Synopsis
Synopsis
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CEP/COS
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JDMF
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KDMF
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NDC API
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USP
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JP
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Europe
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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
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PharmaCompass offers a list of MALOTILATE API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right MALOTILATE manufacturer or MALOTILATE supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred MALOTILATE manufacturer or MALOTILATE supplier.
PharmaCompass also assists you with knowing the MALOTILATE API Price utilized in the formulation of products. MALOTILATE API Price is not always fixed or binding as the MALOTILATE Price is obtained through a variety of data sources. The MALOTILATE Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DA-3857 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DA-3857, including repackagers and relabelers. The FDA regulates DA-3857 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DA-3857 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 DA-3857 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DA-3857 supplier is an individual or a company that provides DA-3857 active pharmaceutical ingredient (API) or DA-3857 finished formulations upon request. The DA-3857 suppliers may include DA-3857 API manufacturers, exporters, distributors and traders.
click here to find a list of DA-3857 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DA-3857 DMF (Drug Master File) is a document detailing the whole manufacturing process of DA-3857 active pharmaceutical ingredient (API) in detail. Different forms of DA-3857 DMFs exist exist since differing nations have different regulations, such as DA-3857 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A DA-3857 DMF submitted to regulatory agencies in the US is known as a USDMF. DA-3857 USDMF includes data on DA-3857's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The DA-3857 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of DA-3857 suppliers with USDMF on PharmaCompass.
DA-3857 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 DA-3857 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 DA-3857 GMP manufacturer or DA-3857 GMP API supplier for your needs.
A DA-3857 CoA (Certificate of Analysis) is a formal document that attests to DA-3857's compliance with DA-3857 specifications and serves as a tool for batch-level quality control.
DA-3857 CoA mostly includes findings from lab analyses of a specific batch. For each DA-3857 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.
DA-3857 may be tested according to a variety of international standards, such as European Pharmacopoeia (DA-3857 EP), DA-3857 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (DA-3857 USP).
