Atropine sulfate

Base Information

  • PRODUCT:Atropine sulfate
  • CAS.:55-48-1
  • MF:2(C17H23NO3).H2SO4
  • Molecular Weight:387.454
  • Purity:99%

Product Details

CAS: 55-48-1

MF: 2(C17H23NO3).H2SO4

Appearance: White crystalline powder

Export Top Purity Atropine sulfate 55-48-1 In Stock

  • Molecular Formula:C17H23NO3*H2O4S
  • Molecular Weight:387.454
  • Appearance/Colour:White crystalline powder 
  • Vapor Pressure:9.1E-28mmHg at 25°C 
  • Melting Point:189-192 °C (A)(lit.) 
  • Refractive Index:1.6900 (estimate) 
  • Boiling Point:806.7 °C at 760 mmHg 
  • Flash Point:441.7 °C 
  • PSA:182.52000 
  • Density:1.1172 (rough estimate) 
  • LogP:4.16560 

Atropine sulfate(Cas 55-48-1) Usage

General Description

Atropine sulfate is a drug that blocks nerve stimulation of muscles and glands, and relaxes smooth muscles. Atropine sulfate is a type of antimuscarinic agent and tropane alkaloid. It's derived from the naturally-occurring alkaloid atropine, which comes from the Atropa belladonna plant.
Uses Atropine sulfate is one of the major lifesaving antidotes given for OP poisoning and acts by neutralizing the acetylcholine-like action of these chemical agents as a physiologic antagonist . It is generally given for SLUDGE (salivation, lacrimation, urination, diaphoresis, gastrointestinal motility, emesis) symptoms caused by organophosphate poisoning.

Safety Profile

Poison by subcutaneous, intravenous, and intraperitoneal routes. Moderately toxic by ingestion. Human (child) pulmonary system effects by ingestion. Human systemic effects: decreased body temperature, cardiac arrhythmias. An experimental teratogen. Other experimental reproductive effects. See also ATROPINE. When heated to decomposition it emits very toxic fumes of NO,xand SOx.

Handling Avoid inhaling vapors or mists, swallowing, and prolonged or repeated skin contact. Wear safety glasses with side shields or goggles.

Veterinary Drugs and Treatments

The principal veterinary indications for systemic atropine include: !!Preanesthetic to prevent or reduce secretions of the respiratory tract !!Treat sinus bradycardia, sinoatrial arrest, and incomplete AV block !!Differentiate vagally-mediated bradycardia for other causes !!As an antidote for overdoses of cholinergic agents (e.g., physostigmine, etc.) !!As an antidote for organophosphate, carbamate, muscarinic mushroom, blue-green algae intoxication !!Hypersialism !!Treatment of bronchoconstrictive disease

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InChI:InChI=1/2C17H23NO3.H2O4S/c2*1-18-13-7-8-14(18)10-15(9-13)21-17(20)16(11-19)12-5-3-2-4-6-12;1-5(2,3)4/h2*2-6,13-16,19H,7-11H2,1H3;(H2,1,2,3,4)/t2*13-,14+,15+,16?;

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55-48-1 Relevant articles

Preparing for Chemical Terrorism: Stability of Injectable Atropine Sulfate

Joshua G. Schier MD, Padinjarekuttu R. Ravikumar PhD, Lewis S. Nelson MD, Michael B. Heller MD, Mary Ann Howland PharmD, Robert S. Hoffman MD

, AEM, Volume11, Issue4 April 2004 Pages 329-334

his was an in-vitro study using gas chromatography and mass spectrometry (GC/MS). Four atropine solutions (labeled concentration of 400 μg/mL) ranging from in date to 12 years beyond expiration (exp) and an additional sample of atropine sulfate (labeled concentration of 2,000 μg/mL) obtained from a World War II era autoinjector were assayed for atropine stability. Standards of atropine sulfate and tropine were prepared and quantified by GC/MS.

Clinical and bioavailability studies of sublingually administered atropine sulfate

Sheetal Rajpal MPharm b , Raisuddin Ali MPharm a , Aseem Bhatnagar MD a , Sujit Kumar Bhandari MDS a , Gaurav Mittal PhD a

, The American Journal of Emergency Medicine Volume 28, Issue 2, February 2010, Pages 143-150

The objectives of the present study were to develop a novel atropine sulfate (AS) sublingual injection formulation, to create its bioavailability data in humans and to evaluate its suitability for field use with a view to obtain early therapeutic drug concentration in comparison to the conventional intramuscular route that provides a therapeutic peak of 6 to 8 ng/mL in blood at 30 minutes.

55-48-1 Process route

Atropine
51-55-8

Atropine

atropine sulfate
5908-99-6,55-48-1,300-40-3,620-61-1,1867-24-9,2472-17-5,2623-69-0,14844-27-0

atropine sulfate

Conditions
Conditions Yield
With sulfuric acid; In dichloromethane; water; acetone; at 29 - 42 ℃; for 3.5h;
85 g
α-formyl phenyl acetic acid
59216-85-2

α-formyl phenyl acetic acid

atropine sulfate
5908-99-6,55-48-1,300-40-3,620-61-1,1867-24-9,2472-17-5,2623-69-0,14844-27-0

atropine sulfate

Conditions
Conditions Yield
Multi-step reaction with 3 steps
1: sodium methylate / toluene / 5 h / 109 - 115 °C
2: sodium tetrahydroborate; methanol / dichloromethane / 4 h / 0 - 20 °C
3: sulfuric acid / water; dichloromethane; acetone / 3.5 h / 29 - 42 °C
With methanol; sodium tetrahydroborate; sulfuric acid; sodium methylate; In dichloromethane; water; acetone; toluene;
 

55-48-1 Upstream products

  • 59216-85-2
    59216-85-2

    α-formyl phenyl acetic acid

  • 51-55-8
    51-55-8

    Atropine

  • 542-05-2
    542-05-2

    acetonedicarboxylic acid

  • 532-24-1
    532-24-1

    tropinone

55-48-1 Downstream products

  • 16839-98-8
    16839-98-8

    Noratropine

  • 100-52-7
    100-52-7

    benzaldehyde

  • 120-29-6
    120-29-6

    3-tropanol

  • 13269-35-7
    13269-35-7

    (+)-Atropine

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