Synopsis
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1. 3-(2-aminoethyl)indole
2. Tryptamine Monohydrochloride
3. Tryptamine Sulfate
1. 61-54-1
2. 2-(1h-indol-3-yl)ethanamine
3. 3-(2-aminoethyl)indole
4. 1h-indole-3-ethanamine
5. 2-(3-indolyl)ethylamine
6. Indol-3-ethylamine
7. Tryptamin
8. Indole, 3-(2-aminoethyl)-
9. 2-(indol-3-yl)ethylamine
10. 2-(1h-indol-3-yl)ethan-1-amine
11. 2-(1h-indol-3-yl)ethylamine
12. 3-indoleethylamine
13. 2-indol-3-ylethylamine
14. 2-(1h-indol-3-yl)-ethylamine
15. 3-indoleethanamine
16. (amino-2 Ethyl)-3 Indole
17. Mfcd00005661
18. (amino-2 Ethyl)-3 Indole [french]
19. Brn 0125513
20. Chembl6640
21. .beta.-(3-indolyl)ethylamine
22. 3-(2-aminoethyl)-1h-indole
23. 422zu9n5tv
24. Chebi:16765
25. Tryptamine, Free Base
26. 3-[2-aminoethyl]indole
27. Nsc-165212
28. Einecs 200-510-5
29. Beta-(3-indolyl)ethylamine
30. Triptamine
31. Unii-422zu9n5tv
32. Ccris 8959
33. Sr-01000075589
34. 3-indolylethylamine
35. Tsh
36. Tryptamine, 98%
37. (3-indolyl)ethylamine
38. Spectrum_000033
39. Tryptamine [mi]
40. Spectrum2_000873
41. Spectrum3_001890
42. Spectrum4_000850
43. Spectrum5_001296
44. 2-indol-3-yl-ethylamine
45. 2-indol-3-yl-aethylamin
46. 3-(2-amino)ethyl Indole
47. Bmse000207
48. Ec 200-510-5
49. Lopac-246557
50. 3-(beta-aminoethyl)-indole
51. Lopac0_000061
52. Oprea1_870097
53. Schembl26725
54. Bspbio_003400
55. Gtpl125
56. Kbiogr_001459
57. Kbioss_000393
58. 5-22-10-00045 (beilstein Handbook Reference)
59. Mls000515794
60. Divk1c_000862
61. Spectrum1503922
62. Spbio_000945
63. Tryptamine, Analytical Standard
64. Dtxsid2075340
65. Schembl13006684
66. 2-(1h-indol-3-yl) Ethylamine
67. Hms502l04
68. Kbio1_000862
69. Kbio2_000393
70. Kbio2_002961
71. Kbio2_005529
72. Kbio3_002903
73. Ninds_000862
74. 2-(1h-indol-3-yl)-ethyl-amine
75. Hms1922k18
76. Hms2267b18
77. Hms3885e17
78. Zinc120144
79. 2-(1h-indol-3-yl)ethanamine #
80. Act09907
81. Albb-017957
82. Bcp21605
83. Cs-d1750
84. Hy-b2132
85. Bbl015353
86. Bdbm50024210
87. Ccg-40088
88. S3627
89. Stk262895
90. Akos000119468
91. Db08653
92. Fs-3317
93. Sdccgmls-0066798.p001
94. Sdccgsbi-0050049.p003
95. Idi1_000862
96. Ncgc00014994-01
97. Ncgc00014994-02
98. Ncgc00014994-03
99. Ncgc00014994-04
100. Ncgc00014994-05
101. Ncgc00014994-06
102. Ncgc00014994-07
103. Ncgc00014994-11
104. Ncgc00095081-01
105. Ncgc00095081-02
106. Ncgc00095081-03
107. Ncgc00095081-04
108. Ncgc00095081-05
109. Am807158
110. Bp-12561
111. Smr000112268
112. Sy001383
113. Db-005731
114. Tryptamine, Vetec(tm) Reagent Grade, 98%
115. Ft-0613523
116. T0890
117. (amino-2 Ethyl)-3 Indole;3-indoleethylamine
118. C00398
119. T-8095
120. T-8100
121. 005t661
122. Ae-848/30735051
123. L000946
124. Q409439
125. Sr-01000075589-5
126. Brd-k44218819-001-05-1
127. F2169-0960
128. 5e7b376b-5933-446c-9d88-661b5f480122
| Molecular Weight | 160.22 g/mol |
|---|---|
| Molecular Formula | C10H12N2 |
| XLogP3 | 1.6 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 2 |
| Exact Mass | 160.100048391 g/mol |
| Monoisotopic Mass | 160.100048391 g/mol |
| Topological Polar Surface Area | 41.8 Ų |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 147 |
| 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 |
Drugs in Development
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PharmaCompass offers a list of Tryptamine 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 Tryptamine manufacturer or Tryptamine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tryptamine manufacturer or Tryptamine supplier.
PharmaCompass also assists you with knowing the Tryptamine API Price utilized in the formulation of products. Tryptamine API Price is not always fixed or binding as the Tryptamine Price is obtained through a variety of data sources. The Tryptamine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tryptamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tryptamine, including repackagers and relabelers. The FDA regulates Tryptamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tryptamine 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 Tryptamine supplier is an individual or a company that provides Tryptamine active pharmaceutical ingredient (API) or Tryptamine finished formulations upon request. The Tryptamine suppliers may include Tryptamine API manufacturers, exporters, distributors and traders.
Tryptamine 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 Tryptamine 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 Tryptamine GMP manufacturer or Tryptamine GMP API supplier for your needs.
A Tryptamine CoA (Certificate of Analysis) is a formal document that attests to Tryptamine's compliance with Tryptamine specifications and serves as a tool for batch-level quality control.
Tryptamine CoA mostly includes findings from lab analyses of a specific batch. For each Tryptamine 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.
Tryptamine may be tested according to a variety of international standards, such as European Pharmacopoeia (Tryptamine EP), Tryptamine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Tryptamine USP).
