Difference between revisions of "Inositol"
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| OtherNames = cis-1,2,3,5-trans-4,6-Cyclohexanehexol<br>Cyclohexanehexol<br>Mouse antialopecia factor<br>Nucite<br>Phaseomannite<br>Phaseomannitol | | OtherNames = cis-1,2,3,5-trans-4,6-Cyclohexanehexol<br>Cyclohexanehexol<br>Mouse antialopecia factor<br>Nucite<br>Phaseomannite<br>Phaseomannitol | ||
<!-- Images --> | <!-- Images --> | ||
− | | ImageFile = | + | | ImageFile = Myo_Inositol.jpg |
− | | ImageSize = | + | | ImageSize = 270px |
| ImageAlt = | | ImageAlt = | ||
| ImageName = | | ImageName = | ||
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| BoilingPtC = | | BoilingPtC = | ||
| BoilingPt_ref = | | BoilingPt_ref = | ||
− | | BoilingPt_notes = | + | | BoilingPt_notes = Decomposes |
| Density = 1.752 g/cm<sup>3</sup> | | Density = 1.752 g/cm<sup>3</sup> | ||
| Formula = C<sub>6</sub>H<sub>12</sub>O<sub>6</sub> | | Formula = C<sub>6</sub>H<sub>12</sub>O<sub>6</sub> | ||
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| MeltingPt_ref = | | MeltingPt_ref = | ||
| MeltingPt_notes = | | MeltingPt_notes = | ||
+ | | Odor = Odorless | ||
| pKa = | | pKa = | ||
| pKb = | | pKb = | ||
− | | Solubility = 14 g/100 ml (25 ºC) | + | | Solubility = 14 g/100 ml (25 ºC), <br/> 28 g/100 mL (60 °C)<ref>W.L.F. Armarego, C.L.L. Chai, Purification of Laboratory Chemicals (Sixth Edition), |
− | | SolubleOther = Moderate soluble in [[methanol]]<br>Slightly soluble in [[Dimethyl sulfoxide|DMSO]]<br>Insoluble in alcohols, [[dichloromethane]], [[dimethylformamide]], [[tetrahydrofuran]]<ref>https://www.researchgate.net/post/Does_anyone_know_about_solubility_of_Inositol_except_for_water</ref> | + | Butterworth-Heinemann, 2009, ISBN 9781856175678, p. 693</ref> |
+ | | SolubleOther = Moderate soluble in [[methanol]]<br>Slightly soluble in [[Dimethyl sulfoxide|DMSO]], [[ethanol]]<br>Insoluble in alcohols, [[dichloromethane]], [[dimethylformamide]], [[tetrahydrofuran]]<ref>https://www.researchgate.net/post/Does_anyone_know_about_solubility_of_Inositol_except_for_water</ref>, [[diethyl ether]]<ref>W.L.F. Armarego, C.L.L. Chai, Purification of Laboratory Chemicals (Sixth Edition), | ||
+ | Butterworth-Heinemann, 2009, ISBN 9781856175678, p. 693</ref> | ||
| Solvent = | | Solvent = | ||
− | | VaporPressure = | + | | VaporPressure = ~0 mmHg |
}} | }} | ||
| Section3 = {{Chembox Structure | | Section3 = {{Chembox Structure | ||
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==Properties== | ==Properties== | ||
===Chemical=== | ===Chemical=== | ||
− | Inositol can be nitrated to give inositol hexanitrate. | + | Inositol can be nitrated to give inositol hexanitrate using a [[nitrating mixture]]. |
Oxidation with nitric acid gives rhodizonic acid. | Oxidation with nitric acid gives rhodizonic acid. | ||
+ | |||
+ | Inositol may be recrystallized from water or 50% ethanol/water, from which a dihydrate results. It may be dehydrated to a non-hygroscopic anhydrous form.<ref>W.L.F. Armarego, C.L.L. Chai, Purification of Laboratory Chemicals (Sixth Edition), | ||
+ | Butterworth-Heinemann, 2009, ISBN 9781856175678, p. 692</ref> | ||
===Physical=== | ===Physical=== | ||
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==Availability== | ==Availability== | ||
− | Inositol is available in many health food stores. | + | Inositol is available in many health food stores. It is sold as a food supplement, sometimes mixed with taurine. |
It can also be bought online cheaply. | It can also be bought online cheaply. | ||
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===Storage=== | ===Storage=== | ||
− | Inositol should be kept in closed bottles. | + | Inositol should be kept in closed bottles, plastic bottles are sufficient. |
===Disposal=== | ===Disposal=== |
Latest revision as of 21:41, 27 February 2021
Names | |
---|---|
IUPAC name
(1R,2R,3S,4S,5R,6S)-cyclohexane-1,2,3,4,5,6-hexol
| |
Other names
cis-1,2,3,5-trans-4,6-Cyclohexanehexol
Cyclohexanehexol Mouse antialopecia factor Nucite Phaseomannite Phaseomannitol | |
Properties | |
C6H12O6 | |
Molar mass | 180.16 g/mol |
Appearance | White solid |
Odor | Odorless |
Density | 1.752 g/cm3 |
Melting point | 225–227 °C (437–441 °F; 498–500 K) |
Boiling point | Decomposes |
14 g/100 ml (25 ºC), 28 g/100 mL (60 °C)[1] | |
Solubility | Moderate soluble in methanol Slightly soluble in DMSO, ethanol Insoluble in alcohols, dichloromethane, dimethylformamide, tetrahydrofuran[2], diethyl ether[3] |
Vapor pressure | ~0 mmHg |
Hazards | |
Safety data sheet | Sigma-Aldrich (myo-inositol) |
Flash point | 143 °C |
Lethal dose or concentration (LD, LC): | |
LD50 (Median dose)
|
10,000 mg/kg (mouse, oral) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Inositol or cyclohexane-1,2,3,4,5,6-hexol is a chemical compound with formula C6H12O6, a sugar alcohol. It exists in nine possible stereoisomers, of which the most prominent form, widely occurring in nature, is cis-1,2,3,5-trans-4,6-cyclohexanehexol, or myo-inositol (former names meso-inositol or i-inositol). Its taste has been assayed at half the sweetness of table sugar (sucrose).
Contents
Properties
Chemical
Inositol can be nitrated to give inositol hexanitrate using a nitrating mixture.
Oxidation with nitric acid gives rhodizonic acid.
Inositol may be recrystallized from water or 50% ethanol/water, from which a dihydrate results. It may be dehydrated to a non-hygroscopic anhydrous form.[4]
Physical
Inositol is a crystalline solid, soluble in water.
Availability
Inositol is available in many health food stores. It is sold as a food supplement, sometimes mixed with taurine.
It can also be bought online cheaply.
Preparation
Inositol is best bought than made.
Projects
- Make rhodizonic acid and potassium rhodizonate
- Make inositol hexanitrate
Handling
Safety
Inositol has low toxicity and it's 100% edible. Lab-grade inositol however, isn't.
Storage
Inositol should be kept in closed bottles, plastic bottles are sufficient.
Disposal
Inositol doesn't require special disposal. Discard it as you wish.
References
- ↑ W.L.F. Armarego, C.L.L. Chai, Purification of Laboratory Chemicals (Sixth Edition), Butterworth-Heinemann, 2009, ISBN 9781856175678, p. 693
- ↑ https://www.researchgate.net/post/Does_anyone_know_about_solubility_of_Inositol_except_for_water
- ↑ W.L.F. Armarego, C.L.L. Chai, Purification of Laboratory Chemicals (Sixth Edition), Butterworth-Heinemann, 2009, ISBN 9781856175678, p. 693
- ↑ W.L.F. Armarego, C.L.L. Chai, Purification of Laboratory Chemicals (Sixth Edition), Butterworth-Heinemann, 2009, ISBN 9781856175678, p. 692