132144-93-5 Usage
Description
D-SORBITOL-1-13C, also known as Isotope labelled D-Glucitol, is a sugar alcohol derived from the reduction of glucose and is naturally found in various fruits such as apples, pears, and peaches. It is characterized by the presence of a stable isotope, carbon-13, at the first carbon position, which makes it useful for various applications in different industries.
Uses
Used in Food Industry:
D-SORBITOL-1-13C is used as a sweetener for its sugar-like taste and low caloric content, making it a suitable alternative to traditional sugars in the food industry.
Used in Pharmaceutical Industry:
D-SORBITOL-1-13C is used as a laxative due to its osmotic properties, which help promote bowel movement and relieve constipation.
Used in Medical Applications:
D-SORBITOL-1-13C is used in various medical applications, such as a diagnostic tool in metabolic studies, where the isotope-labelled compound can be tracked to understand metabolic pathways and processes.
Used in Cosmetic Products:
D-SORBITOL-1-13C is used in cosmetic products for its moisturizing and humectant properties, helping to maintain skin hydration and improve the texture of the products.
Used in Research and Development:
D-SORBITOL-1-13C is used as a research tool in the development of new drugs and therapies, as the isotope label allows for the tracking of the compound's distribution, metabolism, and interaction with biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 132144-93-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,1,4 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 132144-93:
(8*1)+(7*3)+(6*2)+(5*1)+(4*4)+(3*4)+(2*9)+(1*3)=95
95 % 10 = 5
So 132144-93-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H14O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3-12H,1-2H2/i1+1
132144-93-5Relevant articles and documents
(1-13C)alditols: elimination of magnetic equivalence in 1H- and 13C-n.m.r. spectra of symmetric compounds through (13C)-substitution.
Garrett,Serianni
, p. 23 - 35 (2007/10/02)
(1-13C)Glycerol, D-(1-13C)arabinitol, D-(1-13C)ribitol, D-(1-13C)xylitol, D-(1-13C)glucitol, D-(1-13C)mannitol, and D-(1-13C)talitol have been prepared by NaBH4 reduction of the corresponding (1-13C)aldoses. A comparison of the 1H- (300 and 620 MHz) and 13C (75 MHz) n.m.r. spectra of natural and (1-13C)-substituted dissymmetric alditols has permitted the unequivocal assignments of their hydroxymethyl proton and carbon signals and the measurement of several 13C-1H and 13C-13C spin-coupling constants. Similar spectra of (1-13C)-substituted symmetric alditols, however, are more difficult to interpret since they are composed of overlapping 13C-coupled and 13C-noncoupled subspectra. In some cases, 1H difference spectra and 1H-coupled 13C spectra may be used to extract the 13C-1H and 13C-13C spin couplings from the 13C-coupled component. These couplings have been examined in light of conformational models previously proposed, permitting a preliminary evaluation of standard 3JCH and 3JCC values for specific coupling pathways in these compounds.
