Kimia Biosciences

(2S)-2-aminobutanamide;hydrochloride

Chemistry, 8 End Use API, 26 Related Intermediates

Manufacturers/Suppliers

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8 Suppliers

Also known as: 7682-20-4, (s)-2-aminobutyramide hydrochloride, H-abu-nh2 hcl, (s)-2-aminobutanamide hydrochloride, L-2-aminobutanamide hydrochloride, (s)-(+)-2-aminobutanamide hydrochloride

Molecular Formula

C₄H₁₁ClN₂O

Molecular Weight

138.59 g/mol

InChI Key

HDBMIDJFXOYCGK-DFWYDOINSA-N

FDA UNII

2C1V4527RJ

1 2D Structure

(2S)-2-aminobutanamide;hydrochloride

2 Identification

2.1 Computed Descriptors

2.1.1 IUPAC Name

(2S)-2-aminobutanamide;hydrochloride

2.1.2 InChI

InChI=1S/C4H10N2O.ClH/c1-2-3(5)4(6)7;/h3H,2,5H2,1H3,(H2,6,7);1H/t3-;/m0./s1

2.1.3 InChI Key

HDBMIDJFXOYCGK-DFWYDOINSA-N

2.1.4 Canonical SMILES

CCC(C(=O)N)N.Cl

2.1.5 Isomeric SMILES

CC[C@@H](C(=O)N)N.Cl

2.2 Other Identifiers

2.2.1 UNII

2C1V4527RJ

2.3 Synonyms

2.3.1 Depositor-Supplied Synonyms

1. 7682-20-4

2. (s)-2-aminobutyramide Hydrochloride

3. H-abu-nh2 Hcl

4. (s)-2-aminobutanamide Hydrochloride

5. L-2-aminobutanamide Hydrochloride

6. (s)-(+)-2-aminobutanamide Hydrochloride

7. (2s)-2-aminobutanamide;hydrochloride

8. L-2-aminobutanamide, Hcl

9. Butanamide, 2-amino-, Monohydrochloride, (2s)-

10. L-homoalanylamide Hcl

11. 141978-61-2

12. 2c1v4527rj

13. Levetiracetam Related Compound B [usp-rs]

14. Butanamide, 2-amino-, Monohydrochloride, (s)-

15. Butanamide, 2-amino-, Hydrochloride (1:1), (2s)-

16. H-abu(2)-nh2 Hcl

17. (s)-2-aminobutanamide Hcl

18. (s)-2-amino Butanamide Hcl

19. (s)-2-amino-butanamide Hcl

20. Mfcd00136565

21. H-abu-nh2hcl

22. (s)-2-amino-butanamide Hydrochloride

23. S (+)-2-aminobutyramide Hydrochloride

24. L-2-aminobutanamide Hcl

25. Schembl373444

26. Unii-2c1v4527rj

27. L-homoalanylamide Hydrochloride

28. (s)-2-amino-butylactamide Hcl

29. Dtxsid10474839

30. S-2-aminobutanamide Hydrochloride

31. Act02761

32. Cs-b0864

33. H-abu-nh2 Hydrochloride, Aldrichcpr

34. Akos015910759

35. Ds-1209

36. Butanamide,2-amino-,hydrochloride(1:1)

37. Ac-23986

38. Am20100759

39. (s)-2-aminobutanamide Hydrochloride [usp-rs]

40. (s)-(+)-2-aminobutanamide Hydrochloride, 97%

41. 682a204

42. A935960

43. (2s)-2-aminobutanamide--hydrogen Chloride (1/1)

44. Butyramide, 2-amino-, Monohydrochloride, L-

45. Q-102786

46. Levetiracetam Related Compound B, United States Pharmacopeia (usp) Reference Standard

2.4 Create Date

2006-12-11

3 Chemical and Physical Properties

Molecular Formula	C₄H₁₁ClN₂O
Molecular Weight	138.59 g/mol
Hydrogen Bond Donor Count	3
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	2
Exact Mass	138.0559907 g/mol
Monoisotopic Mass	138.0559907 g/mol
Topological Polar Surface Area	69.1 Å²
Heavy Atom Count	8
Formal Charge	0
Complexity	72.1
Isotope Atom Count	0
Defined Atom Stereocenter Count	1
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
Covalently Bonded Unit Count	2

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CAS Number

63095-51-2

End Use API

Kimia Biosciences, established in 1993, is focused on manufacturing bulk drugs for various therapeutic se...

Kimia Biosciences, established in 1993, is focused on manufacturing bulk drugs for various therapeutic segments. With a strong emphasis on excellence and advanced technologies, Kimia aims to become a globally recognized company in both APIs and FDFs while upholding clean business practices. Kimia's state-of-the-art facilities at Village Bhondsi, Gurugram enable it to produce a wide range of APIs. Kimia also plans to establish its own facilities for lifestyle segments, adhering to international regulatory standards. Kimia aims to provide the best pharmaceutical products and support to consumers and healthcare professionals.

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