Epoxy curing agent Knowledge 2,6-dimethylmorpholine

2,6-dimethylmorpholine

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2,6-dimethylmorpholine structural formula

Structural formula

Business number 03UH
Molecular formula C6H13NO
Molecular weight 115
label

None yet

Numbering system

CAS number:141-91-3

MDL number:MFCD00005973

EINECS number:205-509-3

RTECS number:QE1750000

BRN number:103036

PubChem ID:None

Physical property data

1. Physical property data:

1.Character: colorless liquid

2.Melting point (℃): -85

3.Boiling point (ºC): 147

4.Relative density: 0.935

5.Relative vapor density (g/mL,Air= 1): 4.0

6.Flash point (℃): 44.4

7.Water-soluble (g/100mL, 19°C): >=0.01

8.Solubility: Easily soluble in water, easily soluble in ethanol, soluble in acetone, miscible in benzene.

Toxicological data

2. Toxicological data:

1, acute toxicity: rat oral LD50: 2830 mg/kg;

Rabbit transdermalLD50710 uL/kg

2, Inhalation toxicity: RatLC: >4000ppm/4H

Ecological data

3. Ecology Data:

1. Other harmful effects: This substance may be harmful to the environment, and special treatment should be given to water bodies. Notice.

Molecular structure data

5. Molecular property data:

1. Molar refractive index:32.72

2. Molar volume (cm3/mol): 131.9

3. Isotonic specific volume (90.2K ):300.6

4. Surface tension (dyne/ cm):26.9

5. Polarizability10-24cm3):12.97

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): 0.3

2. Number of hydrogen bond donors: 1

3. Number of hydrogen bond acceptors: 2

4. Number of rotatable chemical bonds: 0

5. Number of tautomers: none

6. Topological molecule polar surface area 21.3

7. Number of heavy atoms: 8

8. Surface charge: 0

9. Complexity: 66.9

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 2

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

Stable under normal temperature and pressure.

Incompatible materials:Strong oxidants, strong acids

Storage method

Keep sealed.

Synthesis method

):131.9

3. Isotonic specific volume (90.2K ):300.6

4. Surface tension (dyne/ cm):26.9

5. Polarizability10-24cm3):12.97

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): 0.3

2. Number of hydrogen bond donors: 1

3. Number of hydrogen bond acceptors: 2

4. Number of rotatable chemical bonds: 0

5. Number of tautomers: none

6. Topological molecule polar surface area 21.3

7. Number of heavy atoms: 8

8. Surface charge: 0

9. Complexity: 66.9

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 2

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

Stable under normal temperature and pressure.

Incompatible materials:Strong oxidants, strong acids

Storage method

Keep sealed.

Synthesis method

The preparation method is composed of two– (2-Hydroxypropyl) Amine hydrochloride is obtained by thermal dehydration with concentrated sulfuric acid, and then alkali is added to precipitate2,6 –Dimethylmorpholine is distilled to obtain the finished product.

Purpose

1.Used as corrosion inhibitor, stabilizer for chlorinated solvents, rubber accelerator, insecticide and for fabric treatment.

2.2,6-Dimethylmorpholine is an intermediate of the fungicide fenpropimorph.

ottom-alt: auto; mso-pagination: widow-orphan” align=”left”>The preparation method is as follows: -(2-Hydroxypropyl)Amine hydrochloride is obtained by thermal dehydration with concentrated sulfuric acid, and then alkali is added to precipitate2,6-Dimethylmorpholine, distilled to obtain the finished product.

Purpose

1.Used as corrosion inhibitor, stabilizer for chlorinated solvents, rubber accelerator, insecticide and for fabric treatment.

2.2,6-Dimethylmorpholine is an intermediate of the fungicide fenpropimorph.

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