Synopsis
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1. Diisopropyl 1,3-dithiol-2-ylidenemalonate
2. Nkk 105
3. Nkk-105
1. 59937-28-9
2. Kantec
3. Nkk 105
4. Malotilatum
5. Nkk-105
6. Diisopropyl 1,3-dithiol-2-ylidenemalonate
7. Dipropan-2-yl 2-(1,3-dithiol-2-ylidene)propanedioate
8. Hepation
9. Diisopropyl 2-(1,3-dithiol-2-ylidene)malonate
10. 1,3-dithiol-2-ylidenepropanedioic Acid, Bis(1-methylethyl) Ester
11. Rv59pnd975
12. Propanedioic Acid, 1,3-dithiol-2-ylidene-, Bis(1-methylethyl) Ester
13. Ncgc00164588-01
14. Dsstox_cid_26463
15. Dsstox_rid_81637
16. Dsstox_gsid_46463
17. Malotilato
18. 1,3-bis(propan-2-yl) 2-(2h-1,3-dithiol-2-ylidene)propanedioate
19. Malotilatum [inn-latin]
20. Malotilato [inn-spanish]
21. Malotilate [usan:inn:jan]
22. Cas-59937-28-9
23. Einecs 261-987-3
24. Cl-1500
25. Unii-rv59pnd975
26. Tractal
27. Diisopropyl-1,3-dithiol-2-ylidenemalonate
28. Malotilate- Bio-x
29. Kantec (tn)
30. Diisopropyl 1,3-dithiole-delta(sup 2,alpha)-malonate
31. Malotilate [mi]
32. Malotilate [inn]
33. Malotilate [jan]
34. Malotilate [usan]
35. Malotilate [mart.]
36. Malotilate [who-dd]
37. Mls006010037
38. Malotilate (jan/usan/inn)
39. Schembl635496
40. Chembl1697754
41. Dtxsid7046463
42. Chebi:31798
43. Hms3654i08
44. Amy39997
45. Bcp01805
46. Hy-a0060
47. Zinc1542902
48. Tox21 112214
49. Tox21_112214
50. Malonic Acid, (1,3-dithiol-2-ylidene)-, Diisopropyl Ester
51. Mfcd00867646
52. S1137
53. Akos025119303
54. Tox21_112214_1
55. Bcp9000892
56. Ccg-267362
57. Cs-1594
58. Da-3857
59. Ncgc00164588-02
60. Ncgc00164588-03
61. As-11770
62. Bm164653
63. Smr002530051
64. Diisopropyl (1,3-dithiol-2-ylidene)malonate
65. Ft-0601567
66. M2674
67. Sw219173-1
68. D01770
69. F10956
70. Ab01566806_01
71. 937m289
72. A869087
73. Q6744548
74. Bis(1-methylethyl) 1,3-dithiol-2-ylidenepropanedioate
75. Brd-k97884852-001-02-1
76. (1,3-dithiol-2-ylidene)malonic Acid Diisopropyl Ester
77. Propanedioic Acid, 2-(1,3-dithiol-2-ylidene)-, 1,3-bis(1-methylethyl) Ester
| Molecular Weight | 288.4 g/mol |
|---|---|
| Molecular Formula | C12H16O4S2 |
| XLogP3 | 3.8 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 6 |
| Exact Mass | 288.04900133 g/mol |
| Monoisotopic Mass | 288.04900133 g/mol |
| Topological Polar Surface Area | 103 Ų |
| Heavy Atom Count | 18 |
| Formal Charge | 0 |
| Complexity | 363 |
| 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 |
ABOUT THIS PAGE
A MALOTILATE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MALOTILATE, including repackagers and relabelers. The FDA regulates MALOTILATE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MALOTILATE 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 MALOTILATE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A MALOTILATE supplier is an individual or a company that provides MALOTILATE active pharmaceutical ingredient (API) or MALOTILATE finished formulations upon request. The MALOTILATE suppliers may include MALOTILATE API manufacturers, exporters, distributors and traders.
click here to find a list of MALOTILATE suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A MALOTILATE DMF (Drug Master File) is a document detailing the whole manufacturing process of MALOTILATE active pharmaceutical ingredient (API) in detail. Different forms of MALOTILATE DMFs exist exist since differing nations have different regulations, such as MALOTILATE USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A MALOTILATE DMF submitted to regulatory agencies in the US is known as a USDMF. MALOTILATE USDMF includes data on MALOTILATE's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The MALOTILATE USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of MALOTILATE suppliers with USDMF on PharmaCompass.
MALOTILATE 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 MALOTILATE 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 MALOTILATE GMP manufacturer or MALOTILATE GMP API supplier for your needs.
A MALOTILATE CoA (Certificate of Analysis) is a formal document that attests to MALOTILATE's compliance with MALOTILATE specifications and serves as a tool for batch-level quality control.
MALOTILATE CoA mostly includes findings from lab analyses of a specific batch. For each MALOTILATE 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.
MALOTILATE may be tested according to a variety of international standards, such as European Pharmacopoeia (MALOTILATE EP), MALOTILATE JP (Japanese Pharmacopeia) and the US Pharmacopoeia (MALOTILATE USP).
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