CAS 488-58-4|epi-Inositol
| Common Name | epi-Inositol | ||
|---|---|---|---|
| CAS Number | 488-58-4 | Molecular Weight | 180.156 |
| Density | 2.0±0.1 g/cm3 | Boiling Point | 291.3±40.0 °C at 760 mmHg |
| Molecular Formula | C6H12O6 | Melting Point | 304°C(dec.)(lit.) |
| MSDS | ChineseUSA | Flash Point | 143.4±21.9 °C |
Names
| Name | epi-Inositol |
|---|---|
| Synonym | More Synonyms |
epi-Inositol BiologicalActivity
| Description | epi-Inositol is an endogenous metabolite present in Cerebrospinal_Fluid that can be used for the research of Ethanol Consumption[1][2]. |
|---|---|
| Related Catalog | Research Areas >>Others |
| In Vitro | Endogenous metabolites is defined as those that are annotated by Kyoto Encyclopedia of Genes and Genomes as substrates or products of the ~1900 metabolic enzymes encoded in our genome. It is clear in the body of literature that there are documented toxic properties for many of these metabolites[1]. |
| References | [1]. Lee N, et al. Endogenous toxic metabolites and implications in cancer therapy. Oncogene. 2020 Aug;39(35):5709-5720. [2]. Viola A, et al. High cerebral scyllo-inositol: a new marker of brain metabolism disturbances induced by chronic alcoholism. MAGMA. 2004 Sep;17(1):47-61. |
Chemical & Physical Properties
| Density | 2.0±0.1 g/cm3 |
|---|---|
| Boiling Point | 291.3±40.0 °C at 760 mmHg |
| Melting Point | 304°C(dec.)(lit.) |
| Molecular Formula | C6H12O6 |
| Molecular Weight | 180.156 |
| Flash Point | 143.4±21.9 °C |
| Exact Mass | 180.063385 |
| PSA | 121.38000 |
| LogP | -2.11 |
| Vapour Pressure | 0.0±1.4 mmHg at 25°C |
| Index of Refraction | 1.784 |
| Storage condition | 2-8°C |
Safety Information
| RIDADR | NONH for all modes of transport |
|---|---|
| HS Code | 2906199090 |
Customs
| HS Code | 2906199090 |
|---|---|
| Summary | 2906199090. cyclanic, cyclenic or cyclotherpenic alcohols. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0% |
Articles8
More Articles| Synthesis of allo- and epi-inositol via the NHC-catalyzed carbocyclization of carbohydrate-derived dialdehydes. J. Org. Chem. 79(11) , 5088-96, (2014) A synthesis of carbocyclic sugars from carbohydrate-derived dialdehydes using organocatalysis has been developed. Sorbitol, mannitol, and galactitol were converted via 1,6-tritylation, perbenzylation ... | |
| Synthesis of phosphatidylinositols having various inositol stereoisomers by engineered phospholipase D. J. Biosci. Bioeng. 109(4) , 337-40, (2010) Phospholipase D-mediated synthesis of phosphatidylinositols having various inositol stereoisomers was studied. Seven inositol stereoisomers were tested, all of which were found to be substrates of the... | |
| Cyclohexanehexol inhibitors of Abeta aggregation prevent and reverse Alzheimer phenotype in a mouse model. Nat. Med. 12(7) , 801-8, (2006) When given orally to a transgenic mouse model of Alzheimer disease, cyclohexanehexol stereoisomers inhibit aggregation of amyloid beta peptide (Abeta) into high-molecular-weight oligomers in the brain... |
Synonyms
| 1,2,3,4,5,6-Cyclohexanehexol, (1α,2α,3α,4α,5α,6β)- |
| (1R,2R,3r,4S,5S,6s)-1,2,3,4,5,6-Cyclohexanehexol |
| (1R,2R,3r,4S,5S,6s)-Cyclohexane-1,2,3,4,5,6-hexol |
| epi-Inositol |
| 1,2,3,4,5/6-Inositol |
