Please Wait
Applying Filters...
menu
    • menu
    Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

    Virtual Booth

    Contact Supplier

    Jai Radhe Sales is your partner for all your sourcing needs.

    Virtual Booth

    Contact Supplier

    xyz-pharma-m-2024-10-07

    Virtual Booth

    Contact Supplier

    Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.

    Virtual Booth

    Contact Supplier

    Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.

    Virtual Booth

    Contact Supplier

    xyz-pharma-m-2024-10-07

    Virtual Booth

    Contact Supplier

    Menu

    Suxamethonium Chloride Dihydrate

    DIGITAL CONTENT

    PharmaCompass
    Xls

    Filters

    clear-filterReset all filters
    2D Structure
    Also known as: 6101-15-1, Suxamethonium chloride dihydrate, Choline chloride succinate, Suxamethonium chloride, Suxamethonium chloride hydrate, Succinyldicholine dichloride
    Molecular Formula
    C14H34Cl2N2O6
    Molecular Weight
    397.3  g/mol
    InChI Key
    FFSBEIRFVXGRPR-UHFFFAOYSA-L
    FDA UNII
    8L0S1G435E
    A quaternary skeletal muscle relaxant usually used in the form of its bromide, chloride, or iodide. It is a depolarizing relaxant, acting in about 30 seconds and with a duration of effect averaging three to five minutes. Succinylcholine is used in surgical, anesthetic, and other procedures in which a brief period of muscle relaxation is called for.
    1 2D Structure

    2D Structure

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    trimethyl-[2-[4-oxo-4-[2-(trimethylazaniumyl)ethoxy]butanoyl]oxyethyl]azanium;dichloride;dihydrate
    2.1.2 InChI
    InChI=1S/C14H30N2O4.2ClH.2H2O/c1-15(2,3)9-11-19-13(17)7-8-14(18)20-12-10-16(4,5)6;;;;/h7-12H2,1-6H3;2*1H;2*1H2/q+2;;;;/p-2
    2.1.3 InChI Key
    FFSBEIRFVXGRPR-UHFFFAOYSA-L
    2.1.4 Canonical SMILES
    C[N+](C)(C)CCOC(=O)CCC(=O)OCC[N+](C)(C)C.O.O.[Cl-].[Cl-]
    2.2 Other Identifiers
    2.2.1 UNII
    8L0S1G435E
    2.3 Synonyms
    2.3.1 MeSH Synonyms

    1. Anectine

    2. Bromide, Suxamethonium

    3. Celocurine

    4. Dibromide, Succinylcholine

    5. Dichloride, Succinylcholine

    6. Dicholine Succinate

    7. Diiodide, Succinylcholine

    8. Diperchlorate, Succinylcholine

    9. Ditilin

    10. Listenon

    11. Lysthenon

    12. Myorelaxin

    13. Quelicin

    14. Succicuran

    15. Succinate, Dicholine

    16. Succinylcholine

    17. Succinylcholine Chloride

    18. Succinylcholine Dibromide

    19. Succinylcholine Dichloride

    20. Succinylcholine Dichloride, Di H2o

    21. Succinylcholine Dichloride, Di-h2o

    22. Succinylcholine Diiodide

    23. Succinylcholine Diperchlorate

    24. Succinylcholine Iodide

    25. Succinyldicholine

    26. Suxamethonium

    27. Suxamethonium Bromide

    28. Suxamethonium Chloride

    2.3.2 Depositor-Supplied Synonyms

    1. 6101-15-1

    2. Suxamethonium Chloride Dihydrate

    3. Choline Chloride Succinate

    4. Suxamethonium Chloride

    5. Suxamethonium Chloride Hydrate

    6. Succinyldicholine Dichloride

    7. Suxamethonium Chloride Hydrate [jan]

    8. 8l0s1g435e

    9. 6101-15-1 (chloride Dihydrate)

    10. Ethanaminium, 2,2'-((1,4-dioxo-1,4-butanediyl)bis(oxy))bis(n,n,n-trimethyl-), Dichloride, Dihydrate

    11. 2,2'-(succinylbis(oxy))bis(n,n,n-trimethylethan-1-aminium) Chloride Dihydrate

    12. Unii-8l0s1g435e

    13. Mfcd00150564

    14. Succin (tn)

    15. Suxamethonium Chloride 2h2o

    16. Succinylcholine Chloride 2h2o

    17. Succinylbischolinchloriddihydrat

    18. Chebi:61225

    19. Dtxsid50976488

    20. Hms3887k13

    21. Succinylcholine Dichloride Dihydrate

    22. Succinylcholine (chloride Dihydrate)

    23. S4121

    24. Succinyldicholine Dichloride Dihydrate

    25. Akos024462531

    26. Ccg-268618

    27. Suxamethonium Chloride [who-ip]

    28. Suxamethonium Chloride Hydrate (jp17)

    29. S10403

    30. Succinylcholine Chloride [who-ip]

    31. Ac-33148

    32. As-13333

    33. Trimethyl-[2-[4-oxo-4-[2-(trimethylazaniumyl)ethoxy]butanoyl]oxyethyl]azanium;dichloride;dihydrate

    34. Db-053765

    35. B1595

    36. Ft-0635981

    37. Suxamethonii Chloridum [who-ip Latin]

    38. D02275

    39. Suxamethonium Chloride Dihydrate [who-dd]

    40. A837139

    41. Q-201774

    42. Q27130900

    43. Succinylcholine Chloride Dihydrate, 98.0-102.0%, Solid

    44. Suxamethonium Chloride, European Pharmacopoeia (ep) Reference Standard

    45. 2,2'-succinyldioxybis(ethyltrimethylammonium) Dichloride, Dihydrate [who-ip]

    46. Succinylcholine Chloride, United States Pharmacopeia (usp) Reference Standard

    47. 2,2'-[(1,4-dioxobutane-1,4-diyl)bis(oxy)]bis(n,n,n-trimethylethanaminium) Chloride--water (1/2)

    48. 2-[1,4-dioxo-4-[2-(trimethylammonio)ethoxy]butoxy]ethyl-trimethylammonium Dichloride Dihydrate

    49. Succin Succin (tn) Suxamethonium Chloride Succinylcholine Chloride Suxamethonium Chloride (jp15) Suxamethonium Chloride Dihydrate Cid656867 D02275 (2-hydroxyethyl)trimethylammonium Chloride Succinate 6101-15-1 71-27-2

    50. Trimethyl-[2-[4-oxidanylidene-4-[2-(trimethylazaniumyl)ethoxy]butanoyl]oxyethyl]azanium Dichloride Dihydrate

    2.4 Create Date
    2005-06-24
    3 Chemical and Physical Properties
    Molecular Weight 397.3 g/mol
    Molecular Formula C14H34Cl2N2O6
    Hydrogen Bond Donor Count2
    Hydrogen Bond Acceptor Count8
    Rotatable Bond Count11
    Exact Mass396.1793922 g/mol
    Monoisotopic Mass396.1793922 g/mol
    Topological Polar Surface Area54.6 Ų
    Heavy Atom Count24
    Formal Charge0
    Complexity284
    Isotope Atom Count0
    Defined Atom Stereocenter Count0
    Undefined Atom Stereocenter Count0
    Defined Bond Stereocenter Count0
    Undefined Bond Stereocenter Count0
    Covalently Bonded Unit Count5
    4 Pharmacology and Biochemistry
    4.1 MeSH Pharmacological Classification

    Neuromuscular Depolarizing Agents

    Drugs that interrupt transmission at the skeletal neuromuscular junction by causing sustained depolarization of the motor end plate. These agents are primarily used as adjuvants in surgical anesthesia to cause skeletal muscle relaxation. (See all compounds classified as Neuromuscular Depolarizing Agents.)