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ACTIVE PHARMA INGREDIENTS

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US DMFs Filed

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CEP/COS Certifications

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Chemistry

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Also known as: Oxazolazepam, Tranquit, Serenal, Hializan, 24143-17-7, Serenal [japanese]
Molecular Formula
C18H17ClN2O2
Molecular Weight
328.8  g/mol
InChI Key
VCCZBYPHZRWKFY-UHFFFAOYSA-N
FDA UNII
1V2WI2NA1C

Oxazolam
1 2D Structure

Oxazolam

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
10-chloro-2-methyl-11b-phenyl-2,3,5,7-tetrahydro-[1,3]oxazolo[3,2-d][1,4]benzodiazepin-6-one
2.1.2 InChI
InChI=1S/C18H17ClN2O2/c1-12-10-21-11-17(22)20-16-8-7-14(19)9-15(16)18(21,23-12)13-5-3-2-4-6-13/h2-9,12H,10-11H2,1H3,(H,20,22)
2.1.3 InChI Key
VCCZBYPHZRWKFY-UHFFFAOYSA-N
2.1.4 Canonical SMILES
CC1CN2CC(=O)NC3=C(C2(O1)C4=CC=CC=C4)C=C(C=C3)Cl
2.2 Other Identifiers
2.2.1 UNII
1V2WI2NA1C
2.3 Synonyms
2.3.1 MeSH Synonyms

1. 10-chloro-2,3,7,11b-tetrahydro-2-methyl-11b-phenylbenzo(6,7)(1,4)diazepino(5,4-b) Oxazol-6-one

2. Oxazolam, (trans)-isomer

3. Oxazolazepam

2.3.2 Depositor-Supplied Synonyms

1. Oxazolazepam

2. Tranquit

3. Serenal

4. Hializan

5. 24143-17-7

6. Serenal [japanese]

7. 1v2wi2na1c

8. 10-chloro-2,3,7,11b-tetrahydro-2-methyl-11b-phenyloxazolo(3,2-d)(1,4)benzodiazepin-6(5h)-one

9. Benzo(6,7)-1,4-diazepino-(5,4-b)-oxazol-6-one, 10-chloro-2,3,5,6,7,11b-hexahydro-2-methyl-11b-phenyl-

10. Oxazolo[3,2-d][1,4]benzodiazepin-6(5h)-one, 10-chloro-2,3,7,11b-tetrahydro-2-methyl-11b-phenyl-

11. Oxazolamum

12. Convertal

13. 10-chloro-2,3,7,11b-tetrahydro-2-methyl-11b-phenyloxazolo[3,2-d][1,4]benzodiazepin-6(5h)-one

14. Oxazolo(3,2-d)(1,4)benzodiazepin-6(5h)-one, 10-chloro-2,3,7,11b-tetrahydro-2-methyl-11b-phenyl-

15. Oxazolam [inn:jan]

16. Oxazolamum [inn-latin]

17. Unii-1v2wi2na1c

18. 27167-30-2

19. Einecs 246-032-0

20. Serenal (tn)

21. Cs 300

22. Oxazolam [inn]

23. Oxazolam [jan]

24. Oxazolam [mi]

25. Oxazolam (jp17/inn)

26. Oxazolam [mart.]

27. Oxazolam [who-dd]

28. Estrone3-hemisuccinate

29. Dea No. 2839

30. Chembl2104805

31. Dtxsid5023401

32. Schembl10619798

33. Chebi:31944

34. Akos030242155

35. Db15491

36. (cis,trans)-10-chlor-2,3,5,6,7,11b-tetrahydro-2-methyl-11b-phenyloxazolo(3,2-d)(1,4)benzodiazepin-6(5h)-on

37. 10-chloro-2-methyl-11b-phenyl-2,3,5,7-tetrahydro-[1,3]oxazolo[3,2-d][1,4]benzodiazepin-6-one

38. Oxazolo[3,2-d][1,4]benzodiazepin-6(5h)-one,10-chloro-2,3,7,11b-tetrahydro-2-methyl-11b-phenyl-

39. D01278

40. 167o302

41. 10-chloro-2,3,5,11b-tetrahydro-2-methyl-11b-phenyloxazolo[3,2-d][1,4]benzodiazepin-6(7h)-one

42. 10-chloro-2-methyl-11b-phenyl-2,3,7,11b-tetrahydro[1,3]oxazolo[3,2-d][1,4]benzodiazepin-6(5h)-one #

2.4 Create Date
2005-03-25
3 Chemical and Physical Properties
Molecular Weight 328.8 g/mol
Molecular Formula C18H17ClN2O2
XLogP33
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count1
Exact Mass328.0978555 g/mol
Monoisotopic Mass328.0978555 g/mol
Topological Polar Surface Area41.6 Ų
Heavy Atom Count23
Formal Charge0
Complexity468
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count2
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count1

API SUPPLIERS

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API Reference Price

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29-Jan-2021
12-Jun-2022
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ABOUT THIS PAGE

Oxazolam Manufacturers

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

Oxazolam Suppliers

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

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

Oxazolam JDMF

The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.

The Oxazolam Drug Master File in Japan (Oxazolam JDMF) empowers Oxazolam API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).

PMDA reviews the Oxazolam JDMF during the approval evaluation for pharmaceutical products. At the time of Oxazolam JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.

click here to find a list of Oxazolam suppliers with JDMF on PharmaCompass.

Oxazolam GMP

Oxazolam 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 Oxazolam 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 Oxazolam GMP manufacturer or Oxazolam GMP API supplier for your needs.

Oxazolam CoA

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

Oxazolam CoA mostly includes findings from lab analyses of a specific batch. For each Oxazolam 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.

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