Epoxy curing agent Knowledge Piperidolate Hydrochloride Piperidolate Hydrochloride

Piperidolate Hydrochloride Piperidolate Hydrochloride

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Peridoester Hydrochloride Structural Formula

Structural formula

Business number 03M6
Molecular formula C21H26ClNO2
Molecular weight 359.90
label

Diheperdone,

aromatic compounds

Numbering system

CAS number:129-77-1

MDL number:MFCD00057377

EINECS number:204-964-5

RTECS number:None

BRN number:None

PubChem ID:None

Physical property data

1. Characteristics: colorless flammable liquid.


2. Density (g/mL ,25/4℃): 0.7681


3. Refractive index (n D20): 1.3900


4. Flashpoint ():-15


5. Melting point ():-112


6. Boiling point (ºC):83


7. Solubility:Easily soluble in ethanol and ether, slightly soluble in water.


8. Stability:Chemically active, easy to undergo addition and polymerization reactions, easily hydrolyzed by acids into acetaldehyde and Isobutanol.

Toxicological data


1, acute toxicity: rat intravenously LD5O: 19mg/kg


Mice orally LD5O: 1040mg/kg


Mouse transvenous LD5O: 26mg/kg


Dog Meridian VeinLD5O35mg/kg



Ecological data

None yet

Molecular structure data

None yet

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: 6

5. Number of tautomers: none

6. Topological molecule polar surface area 29.5

7. Number of heavy atoms: 25

8. Surface charge: 0

9. Complexity: 367

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 1

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 2

Properties and stability

None yet

Storage method

None yet

Synthesis method

Introduction to production methods

Produced by the base-catalyzed addition of acetylene and isobutanol.

Purpose

Usage

Used as polymer monomer and organic synthesis intermediate.

AMILY: Times New Roman; mso-list: Ignore”>8. Stability:Reactive chemical properties, prone to addition and polymerization reactions, and easily hydrolyzed by acids into acetaldehyde and isobutanol.

Toxicological data


1, acute toxicity: rat intravenously LD5O: 19mg/kg


Mice orally LD5O: 1040mg/kg


Mouse transvenous LD5O: 26mg/kg


Dog Meridian VeinLD5O35mg/kg



Ecological data

None yet

Molecular structure data

None yet

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: 6

5. Number of tautomers: none

6. Topological molecule polar surface area 29.5

7. Number of heavy atoms: 25

8. Surface charge: 0

9. Complexity: 367

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 1

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 2

Properties and stability

None yet

Storage method

None yet

Synthesis method

Introduction to production methods

Produced by the base-catalyzed addition of acetylene and isobutanol.

Purpose

Usage

Used as polymer monomer and organic synthesis intermediate.

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