17643-17-3 Usage
Description
2-Mercaptoethoxy ethanol, also known as 2-(2-Mercaptoethoxy)ethanol, is an organic compound with the chemical formula C4H10O2S. It is a colorless to slightly yellow liquid with a characteristic odor. The molecule contains a thiol (-SH) group, an ether group, and two hydroxyl groups, which contribute to its unique chemical properties and reactivity.
Uses
Used in Chemical Synthesis:
2-Mercaptoethoxy ethanol is used as a reagent in the synthesis of various organic compounds, particularly in the pharmaceutical and chemical industries. Its thiol and hydroxyl groups make it a versatile building block for the creation of new molecules with potential applications in drug development and material science.
Used in Curing Type Hydrotreating Catalysts:
In the petrochemical industry, 2-Mercaptoethoxy ethanol is utilized in the preparation method of curing type hydrotreating catalysts. Hydrotreating is a crucial process for removing sulfur and nitrogen impurities from petroleum products, and 2-Mercaptoethoxy ethanol plays a role in enhancing the catalyst's performance and efficiency in this process.
Used in Antioxidant Formulations:
Due to its thiol group, 2-Mercaptoethoxy ethanol can act as an antioxidant, which is beneficial in the stabilization of various industrial products, such as plastics, rubber, and lubricants. It helps prevent oxidative degradation, extending the shelf life and improving the performance of these materials.
Used in Personal Care Products:
In the cosmetics and personal care industry, 2-Mercaptoethoxy ethanol is employed as a reducing agent and stabilizer. It is commonly used in hair care products, such as perms and hair color treatments, to help break and reform disulfide bonds in hair proteins, allowing for easier styling and coloring.
Used in Analytical Chemistry:
2-Mercaptoethoxy ethanol is also used in analytical chemistry as a protecting agent for thiol groups during peptide synthesis and as a scavenger for heavy metal ions in various analytical techniques. Its ability to form stable complexes with metal ions makes it a valuable tool in research and quality control processes.
Check Digit Verification of cas no
The CAS Registry Mumber 17643-17-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,4 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17643-17:
(7*1)+(6*7)+(5*6)+(4*4)+(3*3)+(2*1)+(1*7)=113
113 % 10 = 3
So 17643-17-3 is a valid CAS Registry Number.
17643-17-3Relevant articles and documents
Critical role of surface hydration on the dynamics of serum adsorption studied with monoethylene glycol adlayers on gold
Avci, Ceren,Sheikh, Sonia,Blaszykowski, Christophe,Thompson, Michael
, p. 466 - 468 (2013)
The dynamics of serum adsorption on bare and monoethylene glycol adlayer-modified gold surfaces is investigated using acoustic wave physics. Hydration experiments support the pivotal role ascribed to water in the antifouling of surfaces. Behavioural discr
SELF DELIVERING BIO-LABILE PHOSPHATE PROTECTED PRO-OLIGOS FOR OLIGONUCLEOTIDE BASED THERAPEUTICS AND MEDIATING RNA INTERFERENCE
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Page/Page column title page; 105-106, (2010/04/27)
Disclosed herein are compositions and methods for generating ribo-nucleic neutral (RNN) or deoxyribo-nucleic-neutral (DNN) polynucleotides with reduced anionic charge, for improved intracellular delivery. Also disclosed herein are methods of using RNN and DNN compositions.
