atropine

Date：2024-05-07 Categories：News

Atropine structural formula

Structural formula

Physical competition number	0150
Molecular formula	C9H23NO3
Molecular weight	289.37
label	(8-Methyl-8-azabicyclo[3.2.1]oct-3-yl) 3-hydroxy-2-phenyl-propionate, belladonnaine, Solanine, m-methoxybenzaldehyde, 3-Methoxybenzaldehyde, Solanin, solanine, Eggplant spirit, Hyoscyamine, Tropine tropate, endo-(±)-α-(Hydroxymethyl)benzeneacetic acid 8-methyl-8-azabicyclo[3.2.1]oct-3-yl ester

Numbering system

CAS number:51-55-8

MDL number:MFCD00022622

EINECS number:200-104-8

RTECS number:CK0700000

BRN number:91260

PubChem number:24890401

Physical property data

1. Properties: White needle-like crystals. Sensitive to light and air. Sublime at 93-110℃ in high vacuum. 2. Density (g/mL, 25/4℃): Not determined

3. Relative vapor density (g/mL, air=1): Not determined

4. Melting point (ºC): 2855. Boiling point (ºC, normal pressure): Undetermined

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

7. Refractive index: Undetermined

8. Flash point ( ºC): Undetermined

9. Specific optical rotation (º): Undetermined

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

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

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

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

14. Critical temperature (ºC): Undetermined

15. Critical pressure (KPa): Undetermined

16. Oil and water (octanol/ Log value of the distribution coefficient (water): Undetermined

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

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

19. Solubility: 1g is soluble in 455ml water, 90ml 80℃ water, 2ml ethanol, 1.2ml 60℃ ethanol, 27ml glycerol, 25ml ether and 1ml chloroform, also soluble in benzene and dilute acid. The pH of a 0.0015mol/L solution is 10.0

Toxicological data

1. Acute toxicity: Rat oral LD50: 500mg/kg

Mouse oral LD50: 75mg/kg

Ecological data

1. Other harmful effects: This substance may be harmful to the environment, and special attention should be paid to water bodies.

Molecular structure data

1. MooreEmissivity: 80.78

2. Molar volume (cm³/mol): 242.4

3. Isotonic specific volume (90.2K): 646.1

4. Surface tension (dyne/cm): 50.4

5. Polarizability (10-24cm3): 32.02

Compute chemical data

1. Hydrophobic parameter calculation reference value (XlogP): 1.8

2. Number of hydrogen bond donors: 1

3. Number of hydrogen bond acceptors: 4

4. Number of rotatable chemical bonds: 5

5. Number of tautomers:

6. Topological molecular polar surface area (TPSA): 49.8

7. Number of heavy atoms: 21

8. Surface charge: 0

9. Complexity: 353

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 2

12. Uncertain number of atomic stereocenters: 1

13. Determine the number of chemical bond stereocenters Number: 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

Avoid light, open flame, and high temperature

Storage method

Filled with argon, sealed at 0 degrees Celsius, and stored in a dry place away from light.

Synthesis method

Hyoscyamine (L-body) is extracted from belladonna leaves, and then refined through racemization and recrystallization. It can also be obtained artificially.

Purpose

Atropine is a parasympathetic nerve inhibitor that can be used as an eye dilator and laxative; it can relieve hay fever, cold nasal obstruction and intestinal spasm; it can be used to treat nocturia in children, and is sometimes used to relieve ureteral and bile duct spasm; and It can be used to treat poisoning caused by organophosphorus. As an anticholinergic drug, atropine’s various pharmacological effects are not conducive to its clinical application. Some substitutes with specific effects have been synthesized, such as homatropine as a pupil dilator. Atropine is highly toxic and can cause blurred vision, stasis of secretion, vasodilation, high fever, excitement, agitation and delirium when the dose is too high. It is an antagonist of morphine, pilocarpine, physostigmine, etc.

Biochemical research. A reagent for assaying gold.

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