1352008
USP
Isosorbide
United States Pharmacopeia (USP) Reference Standard
Synonym(s):
Dianhydro-D-glucitol solution
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About This Item
Empirical Formula (Hill Notation):
C6H10O4
Molecular Weight:
146.14
UNSPSC Code:
41116107
NACRES:
NA.24
grade
pharmaceutical primary standard
API family
isosorbide
manufacturer/tradename
USP
application(s)
pharmaceutical (small molecule)
format
neat
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General description
This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.
Application
Isosorbide USP reference standard, intended for use in specified quality tests and assays as specified in the USP compendia. Also, for use with USP monographs such as:
- Diluted Isosorbide Mononitrate
- Isosorbide Concentrate
- Isosorbide Mononitrate Extended-Release Tablets
- Isosorbide Mononitrate Tablets
- Isosorbide Oral Solution
- Sorbitan Monolaurate
- Sorbitan Monooleate
Analysis Note
These products are for test and assay use only. They are not meant for administration to humans or animals and cannot be used to diagnose, treat, or cure diseases of any kind.
Other Notes
Sales restrictions may apply.
related product
Product No.
Description
Pricing
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Synthesis and glycosidase inhibitory activity of 1-amino-3,6-anhydro-1-deoxy-D-sorbitol derivatives.
Stéphane Guillarme et al.
Bioorganic chemistry, 38(2), 43-47 (2010-01-12)
3,6-Anhydro-1-(aryl or alkylamino)-1-deoxy-D-sorbitol derivatives have been prepared in four steps from isosorbide, a by-product from the starch industry. The inhibitory activities of these new compounds have been evaluated towards 13 glycosidases. A first lead-compound was identified, which inhibited beta-N-acetylglucosaminidase from
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