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1. Perhydrosqualene
1. 111-01-3
2. 2,6,10,15,19,23-hexamethyltetracosane
3. Perhydrosqualene
4. Dodecahydrosqualene
5. Cosbiol
6. Hexamethyltetracosane
7. Vitabiosol
8. Spinacane
9. Robane
10. Tetracosane, 2,6,10,15,19,23-hexamethyl-
11. Squalan
12. Nsc 6851
13. Squalane [nf]
14. Pripure 3759
15. Nsc-6851
16. Dermane
17. Gw89575kf9
18. Squalane (nf)
19. Ncgc00165976-01
20. Dsstox_cid_26513
21. Dsstox_rid_81682
22. Dsstox_gsid_46513
23. Hexamethyl Tetracosane
24. Caswell No. 482a
25. Cas-111-01-3
26. Einecs 203-825-6
27. Epa Pesticide Chemical Code 045503
28. Brn 0776019
29. Unii-gw89575kf9
30. Ai3-36494
31. Ccris 9473
32. Squalane N
33. Mfcd00008953
34. Squalane, 99%
35. Squalane [inci]
36. Squalane [ii]
37. Squalane [mi]
38. Squalane [vandf]
39. Squalane [mart.]
40. Squalane [usp-rs]
41. Squalane [who-dd]
42. Ec 203-825-6
43. Squalane, Analytical Standard
44. 4-01-00-00593 (beilstein Handbook Reference)
45. Squalane [ep Impurity]
46. Squalane [ep Monograph]
47. Chembl1552157
48. Dtxsid0046513
49. Nsc6851
50. Polysphere 3000 Sp (salt/mix)
51. Hy-n7113
52. Tox21_112277
53. S5407
54. Squalane, Technical, >=95% (gc)
55. Akos016012911
56. Tox21_112277_1
57. Ccg-268918
58. Cs-w014458
59. Db11420
60. Squalane 100 Microg/ml In Acetonitrile
61. 2,10,15,19,23-hexamethyltetracosane
62. Ncgc00165976-02
63. As-63438
64. Db-040948
65. Tetracosane,6,10,15,19,23-hexamethyl-
66. Ft-0631621
67. H0096
68. D05915
69. H12051
70. A894816
71. Q380055
72. Sr-01000944750
73. Sr-01000944750-1
74. W-109407
75. Squalane, European Pharmacopoeia (ep) Reference Standard
76. Squalane, United States Pharmacopeia (usp) Reference Standard
77. Squalane, Pharmaceutical Secondary Standard; Certified Reference Material
78. Dh7
79. Dodecahydrosqualene; Hexamethyltetracosane; Squalane; Tetracosane, 2,6,10,15,19,23-hexamethyl-, (all-e)-
| Molecular Weight | 422.8 g/mol |
|---|---|
| Molecular Formula | C30H62 |
| XLogP3 | 14.7 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 21 |
| Exact Mass | 422.485151978 g/mol |
| Monoisotopic Mass | 422.485151978 g/mol |
| Topological Polar Surface Area | 0 Ų |
| Heavy Atom Count | 30 |
| Formal Charge | 0 |
| Complexity | 308 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 4 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
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A Squalane manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Squalane, including repackagers and relabelers. The FDA regulates Squalane manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Squalane 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 Squalane manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Squalane supplier is an individual or a company that provides Squalane active pharmaceutical ingredient (API) or Squalane finished formulations upon request. The Squalane suppliers may include Squalane API manufacturers, exporters, distributors and traders.
click here to find a list of Squalane suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Squalane DMF (Drug Master File) is a document detailing the whole manufacturing process of Squalane active pharmaceutical ingredient (API) in detail. Different forms of Squalane DMFs exist exist since differing nations have different regulations, such as Squalane USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Squalane DMF submitted to regulatory agencies in the US is known as a USDMF. Squalane USDMF includes data on Squalane's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Squalane USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Squalane suppliers with USDMF on PharmaCompass.
Squalane 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 Squalane 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 Squalane GMP manufacturer or Squalane GMP API supplier for your needs.
A Squalane CoA (Certificate of Analysis) is a formal document that attests to Squalane's compliance with Squalane specifications and serves as a tool for batch-level quality control.
Squalane CoA mostly includes findings from lab analyses of a specific batch. For each Squalane 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.
Squalane may be tested according to a variety of international standards, such as European Pharmacopoeia (Squalane EP), Squalane JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Squalane USP).
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