Synopsis
Synopsis
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USDMF
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CEP/COS
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JDMF
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EU WC
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KDMF
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NDC API
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VMF
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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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Canada
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Australia
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South Africa
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Listed Dossiers
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USP
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JP
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1. Guanidinium Thiocyanate
2. Guscn
1. 593-84-0
2. Guanidinium Thiocyanate
3. Guanidinium Rhodanide
4. Guanidine;thiocyanic Acid
5. Guanidinium Isothiocyanate
6. Thiocyanic Acid, Compd. With Guanidine (1:1)
7. Mfcd00013027
8. Gca2eu297u
9. Nsc-2119
10. Gtc
11. Usaf Ek-705
12. Guanidinethiocyanate
13. Nsc 2119
14. Einecs 209-812-1
15. Buffer Avl
16. Ai3-18430
17. Unii-gca2eu297u
18. Schembl28942
19. Guanidine Thiocyanate Solu-tion
20. Guanidine Thiocyanate, Ultrapure
21. Dtxsid6060478
22. Isothiocyanic Acid, Compd. With Guanidine (1:1) (van)
23. Nsc2119
24. Guanidine Thiocyanate, >=99.5%
25. Hy-d0841
26. Akos015961014
27. Guanidine Thiocyanate, >=97.0% (at)
28. Bp-13066
29. Ls-12942
30. Sy003172
31. Guanidine Thiocyanate, >=97% (titration)
32. Cs-0014812
33. G0230
34. G0360
35. Guanidine Thiocyanate, Molecular Biology Grade
36. G-8100
37. G-8102
38. M01833
39. Isothiocyanic Acid, Compd. With Guanidine (1:1)
40. Q904487
41. Guanidine Thiocyanate, For Molecular Biology, >=99%
42. Guanidine Thiocyanate, Vetec(tm) Reagent Grade, >=97%
43. Guanidine Thiocyanate, Bioreagent, For Molecular Biology, >=99%
44. Guanidine Thiocyanate, Bioultra, For Molecular Biology, >=99.0% (at)
45. Guanidine Thiocyanate Solution, Bioultra, For Molecular Biology, ~4 M In H2o
46. Guanidine Thiocyanate Solution, Bioultra, For Molecular Biology, ~6 M In H2o
| Molecular Weight | 118.16 g/mol |
|---|---|
| Molecular Formula | C2H6N4S |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 0 |
| Exact Mass | 118.03131738 g/mol |
| Monoisotopic Mass | 118.03131738 g/mol |
| Topological Polar Surface Area | 101 Ų |
| Heavy Atom Count | 7 |
| Formal Charge | 0 |
| Complexity | 57.6 |
| 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 |
Disinfectants
Substances used on inanimate objects that destroy harmful microorganisms or inhibit their activity. Disinfectants are classed as complete, destroying SPORES as well as vegetative forms of microorganisms, or incomplete, destroying only vegetative forms of the organisms. They are distinguished from ANTISEPTICS, which are local anti-infective agents used on humans and other animals. (From Hawley's Condensed Chemical Dictionary, 11th ed) (See all compounds classified as Disinfectants.)
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ABOUT THIS PAGE
A Guanidine Thiocyanate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Guanidine Thiocyanate, including repackagers and relabelers. The FDA regulates Guanidine Thiocyanate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Guanidine Thiocyanate 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 Guanidine Thiocyanate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Guanidine Thiocyanate supplier is an individual or a company that provides Guanidine Thiocyanate active pharmaceutical ingredient (API) or Guanidine Thiocyanate finished formulations upon request. The Guanidine Thiocyanate suppliers may include Guanidine Thiocyanate API manufacturers, exporters, distributors and traders.
click here to find a list of Guanidine Thiocyanate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Guanidine Thiocyanate 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 Guanidine Thiocyanate 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 Guanidine Thiocyanate GMP manufacturer or Guanidine Thiocyanate GMP API supplier for your needs.
A Guanidine Thiocyanate CoA (Certificate of Analysis) is a formal document that attests to Guanidine Thiocyanate's compliance with Guanidine Thiocyanate specifications and serves as a tool for batch-level quality control.
Guanidine Thiocyanate CoA mostly includes findings from lab analyses of a specific batch. For each Guanidine Thiocyanate 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.
Guanidine Thiocyanate may be tested according to a variety of international standards, such as European Pharmacopoeia (Guanidine Thiocyanate EP), Guanidine Thiocyanate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Guanidine Thiocyanate USP).
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