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1. 1,3-dimethylol-5,5-dimethylhydantoin
2. Dmdm Hydantoin
1. 6440-58-0
2. Dmdm Hydantoin
3. Dimethyloldimethyl Hydantoin
4. Dmdmh
5. Glydant
6. 1,3-bis(hydroxymethyl)-5,5-dimethylhydantoin
7. 1,3-dimethylol-5,5-dimethylhydantoin
8. Dimethylol-5,5-dimethylhydantoin
9. Dimethyloldimethylhydantoin
10. 2,4-imidazolidinedione, 1,3-bis(hydroxymethyl)-5,5-dimethyl-
11. 1,3-bis(hydroxymethyl)-5,5-dimethyl-2,4-imidazolidinedione
12. Byr0546tow
13. 1,3-dihydroxymethyl-5,5-dimethylhydantoin
14. Mfcd00467199
15. 1,3-dimethylol-5,5-dimethyl-hydantoin
16. Dantoin-dmdmh
17. Glycoserve-dmdmh
18. Dantoin Dmdmh 55
19. Dmdmh 55
20. Caswell No. 273ab
21. Einecs 229-222-8
22. Unii-byr0546tow
23. Epa Pesticide Chemical Code 115501
24. Brn 0882348
25. 1,3-di(hydroxymethyl)-5,5-dimethylhydantoin
26. Hsdb 7488
27. 1,3-dihydroxylmethyl-5,5-dimethylhydantoin
28. Ec 229-222-8
29. Dimethylol Dimethyl Hydantoin
30. Dmdm Hydantoin [ii]
31. Dsstox_cid_15217
32. Dsstox_gsid_35217
33. Schembl69185
34. Hydantoin, 1,3-bis(hydroxymethyl)-5,5-dimethyl-
35. Dmdm Hydantoin [inci]
36. Dmdm Hydantion [vandf]
37. Dmdm Hydantoin [vandf]
38. Dtxsid8035217
39. Zinc2033948
40. Tox21_303842
41. Akos006345746
42. Cs-w021276
43. Ncgc00356947-01
44. As-10924
45. Sy101650
46. Cas-6440-58-0
47. Ft-0606699
48. H11751
49. 440b580
50. A834743
51. Q5205613
52. W-104844
53. 1,3-dimethylol-5,5-dimethylhydantoin [hsdb]
54. 1,3-bis (hydroxymethyl)-5,5-dimethylimidazolidine-2,4-dione
55. 1,3 Bis(hydroxymethyl)-5,5- Dimethylhydantoindimethylhydantoin
56. 5-ethyl-1,3-dihydroxy-5-methyl-imidazolidine-2,4-dione;1,3-bis(hydroxymethyl)-5,5-dimethylimidazolidine-2,4-dione
Molecular Weight | 188.18 g/mol |
---|---|
Molecular Formula | C7H12N2O4 |
XLogP3 | -0.2 |
Hydrogen Bond Donor Count | 2 |
Hydrogen Bond Acceptor Count | 4 |
Rotatable Bond Count | 2 |
Exact Mass | 188.07970687 g/mol |
Monoisotopic Mass | 188.07970687 g/mol |
Topological Polar Surface Area | 81.1 Ų |
Heavy Atom Count | 13 |
Formal Charge | 0 |
Complexity | 251 |
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 |
A 0.1 mL aqueous solution containing 0.1 mCi of 1,3-dihydroxymethyl-5,5'-dimethylhydantoin-5-(14)-C was applied to the middorsal area of young adult male Sprague-Dawley rats. After 72 hours, more than 90% of the applied dose was recovered; more than 98% of the recovered activity was confined to the dose site. At the time of killing, less than 1% of the radioactivity was distributed in all body tissues. The higher counts of radioactivity were reported for the gastrointestinal tract, liver, and bone marrow. For most tissue samples, there was no evidence of accumulation of DMDM Hydantoin or its metabolites. DMDM Hydantoin and its metabolites are excreted primarily via the urine. The amount of (14)C activity in the urine decreased approximately 6 times over a 72-hour period; radioactivity in the feces remained approximately constant and significantly below that of the urine.
Cosmetic Ingredient Review Panel; Final Report on the Safety Assessment of DMDM Hydantoin. J Am Coll Toxicol 7 (3): 245-77 (1988)
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A Glydant manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glydant, including repackagers and relabelers. The FDA regulates Glydant manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glydant 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 Glydant supplier is an individual or a company that provides Glydant active pharmaceutical ingredient (API) or Glydant finished formulations upon request. The Glydant suppliers may include Glydant API manufacturers, exporters, distributors and traders.
Glydant 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 Glydant 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 Glydant GMP manufacturer or Glydant GMP API supplier for your needs.
A Glydant CoA (Certificate of Analysis) is a formal document that attests to Glydant's compliance with Glydant specifications and serves as a tool for batch-level quality control.
Glydant CoA mostly includes findings from lab analyses of a specific batch. For each Glydant 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.
Glydant may be tested according to a variety of international standards, such as European Pharmacopoeia (Glydant EP), Glydant JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Glydant USP).