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Phosphonium, (4-iodobutyl)triphenyl-, iodide is a chemical compound that features a phosphonium cation paired with an iodide anion. Phosphonium, (4-iodobutyl)triphenyl-, iodide is characterized by a triphenylphosphonium group, which acts as a lipophilic anchor, enhancing solubility in organic solvents and enabling the transfer of reactants between aqueous and organic phases. The 4-iodobutyl substituent contributes additional reactivity and selectivity, making Phosphonium, (4-iodobutyl)triphenyl-, iodide a versatile catalyst in various chemical processes.

159085-21-9

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159085-21-9 Usage

Uses

Used in Organic Synthesis:
Phosphonium, (4-iodobutyl)triphenyl-, iodide is utilized as a phase-transfer catalyst in organic reactions, facilitating the synthesis of complex organic molecules by promoting the transfer of reactants between different phases.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, Phosphonium, (4-iodobutyl)triphenyl-, iodide is employed as a catalyst to aid in the production of various drugs, leveraging its ability to simplify the synthesis of intricate organic molecules, which is crucial for the development of new medications.
Used in Agrochemical Production:
Phosphonium, (4-iodobutyl)triphenyl-, iodide also finds application in the agrochemical sector, where it serves as a catalyst in the synthesis of pesticides and other agricultural chemicals, contributing to the efficiency and selectivity of the production processes.
Used in Fine Chemicals Industry:
Phosphonium, (4-iodobutyl)triphenyl-, iodide is used in the synthesis of fine chemicals, where its unique structural features and catalytic properties are valuable for the production of high-purity specialty chemicals required in various applications.
Used in Chemical Research:
Due to its unique structural features and catalytic capabilities, Phosphonium, (4-iodobutyl)triphenyl-, iodide is a valuable tool in chemical research, enabling scientists to explore new reaction pathways and develop innovative synthetic methods.

Check Digit Verification of cas no

The CAS Registry Mumber 159085-21-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,0,8 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 159085-21:
(8*1)+(7*5)+(6*9)+(5*0)+(4*8)+(3*5)+(2*2)+(1*1)=149
149 % 10 = 9
So 159085-21-9 is a valid CAS Registry Number.

159085-21-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-iodobutyl(triphenyl)phosphanium,iodide

1.2 Other means of identification

Product number -
Other names Phosphonium,(4-iodobutyl)triphenyl-,iodide

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:159085-21-9 SDS

159085-21-9Downstream Products

159085-21-9Relevant academic research and scientific papers

Tandem mass spectrometric characterization of thiol peptides modified by the chemoselective cationic sulfhydryl reagent (4-iodobutyl) triphenylphosphonium - Effects of a cationic thiol derivatization on peptide fragmentation

Wang, Jing,Zhang, Jie,Arbogast, Brian,Maier, Claudia S.

, p. 1771 - 1783 (2011)

Fixed charge chemical modifications on peptides and proteins can impact fragmentation behaviors in tandem mass spectrometry (MS/MS). In this study, we employed a thiol-specific cationic alkylation reagent, (4-iodobutyl) triphenylphosphonium (IBTP), to sel

Monitoring and Modulating mtDNA G-Quadruplex Dynamics Reveal Its Close Relationship to Cell Glycolysis

Chen, Shuo-Bin,Chen, Xiu-Cai,Dai, Jing,Huang, Zhi-Shu,Luo, Wen-Hua,Shao, Wen,Tan, Jia-Heng,Tang, Gui-Xue,Zeng, Shu-Tang

supporting information, p. 20779 - 20791 (2021/12/14)

The mitochondrial DNA G-quadruplex (mtDNA G4) is a potential regulatory element for the regulation of mitochondrial functions; however, its relevance and specific roles in diseases remain largely unknown. Here, we engineered a set of chemical probes, incl

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