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CHEMISTRY
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ACTIVE PHARMA INGREDIENTS

8 API Suppliers, 1 EU WC, 7 Listed Suppliers, $ API Reference Price

8 API Suppliers
1 EU WC
7 Listed Suppliers
$ API Reference Price

FINISHED DOSAGE FORMULATIONS

1 FDF Dossiers, 1 Listed Dossiers

1 FDF Dossiers
1 Listed Dossiers

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5 APIs

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5 APIs

Synopsis

ACTIVE PHARMA INGREDIENTS

API Suppliers

USDMF

CEP/COS

JDMF

EU WC

KDMF

NDC API

VMF

Listed Suppliers

API REF. PRICE (USD/KG)

$ 67

MARKET PLACE

API

FDF

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Canada

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US Patents

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Health Canada Patents

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Data Compilation #PharmaFlow

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Chemistry

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Also known as: 959-14-8, N,n-diethyl-2-(3-phenyl-1,2,4-oxadiazol-5-yl)ethanamine, Oxolamina, Oksalamin, 683 m, Af 438

Molecular Formula

C₁₄H₁₉N₃O

Molecular Weight

245.32 g/mol

InChI Key

IDCHQQSVJAAUQQ-UHFFFAOYSA-N

FDA UNII

90BEA145GY

Oxolamine is not approved in the USA, it may be marketed elsewhere internationally as a cough suppressant. It is listed as a prescription drug in New Zealand legislation. Oxolamine is also approved in Taiwan for the treatment of respiratory tract inflamation.

1 2D Structure

Oxolamine Citrate

2 Identification

2.1 Computed Descriptors

2.1.1 IUPAC Name

N,N-diethyl-2-(3-phenyl-1,2,4-oxadiazol-5-yl)ethanamine

2.1.2 InChI

InChI=1S/C14H19N3O/c1-3-17(4-2)11-10-13-15-14(16-18-13)12-8-6-5-7-9-12/h5-9H,3-4,10-11H2,1-2H3

2.1.3 InChI Key

IDCHQQSVJAAUQQ-UHFFFAOYSA-N

2.1.4 Canonical SMILES

CCN(CC)CCC1=NC(=NO1)C2=CC=CC=C2

2.2 Other Identifiers

2.2.1 UNII

90BEA145GY

2.3 Synonyms

2.3.1 MeSH Synonyms

1. 5-diethylaminoethyl-3-phenyl-1,2,4-oxadiazole

2. Bredon

3. Oxobron

4. Oxolamine Citrate

5. Oxolamine Monohydrochloride

2.3.2 Depositor-Supplied Synonyms

1. 959-14-8

2. N,n-diethyl-2-(3-phenyl-1,2,4-oxadiazol-5-yl)ethanamine

3. Oxolamina

4. Oksalamin

5. 683 M

6. Af 438

7. Oxadiazole; 683m

8. 5-(2-diethylaminoethyl)-3-phenyl-1,2,4-oxadiazole

9. Af-438 Free Base

10. N,n-diethyl-3-phenyl-1,2,4-oxadiazole-5-ethanamine

11. 90bea145gy

12. Skf 9976 Free Base

13. Skf-9976 Free Base

14. Af-438 [as Citrate]

15. Oxolamine (inn)

16. Skf 9976 [as Citrate]

17. 5-(2-dietilaminoetil)-3-fenil-1,2,4-oxadiazolo

18. Oxolamine [inn]

19. Oxolev

20. Jatan

21. 1,2,4-oxadiazole, 5-(2-(diethylamino)ethyl)-3-phenyl-

22. Oxolev A

23. Ossolamina [dcit]

24. Oxolamina [italian]

25. Ossolamina

26. Oxolaminum

27. Oxolamine [inn:dcf]

28. N,n-diethyl-2-(3-phenyl-1,2,4-oxadiazol-5-yl)ethan-1-amine

29. Oxolaminum [inn-latin]

30. Oxolamina [inn-spanish]

31. Einecs 213-493-4

32. Brn 0527181

33. Unii-90bea145gy

34. Oksalamin (tn)

35. 3-phenyl-5-(beta-diethylaminoethyl)-1,2,4-oxodiazole

36. 5-(2-dietilaminoetil)-3-fenil-1,2,4-oxadiazolo [italian]

37. Oxolamine [mi]

38. Prestwick0_000826

39. Prestwick1_000826

40. Prestwick2_000826

41. Prestwick3_000826

42. Oxolamine [mart.]

43. Ec 213-493-4

44. Oxolamine [who-dd]

45. Bspbio_000751

46. Schembl893333

47. Spbio_002672

48. Bpbio1_000827

49. Zinc1874

50. 1,2,4-oxadiazole-5-ethanamine, N,n-diethyl-3-phenyl-

51. Chembl1620875

52. Dtxsid5023403

53. Chebi:94607

54. Db13216

55. Ncgc00179449-01

56. Sbi-0207016.p001

57. Ft-0748644

58. D07387

59. 959o148

60. Q576684

61. Brd-k42596464-048-03-6

62. 3-phenyl-5-(.beta.-diethylaminoethyl)-1,2,4-oxodiazole

63. N,n-diethyl-2-(3-phenyl-1,2,4-oxadiazol-5-yl)ethanamine 2-hydroxy-1,2,3-propanetricarboxylate

2.4 Create Date

2005-03-26

3 Chemical and Physical Properties

Molecular Formula	C₁₄H₁₉N₃O
Molecular Weight	245.32 g/mol
XLogP3	2.9
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	4
Rotatable Bond Count	6
Exact Mass	245.152812238 g/mol
Monoisotopic Mass	245.152812238 g/mol
Topological Polar Surface Area	42.2 Å²
Heavy Atom Count	18
Formal Charge	0
Complexity	227
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
Covalently Bonded Unit Count	1

4 Pharmacology and Biochemistry

4.1 MeSH Pharmacological Classification

Antitussive Agents

Agents that suppress cough. They act centrally on the medullary cough center. EXPECTORANTS, also used in the treatment of cough, act locally. (See all compounds classified as Antitussive Agents.)

4.2 ATC Code

R - Respiratory system

R05 - Cough and cold preparations

R05D - Cough suppressants, excl. combinations with expectorants

R05DB - Other cough suppressants

R05DB07 - Oxolamine

API SUPPLIERS

01

Gonane Pharma

India

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

Duphat

Not Confirmed

Gonane has API manufacturing expertise in new-age Corticosteroids, Hormones and other pharma raw materials.

Contact Supplier

India

Virtual Booth

Digital Content

USDMF CEP/COS JDMF EU-WC NDC KDMF VMF Others AUDIT

02

Cohance Lifesciences

India

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

Duphat

Not Confirmed

Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.

Contact Supplier

India

Virtual Booth

Digital Content

USDMF CEP/COS JDMF EU-WC

NDC KDMF VMF Others AUDIT

03

Nishchem International Pvt. Ltd

India

Italy

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

Duphat

Not Confirmed

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EU WC

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Listed Suppliers

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API Reference Price

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Number of Transactions

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Quantity (KGS) & Unit rate (USD/KGS) over time

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Importing Country	Total Quantity (KGS)	Average Price (USD/KGS)	Number of Transactions

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ABOUT THIS PAGE

Oxolamine Citrate Manufacturers

A Oxolamine Citrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxolamine Citrate, including repackagers and relabelers. The FDA regulates Oxolamine Citrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxolamine Citrate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

click here to find a list of Oxolamine Citrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Oxolamine Citrate Suppliers

A Oxolamine Citrate supplier is an individual or a company that provides Oxolamine Citrate active pharmaceutical ingredient (API) or Oxolamine Citrate finished formulations upon request. The Oxolamine Citrate suppliers may include Oxolamine Citrate API manufacturers, exporters, distributors and traders.

click here to find a list of Oxolamine Citrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Oxolamine Citrate WC

A Oxolamine Citrate written confirmation (Oxolamine Citrate WC) is an official document issued by a regulatory agency to a Oxolamine Citrate manufacturer, verifying that the manufacturing facility of a Oxolamine Citrate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Oxolamine Citrate APIs or Oxolamine Citrate finished pharmaceutical products to another nation, regulatory agencies frequently require a Oxolamine Citrate WC (written confirmation) as part of the regulatory process.

click here to find a list of Oxolamine Citrate suppliers with Written Confirmation (WC) on PharmaCompass.

Oxolamine Citrate GMP

Oxolamine Citrate Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.

GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).

PharmaCompass offers a list of Oxolamine Citrate GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Oxolamine Citrate GMP manufacturer or Oxolamine Citrate GMP API supplier for your needs.

Oxolamine Citrate CoA

A Oxolamine Citrate CoA (Certificate of Analysis) is a formal document that attests to Oxolamine Citrate's compliance with Oxolamine Citrate specifications and serves as a tool for batch-level quality control.

Oxolamine Citrate CoA mostly includes findings from lab analyses of a specific batch. For each Oxolamine Citrate CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.

Oxolamine Citrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Oxolamine Citrate EP), Oxolamine Citrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Oxolamine Citrate USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.

Find Oxolamine Citrate manufacturers, exporters & distributors on PharmaCompass

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Oxolamine Citrate Manufacturers

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