral TDLo: 416mg /kg (5 days after conception in female rats); Oral TDLo in rats: 416 mg/kg (9 days after conception in female rats);

4. Mutagenicity

E. coli DNA repair :5mg/disc;

Ecological data

This substance is harmful to the environment and it is recommended not to let it enter the environment. Special attention should be paid to the pollution of water bodies.

Molecular structure data

1. Molar refractive index: 58.18

2. Molar volume (cm3/mol): 181.4

3.Isotonic specific volume (90.2K): 476.8

4. Surface tension (dyne/cm): 47.6

5. Polarizability (10-24cm3): 23.06

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): None

2. Number of hydrogen bond donors: 1

3. Number of hydrogen bond acceptors: 3

4. Number of rotatable chemical bonds: 5

5. Number of tautomers: none

6. Topological molecule polar surface area 46.5

7. Number of heavy atoms: 15

8. Surface charge: 0

9. Complexity: 211

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

Avoid contact with oxides.

Storage method

Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Protect from direct sunlight. The packaging is sealed. should be kept away from oxidizer, do not store together. Equipped with the appropriate variety and quantity of fire equipment. Suitable materials should be available in the storage area to contain spills.

Synthesis method

Synthesis of 2,4-D: Sodium phenolate and sodium chloroacetate are first synthesized, and then the two are condensed. The reaction is carried out at 110 to 120°C. The reaction process maintains the slightly alkaline solution. The feeding ratio of monochloroacetic acid to phenol is 1:1.16. Then a chlorination reaction is carried out, using chlorine gas as the chlorinating agent, and the reaction temperature is 92 to 98°C.
It has also been reported that the following operation method is used: After mixing 31.6g of industrial phenol (0.332mol) and an appropriate amount of toluene, the temperature is raised to near the reflux point, and aqueous solutions of sodium hydroxide and chloroacetic acid are added dropwise at the same time. The dropping time is 1 hour, and the reaction is carried out at the reflux temperature. After 1 hour, add 230 mL of tap water to the reaction, separate the organic phase solvent and recycle it to obtain phenoxyacetic acid, which can be directly used for chlorination reaction without distillation operation. Use chlorine gas as the chlorinating agent. Add a trace amount of catalyst (such as iodine powder), the chlorination time is 1 to 3.5 hours, the chlorination temperature is 65 to 90°C, the chlorination is completed by filtering and washing at room temperature, and drying to obtain 57.0g of 2,4-D. The total yield of the two steps is ≥ 76%, the quality is significantly improved.
Synthesis of 2,4-D butyl ester Add wet 2,4-D to a certain amount of butanol under stirring, raise the temperature to 120~140°C, keep it for 4 hours, fully dehydrate, and reflux the butanol. When the water level in the separator no longer rises, stop the reflux, raise the temperature to 160-170°C, and steam out the butanol under reduced pressure.

Purpose

Used as agricultural herbicide.

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