Synopsis
Synopsis
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FDA Orange Book
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1. 2-phenethylamine
2. 2-phenylethylamine
3. 2-phenylethylammonium Chloride
4. Beta-phenethylamine
5. Beta-phenylethylamine
6. Diphenethylamine Sulfate
7. Phenethylamine
8. Phenethylamine Conjugate Acid
9. Phenethylamine Hydrobromide
10. Phenethylamine Hydrochloride
11. Phenethylamine Mesylate
12. Phenethylamine Perchlorate
13. Phenethylamine Sulfate
14. Phenethylamine Sulfate (2:1)
15. Phenethylamine Tosylate
16. Phenethylamine, 15n-labeled Cpd
17. Phenethylamine, Beta-(14)c-labeled Cpd
18. Phenethylamine, Monolithium Salt
1. 156-28-5
2. 2-phenylethanamine Hydrochloride
3. Phenethylamine Hydrochloride
4. Benzeneethanamine, Hydrochloride
5. Phenethylammonium Chloride
6. Benzeneethanamine, Hydrochloride (1:1)
7. Usaf El-76
8. Benzeneethanamine Hydrochloride
9. 1-phenyl-2-aminoethane Hydrochloride
10. 2-phenylethylamine (hydrochloride)
11. Phenylethylamine Hydrochloride
12. 2-phenylethan-1-amine Hydrochloride
13. Vof61xw69d
14. 2-phenylethanamine;hydrochloride
15. .beta.-phenethylamine Hydrochloride
16. .beta.-phenylethylamine Hydrochloride
17. Nsc-138569
18. Beta-phenethylamine Hydrochloride
19. Beta-phenylethylamine Hydrochloride
20. .beta.-phenylathylaminhydrochlorid
21. Beta-phenylathylaminhydrochlorid
22. 2-phenylethylamine Hcl
23. Einecs 205-849-2
24. Unii-vof61xw69d
25. Nsc 138569
26. Beta-phenylathylaminhydrochlorid [german]
27. Mfcd00012893
28. Phenethylamine Hcl
29. Benzylmethylammonium Chloride
30. Schembl245154
31. Wln: Z2r & Gh
32. B-phenylethylamine Hydrochloride
33. B-aminoethylbenzene Hydrochloride
34. Dtxsid0059744
35. Hy-w010483a
36. Nsc138569
37. S5346
38. Akos004905243
39. Ccg-214630
40. Gs-3011
41. Phenethylamine Hydrochloride [mi]
42. 2-phenylethylamine Hydrochloride, >=98%
43. Db-043308
44. 1-amino-2-phenylethane Hydrochloride
45. Cs-0083209
46. Ft-0631856
47. P0086
48. Phenethylamine Hydrochloride [who-dd]
49. P-3700
50. Q27291936
51. 2-phenylethylamine Hydrochloride (phenethylamine Hydrochloride; Pea Hcl)
52. 2-phenylethylamine Hydrochloride, Certified Reference Material, Tracecert(r)
53. 2-phenylethylamine Hydrochloride (phenethylamine Hydrochloride; Pea Hcl) 1.0 Mg/ml In Methanol (as Free Base)
Molecular Weight | 157.64 g/mol |
---|---|
Molecular Formula | C8H12ClN |
Hydrogen Bond Donor Count | 2 |
Hydrogen Bond Acceptor Count | 1 |
Rotatable Bond Count | 2 |
Exact Mass | 157.0658271 g/mol |
Monoisotopic Mass | 157.0658271 g/mol |
Topological Polar Surface Area | 26 Ų |
Heavy Atom Count | 10 |
Formal Charge | 0 |
Complexity | 65 |
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 | 2 |
Psychotropic Drugs
A loosely defined grouping of drugs that have effects on psychological function. Here the psychotropic agents include the antidepressive agents, hallucinogens, and tranquilizing agents (including the antipsychotics and anti-anxiety agents). (See all compounds classified as Psychotropic Drugs.)
API Imports and Exports
Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
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ABOUT THIS PAGE
A Phenethylamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Phenethylamine, including repackagers and relabelers. The FDA regulates Phenethylamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Phenethylamine 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 Phenethylamine supplier is an individual or a company that provides Phenethylamine active pharmaceutical ingredient (API) or Phenethylamine finished formulations upon request. The Phenethylamine suppliers may include Phenethylamine API manufacturers, exporters, distributors and traders.
click here to find a list of Phenethylamine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Phenethylamine DMF (Drug Master File) is a document detailing the whole manufacturing process of Phenethylamine active pharmaceutical ingredient (API) in detail. Different forms of Phenethylamine DMFs exist exist since differing nations have different regulations, such as Phenethylamine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Phenethylamine DMF submitted to regulatory agencies in the US is known as a USDMF. Phenethylamine USDMF includes data on Phenethylamine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Phenethylamine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Phenethylamine suppliers with USDMF on PharmaCompass.
Phenethylamine 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 Phenethylamine 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 Phenethylamine GMP manufacturer or Phenethylamine GMP API supplier for your needs.
A Phenethylamine CoA (Certificate of Analysis) is a formal document that attests to Phenethylamine's compliance with Phenethylamine specifications and serves as a tool for batch-level quality control.
Phenethylamine CoA mostly includes findings from lab analyses of a specific batch. For each Phenethylamine 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.
Phenethylamine may be tested according to a variety of international standards, such as European Pharmacopoeia (Phenethylamine EP), Phenethylamine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Phenethylamine USP).
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