26826-30-2 Usage
Uses
Used in Paints and Coatings Industry:
TRIETHYLENE GLYCOL MONOTETRADECYL ETHER is used as a dispersant for enhancing the stability and performance of paints and coatings. It aids in the even distribution of pigments and other components, improving the final product's quality and durability.
Used in Inks Industry:
In the inks industry, TRIETHYLENE GLYCOL MONOTETRADECYL ETHER serves as a dispersant, ensuring consistent ink flow and color uniformity, which is crucial for high-quality printing.
Used in Cleaning Products:
TRIETHYLENE GLYCOL MONOTETRADECYL ETHER is used as a component in cleaning products, where it helps dissolve and remove various types of dirt and stains, contributing to the effectiveness of the cleaning process.
Used in Adhesives:
As a component in adhesives, TRIETHYLENE GLYCOL MONOTETRADECYL ETHER acts as a solvent that can improve the adhesive's bonding properties and workability.
Used as a Solvent for Nitrocellulose and Cellulose Ethers:
TRIETHYLENE GLYCOL MONOTETRADECYL ETHER is utilized as a solvent for nitrocellulose and cellulose ethers, which are important in the manufacturing of films, coatings, and other cellulose-based products.
Used as a Stabilizer in Metal Working Fluids:
In the metalworking industry, TRIETHYLENE GLYCOL MONOTETRADECYL ETHER is used as a stabilizer in metal working fluids to maintain the fluid's properties and performance during machining processes.
It is important to handle TRIETHYLENE GLYCOL MONOTETRADECYL ETHER with care due to its potential health hazards, such as causing irritation to the skin, eyes, and respiratory system, as well as its potential negative impact on aquatic organisms.
Check Digit Verification of cas no
The CAS Registry Mumber 26826-30-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,8,2 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 26826-30:
(7*2)+(6*6)+(5*8)+(4*2)+(3*6)+(2*3)+(1*0)=122
122 % 10 = 2
So 26826-30-2 is a valid CAS Registry Number.
InChI:InChI=1/C20H42O4/c1-2-3-4-5-6-7-8-9-10-11-12-13-15-22-17-19-24-20-18-23-16-14-21/h21H,2-20H2,1H3
26826-30-2Relevant academic research and scientific papers
Drug carrier based on sulfonium lipidosome structure and preparation method and application of drug carrier
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Paragraph 0049; 0064-0066, (2019/08/14)
The invention relates to the technical field of medicine, in particular to a sulfonium compound shown as a general formula (A), and discloses a preparation method of the compound. The compound is poly-condensed with genes to form a nanometer compound with the particle size of 100-300 nm and Zeta potential of +20-+40. The gene loading capability of the sulfonium compound enables the sulfonium compound to have potential application in gene transfer.
Combinatorial synthesis of PEG oligomer libraries
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Page/Page column 9, (2010/02/15)
A simple chain-extending approach was established for the scale-up of the monoprotected monodisperse PEG diol materials. Reactions of THP-(OCH2CH2)n—OMs (n=4, 8, 12) with a large excess of commercially available H—(OCH2CH2)n—OH (n=1-4) under basic conditions led to THP-(OCH2CH2)n—OH (n=5-15). Similarly, Me-(OCH2CH2)n—OH (n=4-11, 13) were prepared from Me-(OCH2CH2)n—OMs (n=3, 7, 11). For the chain elongation steps, 40-80% yields were achieved through extraction purification. PEG oligomer libraries I and II were generated in 50-95% overall yields by alkylation or acylation of THP-(OCH2CH2)n—OH (n=1-15) followed by deprotection. Alkylation of Me-(OCH2CH2)n—OH (n=1-11, 13) with X—(CH2)m—CO2R (X=Br or OMs) and subsequent hydrolysis led to PEG oligomer library III in 30-60% overall yields. Combinatorial purification techniques were adapted to the larger-scale library synthesis. A total of 498 compounds, each with a weight of 2-5 g and a minimum purity of 90%, were synthesized.
