527-31-1 Usage
Description
HEXAKETOCYCLOHEXANE OCTAHYDRATE 97, also known as Glycerol, is a colorless, odorless, and viscous liquid that is a humectant, solvent, and sweet-tasting substance. It is a simple polyol compound and a sugar alcohol with three hydroxyl groups. Glycerol is widely used in various industries due to its unique properties and versatility.
Uses
Used in Pharmaceutical Industry:
HEXAKETOCYCLOHEXANE OCTAHYDRATE 97 is used as a humectant and solvent for the production of various pharmaceutical formulations, such as elixirs, syrups, and suppositories. Its humectant properties help maintain the moisture content in these formulations, while its solvent properties enable the dissolution of various active ingredients.
Used in Cosmetics and Personal Care Industry:
HEXAKETOCYCLOHEXANE OCTAHYDRATE 97 is used as a moisturizer and humectant in cosmetics and personal care products, such as lotions, creams, and shampoos. Its ability to attract and retain water helps maintain the hydration and suppleness of the skin, while also providing a smooth and pleasant texture to the products.
Used in Food and Beverage Industry:
HEXAKETOCYCLOHEXANE OCTAHYDRATE 97 is used as a humectant, emulsifier, and sweetener in the food and beverage industry. It helps maintain the moisture content in various food products, such as baked goods, confectionery, and jams, while also improving their texture and shelf life. Additionally, it is used as a sweetener in low-calorie and sugar-free products due to its sweet taste.
Used in Chemical and Industrial Applications:
HEXAKETOCYCLOHEXANE OCTAHYDRATE 97 is used as a raw material in the preparation of various chemicals, such as hexaazatriphenylenehexacarbonitrile. Its unique chemical properties, including its beige to grey-brown powder form, make it suitable for use in the synthesis of complex organic compounds and other chemical reactions.
Used in Biodiesel Production:
HEXAKETOCYCLOHEXANE OCTAHYDRATE 97 is used as a component in the production of biodiesel, an alternative and renewable source of energy. Its properties enable it to act as an emulsifier, improving the blending of biodiesel with conventional diesel fuels and enhancing the overall fuel performance.
Check Digit Verification of cas no
The CAS Registry Mumber 527-31-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,2 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 527-31:
(5*5)+(4*2)+(3*7)+(2*3)+(1*1)=61
61 % 10 = 1
So 527-31-1 is a valid CAS Registry Number.
InChI:InChI=1/C6O6.8H2O/c7-1-2(8)4(10)6(12)5(11)3(1)9;;;;;;;;/h;8*1H2
527-31-1Relevant articles and documents
Ultrafast photoinduced electron transfer in face-to-face charge-transfer π-complexes of planar porphyrins and hexaazatriphenylene derivatives
Aoki, Toru,Sakai, Hayato,Ohkubo, Kei,Sakanoue, Tomo,Takenobu, Taishi,Fukuzumi, Shunichi,Hasobe, Taku
, p. 1498 - 1509 (2015/02/05)
Charge-transfer (CT) π-complexes are formed between planar porphyrins and 1,4,5,8,9,12-hexaazatriphenylene (HAT) derivatives with large formation constants (e.g., 104 M-1), exhibiting broad CT absorption bands. The unusually large formation constants result from close face-to-face contact between two planar π-planes of porphyrins and HAT derivatives. The redox potentials of porphyrins and HAT derivatives measured by cyclic voltammetry indicate that porphyrins and HAT derivatives act as electron donors and acceptors, respectively. The formation of 1:1 CT complexes between porphyrins and HAT derivatives was examined by UV-vis, fluorescence and 1H NMR measurements in nonpolar solvents. The occurrence of unprecedented ultrafast photoinduced electron transfer from the porphyrin unit to the HAT unit in the CT π-complex was observed by femtosecond laser flash photolysis measurements. A highly linear aggregate composed of a planar porphyrin and an HAT derivative was observed by transmission electron microscopy (TEM) and atomic force microscopy (AFM).
The photochemistry of the rhodizonate dianion in aqueous solution
Iraci, G.,Back, M. H.
, p. 1293 - 1294 (2007/10/02)
The photochemistry of the rhodizonate dianion at 483 nm has been studied in aqueous solution at pH 8.3.In the absence of oxygen no reaction was observed.In the presence of oxygen, 6.2 x 10-5 M, the dianion was consumed with a quantum yield of 0.044.The oxidation apparently did not involve the formation of O2(1Δg).Electron transfer from the excited dianion was observed with methyl viologen.