Synopsis
Synopsis
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USDMF
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CEP/COS
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JDMF
0
EU WC
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KDMF
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NDC API
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VMF
0
EDQM
0
USP
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JP
0
Others
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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
DRUG PRODUCT COMPOSITIONS
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US Patents
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US Exclusivities
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Health Canada Patents
1. 16409-45-3
2. Menthol, Acetate
3. 89-48-5
4. Menthyl Acetate Racemic
5. Cyclohexanol, 5-methyl-2-(1-methylethyl)-, Acetate
6. 29066-34-0
7. (5-methyl-2-propan-2-ylcyclohexyl) Acetate
8. 2623-23-6
9. (+/-)-menthyl Acetate
10. 2230-87-7
11. 2-isopropyl-5-methylcyclohexyl Acetate
12. (+)-neomenthyl Acetate
13. D-neomenthyl Acetate
14. L-menthyl Acetate;(-)-menthyl Acetate
15. 5-methyl-2-(1-methylethyl)cyclohexanol Acetate
16. Neomenthol Acetate
17. Fema Number 2668
18. Hsdb 824
19. (.+/-.)-menthol Acetate
20. Einecs 240-459-6
21. Acetic Acid, P-menth-3-yl Ester, Dl-
22. Ai3-36197
23. Menthanyl Acetate
24. Cyclohexanol, 5-methyl-2-(1-methylethyl)-, Acetate, (1r,2r,5r)-rel-
25. Menthol, Neo-
26. Cyclohexanol, 5-methyl-2-(1-methylethyl)-, Acetate, (1.alpha.,2.beta.,5.alpha.)-
27. 20777-36-0
28. Einecs 218-767-7
29. (5r)-2-isopropyl-5-methylcyclohexyl Acetate
30. Starbld0011430
31. Menthyl Acetate, 97%
32. Menthylacetate97
33. (2-isopropyl-5-methyl-cyclohexyl) Acetate
34. Acetic Acid Menthyl Ester
35. Schembl57396
36. Chembl254585
37. 2-isopropyl-5-methylcyclohexyl Acetate, (1.alpha.,2.beta.,5.alpha.)-
38. Dtxsid20859153
39. Nsc7350
40. Acetic Acid, P-menth-3-yl Ester
41. Chebi:191550
42. (1s)-(+)-menthylacetate
43. Nsc-7350
44. Dl-menthyl Acetate, >=97%, Fg
45. Nsc122112
46. Akos015837885
47. Cis-1,3,trans-1,4- Menthol Acetate
48. Nsc 122112
49. Nsc-122112
50. Sb44841
51. Sb46743
52. As-83629
53. Db-063670
54. Db-071375
55. Ft-0604526
56. Ft-0604554
57. Ft-0628207
58. Ft-0631427
59. Ft-0690234
60. Ft-0694110
61. W-100373
62. Cyclohexanol, Acetate, (1.alpha.,2.alpha.,5.beta.)-
63. Menthyl Acetate, Primary Pharmaceutical Reference Standard
64. Cyclohexanol, Acetate, [1s-(1.alpha.,2.alpha.,5.beta.)]-
65. Cyclohexanol, 5-methyl-2-(1-methylethyl)-, Acetate, (1alpha,2alpha,5beta)-
66. Cyclohexanol, 5-methyl-2-(1-methylethyl)-, Acetate, (1.alpha.,2.beta.,5.alpha.)-(.+/-.)-
| Molecular Weight | 198.30 g/mol |
|---|---|
| Molecular Formula | C12H22O2 |
| XLogP3 | 3.6 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 3 |
| Exact Mass | 198.161979940 g/mol |
| Monoisotopic Mass | 198.161979940 g/mol |
| Topological Polar Surface Area | 26.3 Ų |
| Heavy Atom Count | 14 |
| Formal Charge | 0 |
| Complexity | 199 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 3 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
AS AN ESTER IT IS PRESUMABLY HYDROLYZED IN THE ALIMENTARY TRACT TO MENTHOL AND ACETIC ACID.
Gosselin, R.E., R.P. Smith, H.C. Hodge. Clinical Toxicology of Commercial Products. 5th ed. Baltimore: Williams and Wilkins, 1984., p. II-258
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ABOUT THIS PAGE
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PharmaCompass offers a list of Menthyl Acetate 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 Menthyl Acetate manufacturer or Menthyl Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Menthyl Acetate manufacturer or Menthyl Acetate supplier.
PharmaCompass also assists you with knowing the Menthyl Acetate API Price utilized in the formulation of products. Menthyl Acetate API Price is not always fixed or binding as the Menthyl Acetate Price is obtained through a variety of data sources. The Menthyl Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A (+)-Neomenthyl acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (+)-Neomenthyl acetate, including repackagers and relabelers. The FDA regulates (+)-Neomenthyl acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (+)-Neomenthyl acetate 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 (+)-Neomenthyl acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A (+)-Neomenthyl acetate supplier is an individual or a company that provides (+)-Neomenthyl acetate active pharmaceutical ingredient (API) or (+)-Neomenthyl acetate finished formulations upon request. The (+)-Neomenthyl acetate suppliers may include (+)-Neomenthyl acetate API manufacturers, exporters, distributors and traders.
click here to find a list of (+)-Neomenthyl acetate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
(+)-Neomenthyl acetate 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 (+)-Neomenthyl acetate 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 (+)-Neomenthyl acetate GMP manufacturer or (+)-Neomenthyl acetate GMP API supplier for your needs.
A (+)-Neomenthyl acetate CoA (Certificate of Analysis) is a formal document that attests to (+)-Neomenthyl acetate's compliance with (+)-Neomenthyl acetate specifications and serves as a tool for batch-level quality control.
(+)-Neomenthyl acetate CoA mostly includes findings from lab analyses of a specific batch. For each (+)-Neomenthyl acetate 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.
(+)-Neomenthyl acetate may be tested according to a variety of international standards, such as European Pharmacopoeia ((+)-Neomenthyl acetate EP), (+)-Neomenthyl acetate JP (Japanese Pharmacopeia) and the US Pharmacopoeia ((+)-Neomenthyl acetate USP).
