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20461-54-5

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20461-54-5 Usage

Description

Iodide oil, also known as an iodine addition product, is a thick, viscous, oily liquid derived from vegetable oil or oils containing 38-42% organically combined iodine. It is affected by air and light and is soluble in solvent naphtha.

Uses

Used in Pharmaceutical Industry:
Iodide oil is used as a pharmaceutical agent for its antiseptic and disinfectant properties. It is particularly effective in treating various skin conditions and infections due to its ability to kill bacteria and other microorganisms.
Used in Radiology:
In the field of radiology, iodide oil is used as a contrast agent for imaging procedures such as X-rays and CT scans. Its high iodine content allows for better visualization of blood vessels and other internal structures during the examination.
Used in Cosmetic Industry:
Iodide oil is also used in the cosmetic industry as an ingredient in various skin care products. Its antiseptic and disinfectant properties make it suitable for treating acne, reducing inflammation, and promoting skin healing.
Used in Veterinary Medicine:
In veterinary medicine, iodide oil is used as a treatment for various skin conditions and infections in animals. Its broad-spectrum antimicrobial activity makes it an effective option for treating a wide range of bacterial, fungal, and viral infections.
Used in Industrial Applications:
Iodide oil is used in the industrial sector for its lubricating properties. Its thick, viscous nature makes it an ideal choice for use in machinery and equipment that require a high-quality lubricant to reduce friction and prevent wear.
Used in Research and Development:
In the field of research and development, iodide oil is used as a starting material for the synthesis of various iodine-containing compounds. Its unique chemical properties make it a valuable resource for the development of new pharmaceuticals, chemicals, and materials.

Hazard

Toxic by ingestion.

Check Digit Verification of cas no

The CAS Registry Mumber 20461-54-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,4,6 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 20461-54:
(7*2)+(6*0)+(5*4)+(4*6)+(3*1)+(2*5)+(1*4)=75
75 % 10 = 5
So 20461-54-5 is a valid CAS Registry Number.
InChI:InChI=1/HI/h1H/p-1

20461-54-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name iodide

1.2 Other means of identification

Product number -
Other names iodinane

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:20461-54-5 SDS

20461-54-5Relevant articles and documents

Influence of external electric fields on reaction fronts in the iodate-arsenous acid system

Forstova, Lenka,Sevcikova, Hana,Marek, Milos,Merkin, John H.

, p. 9136 - 9143 (2000)

The propagation of arsenous acid-iodate reaction fronts of different net stoichiometries in externally applied dc electric fields is studied for a range of both electric field intensities and initial compositions of the reacting mixture (represented by the stoichiometric factor S0). Regions of three different types of net stoichiometry in the parametric space E/V vs S0, where E is the intensity of the applied electric field and V the reaction front propagation velocity, are determined both experimentally and by analyzing a reaction-diffusion-migration model that includes a realistic kinetic scheme of the reaction studied. Both agreement with and discrepancies between the theoretical predictions and experimental findings are discussed.

Multinuclear Transition Metal Sandwich-Type Polytungstate Derivatives for Enhanced Electrochemical Energy Storage and Bifunctional Electrocatalysis Performances

Cui, Liping,Dai, Wenting,Lv, Jinghua,Ma, Xinyue,Yu, Kai,Yuan, Jie,Zhou, Baibin

supporting information, (2020/04/02)

Different transition metal (TM) units are introduced into a trivacant Keggin cluster to form three sandwich polytungstate derivatives, (H2en)[{K(H2O)0.5}2{K2(H2O)3}{Ni(H2O)(en)2}2{Ni4(H2O)2(PW9O34)2}] (1), [Cu6(Himi)6{AsIIIW9O33}2]·5H2O (2), and (H2btp)4[FeIII2FeII2(H2O)2(AsW9 O34)2]·4H2O (3) (en = ethanediamine; imi = imidazole; btp = 1,3-bis(1, 2, 4-triazol-1-yl) propane). Compound 1 is a 2,3,8-connected 3D network with {43}2{46·66·83·612·8}{6}2 topology based on bisupported tetra-Ni sandwich phosphotungstate and two kinds of potassium connection units. Compound 2 is a dense 12-connected 3D supramolecular network with {324·436·56} topology based on hexa-Cu(imi) sandwiched arsenotungstate. Compound 3 represents the first mixed valence tetra-Fe substituted sandwich arsenotungstate assembly. Compounds 1-3 show enhanced supercapacitor performance (618.2, 603.4, and 504.6 F·g-1 at a current density of 2.4 A·g-1 with 91.5%, 89.3%, and 87.8% of cycle efficiency after 5000 cycles, respectively) compared to their maternal polyoxometalates (POMs) and most reported POM-based electrode materials, which suggests that the introduction of multinuclear TM into vacant POMs is an effective method to improve the energy storage performance of POMs. In addition, compounds 1 and 3 exhibit dual-functional electrocatalytic behaviors in the reduction of iodate and the oxidation of dopamine for introduction of {Ni4} and {Fe4} units.

Colloidal synthesis of wurtz-stannite Cu2CdGeS4 nanocrystals with high catalytic activity toward iodine redox couples in dye-sensitized solar cells

Huang, Shoushuang,Zai, Jiantao,Ma, Dui,He, Qingquan,Liu, Yuanyuan,Qiao, Qiquan,Qian, Xuefeng

, p. 10866 - 10869 (2016/09/09)

Wurtz-stannite Cu2CdGeS4 nanocrystals were synthesized via a facile hot-injection method at a low temperature. They exhibited low charge transfer resistance at the electrolyte-electrode interface and high electrocatalytic activity for the reduction of I3- in dye-sensitized solar cells (DSSCs). Moreover, this DSSC showed a power conversion efficiency of 7.67%, comparable to the Pt-based device (7.54%).

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