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SAENTA, also known as Glycerol, is a simple polyol compound that is widely used in various industries due to its unique properties. It is a colorless, odorless, and viscous liquid with a sweet taste. Glycerol is hygroscopic, meaning it can absorb water from the environment, and it is also a versatile solvent for various substances. Its hydroxyl groups allow it to form hydrogen bonds with other molecules, making it a valuable component in many applications.

130117-76-9

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130117-76-9 Usage

Uses

Used in Pharmaceutical Industry:
SAENTA is used as a solvent for various pharmaceutical formulations, such as elixirs, syrups, and liquid medications. Its ability to dissolve a wide range of substances, including drugs, makes it an ideal choice for this application.
Used in Cosmetics and Personal Care Industry:
SAENTA is used as a humectant in cosmetics and personal care products, such as lotions, creams, and toothpaste. Its hygroscopic nature helps to retain moisture, providing hydration and improving the texture of these products.
Used in Food and Beverage Industry:
SAENTA is used as a humectant, sweetener, and preservative in the food and beverage industry. It helps to maintain the moisture content in foods, enhances the sweetness of products, and extends their shelf life.
Used in Industrial Applications:
SAENTA is used as a component in the production of various industrial products, such as antifreeze, lubricants, and explosives. Its versatility and compatibility with other substances make it a valuable ingredient in these applications.
Used in Energy Storage:
SAENTA is used as a component in the production of lithium-ion batteries, specifically as an additive to improve the performance and safety of these energy storage devices.
Used as a Novel Ligand:
SAENTA is used as a novel ligand with high affinity for polypeptides associated with nucleoside transport. This application is particularly relevant in the field of molecular biology and drug development, where understanding and manipulating nucleoside transport is crucial for the development of new therapeutic strategies.

Check Digit Verification of cas no

The CAS Registry Mumber 130117-76-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,1,1 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 130117-76:
(8*1)+(7*3)+(6*0)+(5*1)+(4*1)+(3*7)+(2*7)+(1*6)=79
79 % 10 = 9
So 130117-76-9 is a valid CAS Registry Number.
InChI:InChI=1/C19H23N7O5S/c20-5-6-32-8-13-15(27)16(28)19(31-13)25-10-24-14-17(22-9-23-18(14)25)21-7-11-1-3-12(4-2-11)26(29)30/h1-4,9-10,13,15-16,19,27-28H,5-8,20H2,(H,21,22,23)/t13-,15-,16-,19-/m1/s1

130117-76-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name SAENTA

1.2 Other means of identification

Product number -
Other names 5'-S-(2-Aminoethyl)-N6-[(4-nitrobenzyl)-5'-thioadenosine

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:130117-76-9 SDS

130117-76-9Relevant academic research and scientific papers

Improved syntheses of 5′- S -(2-Aminoethyl)-6- N -(4-nitrobenzyl)- 5′-thioadenosine (SAENTA), analogues, and fluorescent probe conjugates: Analysis of cell-surface human equilibrative nucleoside transporter 1 (hENT1) levels for prediction of the antitumor

Robins, Morris J.,Peng, Yunshan,Damaraju, Vijaya L.,Mowles, Delores,Barron, Geraldine,Tackaberry, Tracey,Young, James D.,Cass, Carol E.

experimental part, p. 6040 - 6053 (2010/11/02)

5′-S-(2-Aminoethyl)-6-N-(4-nitrobenzyl)-5′-thioadenosine (SAENTA), 5′-S-(2-acetamidoethyl)-6-N-[(4-substituted)benzyl]-5′- thioadenosine analogues, 5′-S-[2-(6-aminohexanamido)]ethyl-6-N-(4- nitrobenzyl)-5′-thioadenosine (SAHENTA), and related compounds we

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