Synopsis
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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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FDA Orange Book
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Europe
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Canada
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Australia
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South Africa
DRUG PRODUCT COMPOSITIONS
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US Patents
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US Exclusivities
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Health Canada Patents
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Stock Recap #PipelineProspector
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US Medicaid
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1. Beta-maltose
2. 69-79-4
3. 133-99-3
4. D-maltose
5. Maltobiose
6. D-(+)-maltose
7. 4-o-alpha-d-glucopyranosyl-beta-d-glucopyranose
8. Cextromaltose
9. Finetose
10. Maltodiose
11. Sunmalt
12. Malt Sugar
13. Finetose F
14. Sunmalt S
15. Cellobiose
16. R4b6462ngr
17. Insulin, (arg-insulin)
18. Maltose, Pure
19. Chebi:18147
20. Beta-d-cellobiose
21. Beta-d-glucopyranose, 4-o-alpha-d-glucopyranosyl-
22. 4-o-alpha-d-glucopyranosyl-d-glucose
23. Nsc-760396
24. (2r,3s,4s,5r,6r)-2-(hydroxymethyl)-6-[(2r,3s,4r,5r,6r)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol
25. 120022-04-0
26. Beta-d-glucopyranosyl(1-4)-d-glucopyranose
27. 4-(alpha-d-glucosido)-d-glucose
28. 4-(alpha-d-glucopyranosido)-alpha-glucopyranose
29. D-glucose, 4-o-alpha-d-glucopyranosyl-
30. B-d-glucopyranose, 4-o-a-d-glucopyranosyl-
31. Alpha-d-glucopyranosyl-(1->4)-beta-d-glucopyranose
32. Ai3-09089
33. Maltose Anhydrous
34. Maltose Hh
35. Maltose Hhh
36. Advantose 100
37. Beta-d-maltose
38. Maltose, Beta-
39. (2r,3r,4r,5r)-2,3,5,6-tetrahydroxy-4-(((2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2h-pyran-2-yl)oxy)hexanal
40. Maltose Beta-anomer
41. Unii-r4b6462ngr
42. Maltroise
43. 1wdr
44. N9s
45. Glca1-4glcb
46. Glcalpha1-4glcbeta
47. Maltose (8ci)
48. Sunmalt-s
49. 2f5t
50. .beta.-maltose
51. Maltose, Unspecified Form
52. .beta.-d-maltose
53. .beta.-d-cellobiose
54. Schembl15064
55. Maltose .beta.-anomer
56. .beta.-d-glucopyranose, 4-o-.alpha.-d-glucopyranosyl-
57. Chembl1908365
58. Dtxsid901318570
59. Hms3264c14
60. Pharmakon1600-01301024
61. Zinc4095762
62. Mfcd00079443
63. Nsc760396
64. Alpha-d-glcp-(1->4)-beta-d-glcp
65. Ccg-231520
66. Ncgc00389762-01
67. Bs-10031
68. C01971
69. D70315
70. 4-o-(alpha-d-glucopyranosyl)-beta-d-glucopyranose
71. Alpha-d-glucopyranose-(1->4)-beta-d-glucopyranose
72. 857a38d2-86d7-41f1-bc3c-dadbc19cf9dc
73. D-glucose, 4-o-alpha-d-glucopyranosyl- (6ci,9ci)
74. Q26914030
75. Wurcs=2.0/2,2,1/[a2122h-1b_1-5][a2122h-1a_1-5]/1-2/a4-b1
76. (2r,3s,4s,5r,6r)-2-methylol-6-[(2r,3s,4r,5r,6r)-4,5,6-trihydroxy-2-methylol-tetrahydropyran-3-yl]oxy-tetrahydropyran-3,4,5-triol
| Molecular Weight | 342.30 g/mol |
|---|---|
| Molecular Formula | C12H22O11 |
| XLogP3 | -4.7 |
| Hydrogen Bond Donor Count | 8 |
| Hydrogen Bond Acceptor Count | 11 |
| Rotatable Bond Count | 4 |
| Exact Mass | 342.11621151 g/mol |
| Monoisotopic Mass | 342.11621151 g/mol |
| Topological Polar Surface Area | 190 Ų |
| Heavy Atom Count | 23 |
| Formal Charge | 0 |
| Complexity | 382 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 10 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
Sweetening Agents
Substances that sweeten food, beverages, medications, etc., such as sugar, saccharine or other low-calorie synthetic products. (From Random House Unabridged Dictionary, 2d ed) (See all compounds classified as Sweetening Agents.)
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A Maltose manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Maltose, including repackagers and relabelers. The FDA regulates Maltose manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Maltose 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 Maltose manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Maltose supplier is an individual or a company that provides Maltose active pharmaceutical ingredient (API) or Maltose finished formulations upon request. The Maltose suppliers may include Maltose API manufacturers, exporters, distributors and traders.
click here to find a list of Maltose suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Maltose DMF (Drug Master File) is a document detailing the whole manufacturing process of Maltose active pharmaceutical ingredient (API) in detail. Different forms of Maltose DMFs exist exist since differing nations have different regulations, such as Maltose USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Maltose DMF submitted to regulatory agencies in the US is known as a USDMF. Maltose USDMF includes data on Maltose's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Maltose USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Maltose suppliers with USDMF on PharmaCompass.
Maltose 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 Maltose 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 Maltose GMP manufacturer or Maltose GMP API supplier for your needs.
A Maltose CoA (Certificate of Analysis) is a formal document that attests to Maltose's compliance with Maltose specifications and serves as a tool for batch-level quality control.
Maltose CoA mostly includes findings from lab analyses of a specific batch. For each Maltose 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.
Maltose may be tested according to a variety of international standards, such as European Pharmacopoeia (Maltose EP), Maltose JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Maltose USP).
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