Synopsis
Synopsis
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CEP/COS
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JDMF
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NDC API
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API
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FDF
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FDF Dossiers
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FDA Orange Book
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Europe
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USP
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1. 1-octadecanamine, Hydrochloride
2. 1-octadecanamine, Hydrochloride (1:1)
3. 1-octadecylamine
4. Octadecyl Ammonium Chloride
5. Octadecylamine Hydrochloride
6. Stearamine
7. Stearyl Amine
8. Stearylamine
9. Stearylamine Hydrochloride
10. Stearylammonium Chloride
1. Octadecan-1-amine
2. 124-30-1
3. 1-octadecanamine
4. Octadecanamine
5. Stearamine
6. Stearylamine
7. 1-aminooctadecane
8. 1-octadecylamine
9. N-octadecylamine
10. Stearyl Amine
11. N-stearylamine
12. Armofilm
13. Armeen 18d
14. Monooctadecylamine
15. Nissan Amine Ab
16. Armeen 118d
17. Alamine 7
18. Noram Sh
19. Alamine 7d
20. Oktadecylamin
21. Adogenen 142
22. Armeen 18
23. Amine Ab
24. Farmin 80
25. Crodamine 1.18d
26. Hydrogenated Tallowamine
27. Kemamine P990
28. 61788-45-2
29. Kemamine P 990
30. Amines, Hydrogenated Tallow Alkyl
31. Nsc 9857
32. Armid Htd
33. Armeen 1180
34. Ffv58uny7o
35. Tallow Amine, Hydrogenated
36. Octadecane,1-amino
37. Octadecylamineadogenen 142
38. Chembl55860
39. Chebi:63866
40. Nsc-9857
41. Oktadecylamin [czech]
42. Octadecyl Amine
43. Ccris 4688
44. Hsdb 1194
45. Hydrogenated Tallow Amine
46. Einecs 204-695-3
47. Unii-ffv58uny7o
48. Brn 0636111
49. Ai3-14661
50. Steamfilm Fg
51. 1-octadecyl Amine
52. Einecs 262-976-6
53. Octadecylamine, 97%
54. 1-octadecanamine, 9ci
55. Stearamine [inci]
56. Amine 18-90
57. Ec 204-695-3
58. Ec 262-976-6
59. Nciopen2_007744
60. Schembl12291
61. Octadecylamine [hsdb]
62. 4-04-00-00825 (beilstein Handbook Reference)
63. Schembl2159903
64. Schembl3868686
65. Schembl6253291
66. Wln: Z18
67. Dtxsid1025801
68. Kemamine P-990, P-990d
69. Nsc9857
70. Octadecylamine, >=99.0% (gc)
71. Str09001
72. Bdbm50147579
73. Mfcd00008159
74. Stk062786
75. Zinc38141453
76. Akos000269090
77. Octadecylamine, Technical Grade, 90%
78. Cs-w012394
79. Ncgc00164134-01
80. Ft-0608174
81. Ft-0659903
82. O0014
83. D70506
84. A833419
85. J-005064
86. Q2013790
87. F3145-0795
Molecular Weight | 269.5 g/mol |
---|---|
Molecular Formula | C18H39N |
XLogP3 | 8.5 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 1 |
Rotatable Bond Count | 16 |
Exact Mass | 269.308250248 g/mol |
Monoisotopic Mass | 269.308250248 g/mol |
Topological Polar Surface Area | 26 Ų |
Heavy Atom Count | 19 |
Formal Charge | 0 |
Complexity | 145 |
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 |
API Imports and Exports
Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
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ABOUT THIS PAGE
A Stearylamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Stearylamine, including repackagers and relabelers. The FDA regulates Stearylamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Stearylamine API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Stearylamine supplier is an individual or a company that provides Stearylamine active pharmaceutical ingredient (API) or Stearylamine finished formulations upon request. The Stearylamine suppliers may include Stearylamine API manufacturers, exporters, distributors and traders.
click here to find a list of Stearylamine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Stearylamine DMF (Drug Master File) is a document detailing the whole manufacturing process of Stearylamine active pharmaceutical ingredient (API) in detail. Different forms of Stearylamine DMFs exist exist since differing nations have different regulations, such as Stearylamine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Stearylamine DMF submitted to regulatory agencies in the US is known as a USDMF. Stearylamine USDMF includes data on Stearylamine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Stearylamine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Stearylamine suppliers with USDMF on PharmaCompass.
Stearylamine 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 Stearylamine 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 Stearylamine GMP manufacturer or Stearylamine GMP API supplier for your needs.
A Stearylamine CoA (Certificate of Analysis) is a formal document that attests to Stearylamine's compliance with Stearylamine specifications and serves as a tool for batch-level quality control.
Stearylamine CoA mostly includes findings from lab analyses of a specific batch. For each Stearylamine 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.
Stearylamine may be tested according to a variety of international standards, such as European Pharmacopoeia (Stearylamine EP), Stearylamine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Stearylamine USP).
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