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4433-56-1

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4433-56-1 Usage

Physical state

Liquid

Color

Colorless

Odor

Odorless

Taste

Sweet

Molecular structure

Two hydroxyl (-OH) groups attached to a single carbon-carbon bond

Boiling point

197.3°C (387.1°F)

Melting point

-13.2°C (8.2°F)

Solubility

Highly soluble in water and many organic solvents

Uses

Automotive antifreeze
Production of polyester fibers
Production of resins
Heat transfer fluids
De-icing agent

Toxicity

Highly toxic if ingested
Causes damage to kidneys and central nervous system

Environmental impact

Harmful to the environment
Can contaminate water sources and soil

Handling and disposal

Proper handling and disposal are crucial to prevent harm to humans and the environment

Safety measures

Use personal protective equipment (PPE) and follow safety guidelines when handling 1,1-ethanediol

Check Digit Verification of cas no

The CAS Registry Mumber 4433-56-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,3 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4433-56:
(6*4)+(5*4)+(4*3)+(3*3)+(2*5)+(1*6)=81
81 % 10 = 1
So 4433-56-1 is a valid CAS Registry Number.
InChI:InChI=1/C2H6O2/c1-2(3)4/h2-4H,1H3

4433-56-1SDS

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 ethane-1,1-diol

1.2 Other means of identification

Product number -
Other names 1,1-Dihydroxyethane

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:4433-56-1 SDS

4433-56-1Relevant articles and documents

AEROBIC ELECTROCATALYTIC OXIDATION OF HYDROCARBONS

-

Paragraph 0074, (2022/01/04)

This invention is directed to a method of oxygenating hydrocarbons with molecular oxygen, O2, as oxidant under electrochemical reducing conditions, using polyoxometalate compounds containing copper such as Q10 [Gu4(H2O)2(B-α-PW9O)2] or Q12{ [Cu(H2O)]3[(A-α- PW9O34)2(NO3)-] } or solvates thereof as catalysts, wherein Q are each independently selected from alkali metal cations, alkaline earth metal cations, transition metal cations, NH4+,H+ or any combination thereof.

Electro-catalytic conversion of ethanol in solid electrolyte cells for distributed hydrogen generation

Ju, HyungKuk,Giddey, Sarbjit,Badwal, Sukhvinder P.S.,Mulder, Roger J.

, p. 744 - 757 (2016/07/22)

The global interest in hydrogen/fuel cell systems for distributed power generation and transport applications is rapidly increasing. Many automotive companies are now bringing their pre-commercial fuel cell vehicles in the market, which will need extensive hydrogen generation, distribution and storage infrastructure for fueling of these vehicles. Electrolytic water splitting coupled to renewable sources offers clean on-site hydrogen generation option. However, the process is energy intensive requiring electric energy >4.2?kWh for the electrolysis stack and?>6?kWh for the complete system per m3 of hydrogen produced. This paper investigates using ethanol as a renewable fuel to assist with water electrolysis process to substantially reduce the energy input. A zero-gap cell consisting of polymer electrolyte membrane electrolytic cells with Pt/C and PtSn/C as anode catalysts were employed. Current densities up to 200?mA?cm?2 at 70?°C were achieved at less than 0.75?V corresponding to an energy consumption of about 1.62?kWh?m?3 compared with >4.2?kWh?m?3 required for conventional water electrolysis. Thus, this approach for hydrogen generation has the potential to substantially reduce the electric energy input to less than 40% with the remaining energy provided by ethanol. However, due to performance degradation over time, the energy consumption increased and partial oxidation of ethanol led to lower conversion efficiency. A plausible ethanol electro-oxidation mechanism has been proposed based on the Faradaic conversion of ethanol and mass balance of the by-products identified and quantified using 1H nuclear magnetic resonance spectroscopy and gas chromatography.

Room-temperature acetylene hydration by a Hg(II)-laced metal-organic framework

Yee, Ka-Kit,Wong, Yan-Lung,Zha, Meiqin,Adhikari, Ramesh Y.,Tuominen, Mark T.,He, Jun,Xu, Zhengtao

, p. 10941 - 10944 (2015/06/30)

Thiol (-SH) groups within a Zr(iv)-based metal-organic framework (MOF) anchor Hg(ii) atoms; oxidation by H2O2 then leads to acidic sulfonate functions for catalyzing acetylene hydration at room temperature.

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