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9004-95-9

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9004-95-9 Usage

Description

POE (20) ISOHEXADECYL ETHER, also known as Polyethylene Glycol Monocetyl Ether or Cetomacrogol 1000, is an off-white waxy solid. It is a nonionic surfactant produced by the ethoxylation of cetyl alcohol to give a material with the general formula HO(C2H4O)nC16H33. Several grades of this material are available depending on the level of ethoxylation performed, with repeat units (n) of polyethylene glycol varying between 2 and 20. Commercially, it can be known as Brij 58 (when n=20) or Brij 56 (when n=10).

Uses

Used in Electronics Industry:
POE (20) ISOHEXADECYL ETHER is used as a surfactant for improving the wetting of PEDOT:PSS, which can further be used in the fabrication of thin film transistors.
Used in Nanotechnology:
POE (20) ISOHEXADECYL ETHER is used as a surfactant for the formation of reverse micelles, which aids in the synthesis of high yielding nanostructures.
Used in Fuel Cell Applications:
POE (20) ISOHEXADECYL ETHER is used in the preparation of platinum electrodes for fuel cell applications.
Used in Cosmetics Industry:
POE (20) ISOHEXADECYL ETHER, also known as ceteth, is used as a surface active agent in cosmetics. It is a compound of derivatives of cetyl, lauryl, stearyl, and oleyl alcohols mixed with ethylene oxide.
Used in Research:
POE (20) ISOHEXADECYL ETHER, or Brij 58, has been used in studies to assess properties of gemini-conventional surfactant mixtures and their effects on solubilization of polycyclic aromatic hydrocarbons. It has also been used in a study to investigate RNase-sensitive constraint of bacterial nucleoid structure.
Used in Food, Cosmetics, and Pharmaceutical Industries:
POE (20) ISOHEXADECYL ETHER is used as a surface active agent, solubilizer, and emulsifying agent in foods, cosmetics, and pharmaceuticals. It is often used as an ointment base and also serves as a research tool.
Used in Cosmetics Formulations:
POE (20) ISOHEXADECYL ETHER is used as an oil in water (O/W) emulsifier for creams and lotions, as well as a wetting agent.

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 9004-95-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 9,0,0 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 9004-95:
(6*9)+(5*0)+(4*0)+(3*4)+(2*9)+(1*5)=89
89 % 10 = 9
So 9004-95-9 is a valid CAS Registry Number.

9004-95-9 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • USP

  • (1547801)  Polyoxyl 20 cetostearyl ether  United States Pharmacopeia (USP) Reference Standard

  • 9004-95-9

  • 1547801-100MG

  • 4,662.45CNY

  • Detail
  • Aldrich

  • (388831)  Brij® 52  average Mn ~330

  • 9004-95-9

  • 388831-100G

  • 434.07CNY

  • Detail
  • Sigma

  • (P5884)  Brij® 58  average Mn ~1124

  • 9004-95-9

  • P5884-100G

  • 432.90CNY

  • Detail
  • Sigma

  • (P5884)  Brij® 58  average Mn ~1124

  • 9004-95-9

  • P5884-500G

  • 712.53CNY

  • Detail
  • Sigma

  • (P5884)  Brij® 58  average Mn ~1124

  • 9004-95-9

  • P5884-1KG

  • 1,578.33CNY

  • Detail
  • Aldrich

  • (388858)  Brij® C10  average Mn ~683

  • 9004-95-9

  • 388858-100G

  • 411.84CNY

  • Detail
  • Aldrich

  • (388858)  Brij® C10  average Mn ~683

  • 9004-95-9

  • 388858-1KG

  • 1,404.00CNY

  • Detail

9004-95-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name POE (20) ISOHEXADECYL ETHER

1.2 Other means of identification

Product number -
Other names 2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-hexadecoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol

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:9004-95-9 SDS

9004-95-9Downstream Products

9004-95-9Relevant articles and documents

Liposome Enhanced Detection of Amyloid Protein Aggregates

Kocsis, Istvan,Sanna, Elena,Hunter, Christopher A.

, p. 647 - 650 (2021/02/06)

Thioflavin-T is used to image amyloid aggregates because of the excellent turn-on fluorescence properties, but binding affinities are low. By mounting multiple dye units on the surface of a vesicle, the binding affinity for α-synuclein fibrils is increased by three orders of magnitude, and the optical response is increased. Cooperative interactions of the dye headgroup and lipid with the protein provide a general strategy for the construction of multivalent amyloid probes based on vesicles.

Polycyclic pyridinone compounds and pharmaceutical compositions and uses thereof

-

Paragraph 0181-0186, (2021/11/06)

The invention discloses a polycyclic pyridone compound as well as a pharmaceutical composition and application thereof, and the polycyclic pyridone compound is shown as a formula (I). The compound can be used for preparing anti-virus infection drugs.

Preparation method of higher fatty alcohol 2-alkoxy ethanol

-

Paragraph 0030; 0043; 0045-0048, (2021/08/25)

The invention provides a preparation method of higher fatty alcohol 2-alkoxy ethanol, and relates to the technical field of organic synthesis, higher fatty alcohol and sulfonyl halide are used as raw materials for cascade reaction, the higher fatty alcohol is completely converted into sulfonate under the action of alkali, and then the sulfonate is subjected to phase transfer reaction under the promotion of a phase transfer catalyst (the used phase transfer catalyst comprises quaternary ammonium salt or crown ether), sulfonate directly performs nucleophilic substitution reaction with ethylene glycol, and the reaction temperature is controlled to complete the reaction within half an hour to obtain the corresponding higher fatty alcohol 2-alkoxy ethanol. The method is low in raw material and reagent cost, simple in process operation, small in pollution, high in product yield and purity, and suitable for large-scale preparation.

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