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Chemistry

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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

Suxamethonium Chloride Dihydrate
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

Suxamethonium Chloride Dihydrate

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.)


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