30571-56-3

Usage

Uses

Used in Candy Manufacturing:
SYRUP is used as a sweetening agent for enhancing the taste and texture of candies. Its high sugar content provides the desired sweetness and contributes to the formation of the candy's structure.
Used in Soft Drink Industry:
In the soft drink industry, SYRUP is used as a primary ingredient to add sweetness and flavor to beverages. It is often mixed with carbonated water, flavorings, and other additives to create a wide range of soft drinks.
Used in Soda-Fountain Goods:
SYRUP is used as a key component in the preparation of various soda-fountain goods, such as flavored syrups for fountain drinks, milkshakes, and smoothies. Its viscosity and sweetness play a crucial role in achieving the desired taste and consistency of these products.
Used in Pharmaceutical Industry:
SYRUP is also used in the pharmaceutical industry as a vehicle for delivering medications, particularly in the form of cough syrups and elixirs. Its thick, viscous nature helps to coat the throat and provide relief from cough and irritation.
Used in Cosmetics and Personal Care Industry:
In the cosmetics and personal care industry, SYRUP is used as an ingredient in various products such as lotions, creams, and shampoos. Its humectant properties help to retain moisture and provide a smooth, silky texture to the products.
Used in Food Industry:
SYRUP is widely used in the food industry as a natural sweetener and flavor enhancer. It is commonly found in baked goods, desserts, and confectionery items, where it adds sweetness, moisture, and a rich taste to the final product.

Defination

Commercial name for an aqueous solution of cane or beet sugar (sucrose) sold in tank car lots to manufacturers of candy, soft drinks, soda-fountain goods, etc. USP grade is an aqueous solution of cane sugar (85 g/100 mL). A viscous liquid with d 1.313.

InChI:InChI=1/C13H18O9/c1-7(15)19-6-12(21-9(3)17)13(22-10(4)18)11(5-14)20-8(2)16/h5,11-13H,6H2,1-4H3

Upstream product

• 7226-49-5 2,3,4,5-tetra-O-acetyl-D-xylose diethyl dithioacetal 
• 59-23-4 D-Galactose 
• 108-24-7 acetic anhydride 
• 58-86-6 D-xylose 

Downstream Products

• 7208-41-5 penta-O-acetyl-6-deoxy-L-glucitol 
• 7208-41-5 penta-O-acetyl-1-deoxy-D-iditol 
• 3615-56-3 D-Sorbose 
• 86334-50-1 1-deoxy-D-gulitol 

Relevant academic research and scientific papers

Indiosides G-K: Steroidal glycosides with cytotoxic and anti-inflammatory activities from Solanum violaceum

Five new steroidal glycosides (1-5) and nine known compounds were isolated from Solanum violaceum. Indiosides G (1) and H (2) are spirostene saponins with an iso-type F ring, indioside I (3) is a spirostane saponin, and indiosides J (4) and K (5) are unusual furostanol saponins with a deformed F ring. These structures represent rare naturally occurring steroidal skeletons. The structures of the new compounds were elucidated using 1D and 2D spectroscopic techniques and acid hydrolysis. Compounds 2, 3, and 7-9 exhibited cytotoxic activity against six human cancer cell lines (HepG2, Hep3B, A549, Ca9-22, MDA-MB-231, and MCF-7) with IC50 values of 1.83-8.04 μg/mL. Steroidal saponins 3, 8, and 9 showed inhibitory effects on superoxide anion generation with IC50 values of 2.84 ± 0.18, 0.62 ± 0.03, and 1.62 ± 0.59 μg/mL, respectively. Saponins 8 and 9 also inhibited elastase release with IC50 values of 111.05 ± 7.37 and 4.04 ± 0.51 μg/mL, respectively. Structure-activity relationship correlations of these compounds with respect to cytotoxic and anti-inflammatory effects are discussed.

Tandem epoxidation-alcoholysis or epoxidation-hydrolysis of glycals catalyzed by titanium(IV) isopropoxide or Venturello's phosphotungstate complex

Venturello's phosphotungstate complex and titanium(IV) isopropoxide [Ti(O-i-Pr)4] were successfully used as catalysts for the epoxidation-alcoholysis of glycals using hydrogen peroxide [H2O 2]. Reaction substrates included a range of variously protected glycals and different alcohols were used as solvents. Ti(O-i-Pr)4 was only effective in methanol as solvent, but gave methyl glycosides in high yields and high selectivities. The Venturello complex proved to be a very versatile and efficient catalyst. Apart from epoxidation-alcoholysis in alcoholic solvents it also showed activity in biphasic conditions to allow for glycosylation of long-chain alcohols and was very effective in the stereoselective dihydroxylation of benzylated glucal.

C-GLYCOSIDE ANALOGUES OF N-(4-HYDROXYPHENYL)RETINAMIDE-O-GLUCURONIDE

The present invention provides breast cancer chemopreventive arylamide analogues of retinoic acid, more particularly C-glycoside analogues of N-(4-hydroxyphenyl)retinamide-O-glucuronide and N-glycoside analogue of retinoyl beta-glucuronide that resist both beta-glucuronidase mediated enzymatic hydrolysis as well as acid catalyzed hydrolysis. Specifically, the drugs include 4-(retinamido)phenyl-C-glucuronide; 4-(retinamido)phenyl-C-glucoside; 4-(retinamido)benzyl-C-xyloside; 4-(retinamido)benzyl-C-glucoside; 4-(retinamido)benzyl-C-glucuronide; 4-(retinamido)phenyl-C-xyloside, 1-(B-D-lucopyranosyl) retinamide and 1-(D-glucopyranosyluronosly) retinamide. The invention also relates to a method for making such drugs.

PYRIDINDOLOL ANALOGUES. SYHTHESIS OF 3-HYDROXYMETHYL-1-(POLYHYDROXYALKYL)-β-CARBOLINES

Peracetylated (D)-glucose, (D)-galactose, (D)-ribose, (L)-arabinose and (D)-xylose have been subjected to a Pictet-Spengler cyclisation with methyl tryptophanate to give β-carboline derivatives which have been converted to a series of pyridindolol analogues.