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15054-86-1

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15054-86-1 Usage

Description

Ethylene glycol, also known as ethanediol, is an organic compound with the formula (CH2OH)2. It is a colorless, sweet-tasting, and viscous liquid that is miscible with water in all proportions. Ethylene glycol is primarily used as a raw material for the production of various chemicals and as an antifreeze agent in the automotive industry.

Uses

Used in Chemical Synthesis:
Ethylene glycol is used as a starting material for the synthesis of various chemicals, including oxiran-d4. This application is due to its versatile chemical properties, which allow it to be easily converted into a wide range of products.
Used in Automotive Industry:
Ethylene glycol is used as an antifreeze agent in the automotive industry. It is effective in lowering the freezing point of water and raising its boiling point, making it an ideal coolant for car engines. This application is due to its ability to prevent the engine from overheating and its low toxicity compared to other antifreeze agents.
Used in NMR-based Research and Analyses:
Ethylene glycol-d6, a deuterated version of ethylene glycol, is used as an NMR solvent in nuclear magnetic resonance (NMR) research and analyses. This application is because of its clear, colorless liquid properties and its recorded infrared spectrum, which make it suitable for studying molecular structures and interactions.
Used in Different Industries:
Ethylene glycol has various applications across different industries, including:
1. Used in the Plastics Industry:
Ethylene glycol is used as a raw material for the production of polyethylene terephthalate (PET), a widely used plastic in the packaging industry. This application is due to its ability to form polymers with desirable properties, such as strength and flexibility.
2. Used in the Textile Industry:
Ethylene glycol is used in the textile industry as a solvent for dyes and as a humectant to help maintain the moisture content of fibers. This application is because of its ability to dissolve a wide range of substances and its hygroscopic nature.
3. Used in the Pharmaceutical Industry:
Ethylene glycol is used as a solvent and a carrier for various pharmaceutical products, including oral, topical, and injectable medications. This application is due to its compatibility with a wide range of active ingredients and its ability to enhance the solubility and stability of drugs.
4. Used in the Cosmetics Industry:
Ethylene glycol is used in the cosmetics industry as a solvent, humectant, and preservative in various personal care products, such as lotions, creams, and shampoos. This application is because of its ability to improve the texture and consistency of products, as well as its moisturizing and antimicrobial properties.

Check Digit Verification of cas no

The CAS Registry Mumber 15054-86-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,5 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15054-86:
(7*1)+(6*5)+(5*0)+(4*5)+(3*4)+(2*8)+(1*6)=91
91 % 10 = 1
So 15054-86-1 is a valid CAS Registry Number.
InChI:InChI=1/C2H6O2/c3-1-2-4/h3-4H,1-2H2

15054-86-1 Well-known Company Product Price

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  • Alfa Aesar

  • (42288)  Ethylene glycol-d6, 98% (Isotopic)   

  • 15054-86-1

  • 1g

  • 1251.0CNY

  • Detail
  • Alfa Aesar

  • (42288)  Ethylene glycol-d6, 98% (Isotopic)   

  • 15054-86-1

  • 5g

  • 5900.0CNY

  • Detail

15054-86-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethylene Glycol-d (Isotopic)

1.2 Other means of identification

Product number -
Other names Ethylene glycol-d6

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:15054-86-1 SDS

15054-86-1Upstream product

15054-86-1Related news

Highly efficient ETHYLENE GLYCOL (cas 15054-86-1) electrocatalytic oxidation based on bimetallic PtNi on 2D molybdenum disulfide/reduced graphene oxide nanosheets07/23/2019

In this paper, a two-dimensional (2D) hybrid material of molybdenum disulfide (MoS2)/reduced graphene oxide (RGO) is facilely synthesized and used as an ideal support for the deposition of Pt nanoparticles. The as-prepared Pt/MoS2/RGO composites are further worked as electrocatalysts towards eth...detailed

Electro-oxidation of ETHYLENE GLYCOL (cas 15054-86-1) on PtCo metal synergy for direct ETHYLENE GLYCOL (cas 15054-86-1) fuel cells: Reduced graphene oxide imparting a notable surface of action07/22/2019

Slow electro-oxidation reaction and low power output are two major limiting factors in successful commercialization of fuel cell technology. An efficient and stable electro-catalyst with effectual metal combination supported on a durable matrix may provide a viable solution to overcome these iss...detailed

Cellulose conversion to ETHYLENE GLYCOL (cas 15054-86-1) by tungsten oxide-based catalysts07/21/2019

The conversion of cellulose into ethylene glycol remains a significant challenge in the biobased domain. Here we explored the activity of various bulk and mesoporous (doped) tungsten oxides in combination with carbon-supported ruthenium for obtaining ethylene glycol from cellulose. Tungstite and...detailed

15054-86-1Relevant articles and documents

Transfer hydrogenation of organic formates and cyclic carbonates: An alternative route to methanol from carbon dioxide

Kim, Seung Hyo,Hong, Soon Hyeok

, p. 3630 - 3636 (2014)

Transfer hydrogenation of organic formates and cyclic carbonates was achieved for the first time using a readily available ruthenium catalyst. Nontoxic and economical 2-propanol was used, both as a solvent and hydrogen source, without the need of using flammable H2 gas under high pressure. This method provides an indirect strategy to produce methanol from carbon dioxide under mild conditions as well as an operationally simple and environmentally benign way to reduce formates and carbonates.

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