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1. 4,5-dibromorhodamine Methyl Ester
2. Dibr-rh-me
1. 934qhk1ook
2. 1373958-68-9
3. Methyl 2-(3-amino-4,5-dibromo-6-iminoxanthen-9-yl)benzoate
4. Unii-934qhk1ook
5. Schembl2730919
6. 4,5 Dibromorhodamine Methyl Ester
7. 4,5-dibromorhodamine Methyl Ester
8. 4,5-dibromorhodamine 123 Free Base
9. Q27271555
10. Benzoic Acid, 2-(6-amino-4,5-dibromo-3-imino-3h-xanthen-9-yl)-, Methyl Ester
| Molecular Weight | 502.2 g/mol |
|---|---|
| Molecular Formula | C21H14Br2N2O3 |
| XLogP3 | 4.1 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 3 |
| Exact Mass | 501.93507 g/mol |
| Monoisotopic Mass | 499.93712 g/mol |
| Topological Polar Surface Area | 85.4 Ų |
| Heavy Atom Count | 28 |
| Formal Charge | 0 |
| Complexity | 789 |
| 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
A TH-9402 free base manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of TH-9402 free base, including repackagers and relabelers. The FDA regulates TH-9402 free base manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. TH-9402 free base 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 TH-9402 free base supplier is an individual or a company that provides TH-9402 free base active pharmaceutical ingredient (API) or TH-9402 free base finished formulations upon request. The TH-9402 free base suppliers may include TH-9402 free base API manufacturers, exporters, distributors and traders.
TH-9402 free base 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 TH-9402 free base 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 TH-9402 free base GMP manufacturer or TH-9402 free base GMP API supplier for your needs.
A TH-9402 free base CoA (Certificate of Analysis) is a formal document that attests to TH-9402 free base's compliance with TH-9402 free base specifications and serves as a tool for batch-level quality control.
TH-9402 free base CoA mostly includes findings from lab analyses of a specific batch. For each TH-9402 free base 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.
TH-9402 free base may be tested according to a variety of international standards, such as European Pharmacopoeia (TH-9402 free base EP), TH-9402 free base JP (Japanese Pharmacopeia) and the US Pharmacopoeia (TH-9402 free base USP).
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