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Sodium 1,1,2,3,3,3-hexafluoro-propane-1-sulfonate, also known as sodium hexafluoropropene sulfonate or NaHF6PS, is a synthetic chemical compound with the molecular formula C3HF6NaO3S. It is a colorless, odorless, and water-soluble solid, often used as a salting agent in various applications. SODIUM 1,1,2,3,3,3-HEXAFLUORO-PROPANE-1-SULFONATE is derived from hexafluoropropene, a fluorinated hydrocarbon, and exhibits unique properties due to its fluorinated structure. Sodium hexafluoropentane-1-sulfonate is known for its high thermal stability, low toxicity, and excellent solubility in water, making it suitable for use in various industrial processes, including as a component in electrolytes for batteries and as a stabilizer in chemical reactions.

3916-24-3

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3916-24-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3916-24-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,1 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3916-24:
(6*3)+(5*9)+(4*1)+(3*6)+(2*2)+(1*4)=93
93 % 10 = 3
So 3916-24-3 is a valid CAS Registry Number.

3916-24-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium,1,1,2,3,3,3-hexafluoropropane-1-sulfonate

1.2 Other means of identification

Product number -
Other names SODIUM 1,1,2,3,3,3-HEXAFLUOROPROPANESULFONATE

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:3916-24-3 SDS

3916-24-3Upstream product

3916-24-3Relevant academic research and scientific papers

PROCESSES FOR MAKING DIALKYL ETHERS FROM ALCOHOLS

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Page/Page column 31-32, (2009/04/25)

Processes for the preparation of dialkyl ethers from C4 to C8 straight-chain alcohols using an ionic liquid.

PROCESSES FOR MAKING DIBUTYL ETHERS FROM ISOBUTANOL

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Page/Page column 31-32, (2009/04/25)

Processes for preparing dibutyl ethers from isobutanol using an ionic liquid.

PROCESSES FOR MAKING DIALKYL ETHERS FROM ALCOHOLS

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Page/Page column 21-22, (2009/04/25)

Processes for preparing dialkyl ethers from C4 to C8 straight-chain alcohols using an ionic liquid.

PROCESSES FOR MAKING DIBUTYL ETHERS FROM 2-BUTANOL

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Page/Page column 21-22, (2009/04/25)

Processes for preparing dibutyl ethers from 2-butanol using an ionic liquid.

PROCESSES FOR MAKING DIBUTYL ETHERS FROM ISOBUTANOL

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Page/Page column 21-22, (2009/04/25)

Processes for preparing dibutyl ethers from isobutanol using an ionic liquid.

PROCESSES FOR MAKING DIBUTYL ETHERS FROM 2-BUTANOL

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Page/Page column 31-32, (2009/04/25)

Processes for preparing dibutyl ethers from 2-butanol using an ionic liquid.

Preparation of poly(tetramethylene) glycol

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Page/Page column 7, (2008/06/13)

This invention relates to a process comprising using ionic liquids for preparing poly(tetramethylene) glycol from tetrahydrofuran.

Alkylation of aromatic compounds

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Page/Page column 6, (2008/06/13)

The present invention relates to the synthesis of alkylated aromatic compounds. Alkylated aromatic compounds are synthesized by reacting an aromatic compound with a monoolefin in the presence of a porous microcomposite comprising at least one fluorinated sulfonic acid on silica.

Ionic liquids

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Page/Page column 7, (2008/06/13)

Compositions of matter useful as ionic liquids of the formula Z+A?, wherein Z+ is a cation selected from the group consisting of pyridinium, pyridazinium, pyrimidinium, pyrazinium, imidazolium, pyrazolium, thiazolium, oxazolium, triazolium, and phosphonium, ammonium cations with specified substituents, and A? is selected from the group consisting of the following three anions wherein R11, R12 and R13 are as specified. R11—CHF—CF2—SO3???Formula I R12—CF2—CF2—SO3???Formula II (R13—CHF—CF2—SO2)2N???Formula III

Ionic liquids

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Page/Page column 7, (2008/06/13)

The present invention relates to compositions of matter that are useful as ionic liquids. The compositions of the invention are based on an N-substituted pyrrolidinone, said pyrrolidinone having a pendant ammonium cation that is separated from the pyrrolidone ring by a variable length alkyl spacer. The compositions comprise fluoroalkyl sulfonate anions.

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