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Also known as: 183204-72-0, Tipiracil hcl, Tipiracil (hydrochloride), Tipiracil hydrochloride [usan], Tas-1-462, 4h59klq0a4
Molecular Formula
C9H12Cl2N4O2
Molecular Weight
279.12  g/mol
InChI Key
KGHYQYACJRXCAT-UHFFFAOYSA-N
FDA UNII
4H59KLQ0A4

Tipiracil Hydrochloride
1 2D Structure

Tipiracil Hydrochloride

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
5-chloro-6-[(2-iminopyrrolidin-1-yl)methyl]-1H-pyrimidine-2,4-dione;hydrochloride
2.1.2 InChI
InChI=1S/C9H11ClN4O2.ClH/c10-7-5(12-9(16)13-8(7)15)4-14-3-1-2-6(14)11;/h11H,1-4H2,(H2,12,13,15,16);1H
2.1.3 InChI Key
KGHYQYACJRXCAT-UHFFFAOYSA-N
2.1.4 Canonical SMILES
C1CC(=N)N(C1)CC2=C(C(=O)NC(=O)N2)Cl.Cl
2.2 Other Identifiers
2.2.1 UNII
4H59KLQ0A4
2.3 Synonyms
2.3.1 Depositor-Supplied Synonyms

1. 183204-72-0

2. Tipiracil Hcl

3. Tipiracil (hydrochloride)

4. Tipiracil Hydrochloride [usan]

5. Tas-1-462

6. 4h59klq0a4

7. 5-chloro-6-((2-iminopyrrolidin-1-yl)methyl)pyrimidine-2,4(1h,3h)-dione Hydrochloride

8. Chembl65375

9. Ma-1 Hydrochloride

10. Tpi

11. Unii-4h59klq0a4

12. Tipiracil.hcl

13. 5-chloro-6-[(2-iminopyrrolidin-1-yl)methyl]pyrimidine-2,4(1h,3h)-dione Hydrochloride

14. Tipiracilhydrochloride

15. Tipiracil Monohydrochloride

16. 5-chloro-6-[(2-iminopyrrolidin-1-yl)methyl]-1h-pyrimidine-2,4-dione;hydrochloride

17. Schembl1682924

18. Chebi:90877

19. Ex-a882

20. Dtxsid001027748

21. Amy25415

22. Bcp06245

23. Ex-a1393

24. Hy-a0063

25. Tipiracil Hydrochloride (jan/usan)

26. Tipiracil Hydrochloride [mi]

27. Mfcd01571384

28. S3731

29. Tipiracil Hydrochloride [jan]

30. Akos027427002

31. Ccg-267234

32. Cs-1637

33. Tipiracil Hydrochloride [who-dd]

34. 2,4(1h,3h)-pyrimidinedione,5-chloro-6-[(2-imino-1-pyrrolidinyl)methyl]-, Hydrochloride (1:1)

35. Ac-30634

36. As-56082

37. Tipiracil Hydrochloride, >=98% (hplc)

38. Db-065426

39. Ft-0700247

40. Tipiracil Hydrochloride [orange Book]

41. A13098

42. D10467

43. Lonsurf Component Tipiracil Hydrochloride

44. A847265

45. S-95005 Component Tipiracil Hydrochloride

46. Tas-102 Component Tipiracil Hydrochloride

47. Tipiracil Hydrochloride Component Of Lonsurf

48. J-690251

49. Q27162848

50. 5-chloro-6-(1-(2-iminopyrrolidinyl)methyl)uracil Hydrochloride

51. 5-chloro-6-(1-(2-iminopyrrolidinyl)-methyl)uracil Hydrochloride

52. 2,4(1h,3h)-pyrimidinedione,5-chloro-6-[(2-imino-1-pyrrolidinyl)methyl] Hydrochloride

53. 5-chloro-6-((2-iminopyrrolidin-1-yl)methyl)pyrimidine-2,4(1h,3h)-dione Hcl

54. 5-chloro-6-((2-iminopyrrolidin-1-yl)methyl)pyrimidine-2,4(1h,3h)-dionehydrochloride

55. 5-chloro-6-(2-iminopyrrolidin-1-yl)methyl-2,4(1h,3h)-pyrimidinedione Hydrochloride

56. 5-chloro-6-(2-iminopyrrolidin-1-yl)methyl-2,4-(1h,3h)-pyrimidinedione Hydrochloride

57. 1-[(5-chloro-2,6-dioxo-1,2,3,6-tetrahydropyrimidin-4-yl)methyl]pyrrolidin-2-iminium Chloride

58. 2,4(1h,3h)-pyrimidinedione, 5-chloro-6-((2-imino-1-pyrrolidinyl)methyl)-, Hydrochloride (1:1)

59. 5-chloro-6-((2-iminopyrrolidin-1-yl)methyl)pyrimidine-2,4(1h,3h)-dione Hydrochloride;tipiracil Hcl

60. 5-chloro-6-(2-imino-pyrrolidin-1-yl)methyl-2,4(1h,3h)-pyrimidinedione Hydrochloride

2.4 Create Date
2006-10-25
3 Chemical and Physical Properties
Molecular Weight 279.12 g/mol
Molecular Formula C9H12Cl2N4O2
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count3
Rotatable Bond Count2
Exact Mass278.0337310 g/mol
Monoisotopic Mass278.0337310 g/mol
Topological Polar Surface Area85.3 Ų
Heavy Atom Count17
Formal Charge0
Complexity404
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count2

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16-Aug-2024
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ABOUT THIS PAGE

Tipiracil Hydrochloride Manufacturers

A Tipiracil Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tipiracil Hydrochloride, including repackagers and relabelers. The FDA regulates Tipiracil Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tipiracil Hydrochloride 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 Tipiracil Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Tipiracil Hydrochloride Suppliers

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

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

Tipiracil Hydrochloride USDMF

A Tipiracil Hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Tipiracil Hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Tipiracil Hydrochloride DMFs exist exist since differing nations have different regulations, such as Tipiracil Hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Tipiracil Hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Tipiracil Hydrochloride USDMF includes data on Tipiracil Hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tipiracil Hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Tipiracil Hydrochloride suppliers with USDMF on PharmaCompass.

Tipiracil Hydrochloride KDMF

In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.

Pharmaceutical companies submit a Tipiracil Hydrochloride Drug Master File in Korea (Tipiracil Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Tipiracil Hydrochloride. The MFDS reviews the Tipiracil Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Tipiracil Hydrochloride KDMF to evaluate the safety and efficacy of the drug.

After submitting a Tipiracil Hydrochloride KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Tipiracil Hydrochloride API can apply through the Korea Drug Master File (KDMF).

click here to find a list of Tipiracil Hydrochloride suppliers with KDMF on PharmaCompass.

Tipiracil Hydrochloride WC

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

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

Tipiracil Hydrochloride NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Tipiracil Hydrochloride as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Tipiracil Hydrochloride API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture Tipiracil Hydrochloride as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Tipiracil Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tipiracil Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Tipiracil Hydrochloride suppliers with NDC on PharmaCompass.

Tipiracil Hydrochloride GMP

Tipiracil Hydrochloride 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 Tipiracil Hydrochloride 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 Tipiracil Hydrochloride GMP manufacturer or Tipiracil Hydrochloride GMP API supplier for your needs.

Tipiracil Hydrochloride CoA

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

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

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