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1. Calcia
2. Calxyl
3. Heavy Calcium Oxide
4. Hexocalex
5. Hexocalex 6-9
6. Lime
7. Quicklime
1. 1305-78-8
2. Burnt Lime
3. Oxocalcium
4. Gebrannter Kalk
5. Calcium Monoxide
6. Calx
7. Calcium Oxide (cao)
8. Lime [usp]
9. Calcia
10. Calxyl
11. Chebi:31344
12. Mfcd00010911
13. Lime (usp)
14. Airlock
15. Chaux Vive
16. Quick Lime
17. Calx Usta
18. Rhenosorb C
19. Rhenosorb F
20. Desical P
21. Lime, Burned
22. Caloxal Cpa
23. Caloxol W3
24. Vesta Pp
25. Caloxol Cp2
26. Calcia (cao)
27. Bell Cml(e)
28. Bell Cml(p)
29. Caswell No. 147a
30. Wapniowy Tlenek
31. Qc-x
32. Wapniowy Tlenek [polish]
33. Oxyde De Calcium
34. Oxyde De Calcium [french]
35. Ccris 7496
36. Cml 21
37. Cml 31
38. Cml 35
39. Hsdb 1615
40. Einecs 215-138-9
41. Unii-c7x2m0vvnh
42. Un1910
43. Epa Pesticide Chemical Code 075604
44. Branntkalk
45. Kalziumoxid
46. Aetzkalk
47. Calciumoxide&nb
48. Caustic Lime
49. Lime Whole
50. Key Lime Whole
51. Calcium Oxide, Cp
52. Calcium Oxide, 98%
53. Calcium Oxide Dispersion
54. Calcium Oxide Nanopowder
55. Calcium Oxide (jp17)
56. Citrus Aurantiifolia Whole
57. Ec 215-138-9
58. Calcium Oxide, Reagent Grade
59. Tin(iv) Selenide (snse2)
60. Chembl2104397
61. Calcium Oxide, P.a., 95.0%
62. Akos015903966
63. Lime, Meets Usp Testing Specifications
64. Calcium Oxide, Vetec(tm) Reagent Grade
65. Calcium Oxide [un1910] [corrosive]
66. Calcium Oxide Nanoparticles / Nanopowder
67. Calcium Oxide, 99.995% Trace Metals Basis
68. Calcium Oxide, Saj First Grade, >=98.0%
69. Ft-0623408
70. Calcium Oxide, Saj Special Grade, >=98.0%
71. D01679
72. Q185006
73. J-005832
74. Calcium Oxide, Reagentplus(r), 99.9% Trace Metals Basis
75. Calcium Oxide, Anhydrous, Powder, >=99.99% Trace Metals Basis
76. Calcium Oxide, Nanopowder, <160 Nm Particle Size (bet), 98%
77. Calcium Oxide, 99.998% (metals Basis, Excluding Other Alkaline Earth And Alkali Metals 130 Ppm Max)
78. Calcium Oxide, Puriss., Meets Analytical Specification Of Fcc, 96-100.5% (ex Ignited Substance), Powder (fine)
| Molecular Weight | 56.08 g/mol |
|---|---|
| Molecular Formula | CaO |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Exact Mass | 55.9575055 g/mol |
| Monoisotopic Mass | 55.9575055 g/mol |
| Topological Polar Surface Area | 17.1 Ų |
| Heavy Atom Count | 2 |
| Formal Charge | 0 |
| Complexity | 2 |
| 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 |
Dental Materials
Materials used in the production of dental bases, restorations, impressions, prostheses, etc. (See all compounds classified as Dental Materials.)
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ABOUT THIS PAGE
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PharmaCompass offers a list of lime 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 lime manufacturer or lime supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred lime manufacturer or lime supplier.
PharmaCompass also assists you with knowing the lime API Price utilized in the formulation of products. lime API Price is not always fixed or binding as the lime Price is obtained through a variety of data sources. The lime Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Vesta PP manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vesta PP, including repackagers and relabelers. The FDA regulates Vesta PP manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vesta PP 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 Vesta PP supplier is an individual or a company that provides Vesta PP active pharmaceutical ingredient (API) or Vesta PP finished formulations upon request. The Vesta PP suppliers may include Vesta PP API manufacturers, exporters, distributors and traders.
click here to find a list of Vesta PP suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Vesta PP DMF (Drug Master File) is a document detailing the whole manufacturing process of Vesta PP active pharmaceutical ingredient (API) in detail. Different forms of Vesta PP DMFs exist exist since differing nations have different regulations, such as Vesta PP USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Vesta PP DMF submitted to regulatory agencies in the US is known as a USDMF. Vesta PP USDMF includes data on Vesta PP's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Vesta PP USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Vesta PP suppliers with USDMF on PharmaCompass.
Vesta PP 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 Vesta PP 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 Vesta PP GMP manufacturer or Vesta PP GMP API supplier for your needs.
A Vesta PP CoA (Certificate of Analysis) is a formal document that attests to Vesta PP's compliance with Vesta PP specifications and serves as a tool for batch-level quality control.
Vesta PP CoA mostly includes findings from lab analyses of a specific batch. For each Vesta PP 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.
Vesta PP may be tested according to a variety of international standards, such as European Pharmacopoeia (Vesta PP EP), Vesta PP JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Vesta PP USP).
