80999
1L-epi-2-Inosose
≥98.0% (HPLC)
Synonym(s):
(2R,3S,4S,5S,6S)-2,3,4,5,6-Pentahydroxycyclohexanone, 2L-2,3,4,6/5-Pentahydroxycyclohexanone, D-epi-4-Inosose, L-epi-2-Inosose
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Empirical Formula (Hill Notation):
C6H10O6
CAS Number:
Molecular Weight:
178.14
UNSPSC Code:
12352201
NACRES:
NA.25
MDL number:
Beilstein/REAXYS Number:
3199555
Quality Level
InChI
1S/C6H10O6/c7-1-2(8)4(10)6(12)5(11)3(1)9/h1-5,7-11H/t1-,2-,3-,4+,5-/m0/s1
InChI key
VYEGBDHSGHXOGT-PKTMPMCPSA-N
assay
≥98.0% (HPLC)
form
crystals
optical activity
[α]/D -4.3±1.3°, c = 1 in H2O
storage temp.
2-8°C
Biochem/physiol Actions
Metabolite of inositol metabolic pathways
Other Notes
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
Storage Class
11 - Combustible Solids
wgk
WGK 3
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Kinetics and mechanism of the chromic oxidation of myo-inositol
Santoro, M., et al.
Polyhedron, 26, 169-177 (2007)
(-)-epi-Inosose-2
Acta Crystallographica Section C, Structural Chemistry, C56(12), e584-e585 (2000)
Bacterial enzyme preparations oxidizing inositol and their inhibition by colchicine.
R E FRANZL et al.
Nature, 168(4283), 955-957 (1951-12-01)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service