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Sucrose octasulfate sodium salt, also known as sodium sucrose octasulfate, is a chemical compound derived from sucrose. It is characterized by its white powder form and has been recognized for its cytoprotective properties, making it a valuable component in various applications across different industries.

74135-10-7

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74135-10-7 Usage

Uses

Used in Pharmaceutical Industry:
Sucrose octasulfate sodium salt is used as a reference standard for the drug Sucralfate, which is utilized in the treatment and management of gastrointestinal ulcers. Its cytoprotective effects contribute to the prevention and healing of ulcers in the gastrointestinal tract.
Used in Cosmetics Industry:
In the cosmetics industry, sucrose octasulfate sodium salt is used as an ingredient in various skin care products. The sodium compounds derived from this chemical compound offer protective and beneficial properties for the skin, enhancing the overall effectiveness of these cosmetic formulations.
Used in Oncology:
Sucrose octasulfate sodium salt has been evaluated in patients with cancer for the prevention and management of radiodermatitis, a skin condition that can result from radiation therapy. Its cytoprotective properties help in mitigating the adverse effects of radiation on the skin, providing relief and support to cancer patients undergoing treatment.

Check Digit Verification of cas no

The CAS Registry Mumber 74135-10-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,1,3 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 74135-10:
(7*7)+(6*4)+(5*1)+(4*3)+(3*5)+(2*1)+(1*0)=107
107 % 10 = 7
So 74135-10-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H22O35S8.8Na/c13-48(14,15)37-1-4-6(43-51(22,23)24)8(45-53(28,29)30)9(46-54(31,32)33)11(40-4)42-12(3-39-50(19,20)21)10(47-55(34,35)36)7(44-52(25,26)27)5(41-12)2-38-49(16,17)18;;;;;;;;/h4-11H,1-3H2,(H,13,14,15)(H,16,17,18)(H,19,20,21)(H,22,23,24)(H,25,26,27)(H,28,29,30)(H,31,32,33)(H,34,35,36);;;;;;;;/q;8*+1/p-8/t4-,5-,6-,7-,8+,9-,10+,11-,12+;;;;;;;;/m1......../s1

74135-10-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Sucrose octasulfate sodium salt

1.2 Other means of identification

Product number -
Other names sucrose octasulphate sodium salt

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:74135-10-7 SDS

74135-10-7Downstream Products

74135-10-7Relevant academic research and scientific papers

HYPERSULFATED GLUCOPYRANOSIDES

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Page/Page column 10; 11, (2011/10/13)

Hypersulfated disaccharides, preferably octasulfated sucrose, with utility in asthma or asthma related disorders are disclosed. The compounds may optionally be formulated with pharmaceutically acceptable excipients or delivery agents. The delivery agents are selected from the group consisting of natural or synthetic polymers, aerosols or other vehicles that facilitate the delivery or administration of the drug. The hypersulfated disaccharides are made from carbohydrate starting materials. Ion exchange or other suitable synthetic processes may be utilized to prepare the pharmaceuticals. The hypersulfated disaccharides are useful as anti-inflammatory agents.

Tissue distribution of [14C]sucrose octasulfate following oral administration to rats.

Hiebert, Linda M,Wice, Sandra M,Ping, Tidly,Hileman, Ronald E,Polat, Tfilay,Linhardt, Robert J

, p. 838 - 844 (2007/10/03)

PURPOSE: Aluminum sucrose octasulfate (SOS) is used clinically to prevent ulcers. Under physiologic conditions, the sodium salt of this drug can be formed. Our objective was to determine whether sodium SOS was absorbed when administered orally. In addition to furthering our understanding of aluminum SOS, this study also aimed to clarify how other polyanionic drugs, such as heparin and low-molecular-weight heparins, are absorbed. METHODS: [14C]-labeled and cold sodium SOS (60 mg/kg) were given to rats by stomach tube. Radioactivity was counted in gut tissue, gut washes, and nongut tissue (i.e., lung, liver, kidney, spleen, endothelial, and plasma samples) at 3 min, 6 min, 15 min, 30 min, 60 min, 4 h, and 24 h, and in urine and feces accumulated over 4 h and 24 h. RESULTS: Peak radioactivity was found in the tissue and washes of the stomach, ileum, and colon at 6 min, 60 min, and 4 h, respectively, showing progression through the gut. Gut recovery accounted for 84% of the dose at 6 min but only 12% of the dose at 24 h, including counts from feces. Radioactivity was recovered from nongut tissue (averaging 8.6% of the dose) and accumulated urine (18% of the dose at 24 h). When total body distribution was considered, the recovery of radioactivity was greater for the endothelium than for plasma (peak percentage of the dose was 65% at 15 min, 20% at 3 min, 5% from 20 to 240 min for the vena cava, aortic endothelium, and plasma, respectively). CONCLUSIONS: Results indicate that sodium SOS is absorbed, agreeing with previous studies demonstrating the oral absorption of other sulfated polyanions. Endothelial concentrations must be considered when assessing the pharmacokinetics of these compounds. The measured plasma drug concentrations reflect the much greater amounts of drug residing with the endothelium.

Method for preparing high potency sucralfate

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, (2008/06/13)

Sucralfate is prepared in good yields and in newly useful form first by reacting sucrose with chlorosulfonic acid in 2-picoline. The amonium salt is then formed and reacted with aluminum chlorohydrate in specific sequence and alcoholic solvent. The two distinct products have unexpected pharmaceutical and physical characteristics. The oral liquid suspensions also must be critically formulated.

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