94-53-1

  • Product Name:Piperonylic acid
  • Molecular Formula:C8H6O4
  • Purity:99%
  • Molecular Weight:166.133
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Product Details;

CasNo: 94-53-1

Molecular Formula: C8H6O4

Appearance: white to light yellow crystal powder

Factory Supply Wholesale Piperonylic acid 94-53-1 Best Price

  • Molecular Formula:C8H6O4
  • Molecular Weight:166.133
  • Appearance/Colour:white to light yellow crystal powder 
  • Vapor Pressure:9.95E-05mmHg at 25°C 
  • Melting Point:229-231 °C(lit.) 
  • Refractive Index:1.612 
  • Boiling Point:324.6 °C at 760 mmHg 
  • PKA:4.35±0.20(Predicted) 
  • Flash Point:139.6 °C 
  • PSA:55.76000 
  • Density:1.468 g/cm3 
  • LogP:1.11350 

Piperonylic acid(Cas 94-53-1) Usage

Chemical Properties

white to light yellow crystal powde

Uses

Piperonylic Acid is a compound closely mimicking the structure of transcinnamic acid involved in the phenylpropanoid pathway in plant physiology.

Synthesis Reference(s)

The Journal of Organic Chemistry, 40, p. 3803, 1975 DOI: 10.1021/jo00913a051

Purification Methods

Crystallise the acid from EtOH or water. [Beilstein 19/7 V 300.]

InChI:InChI=1/C8H6O4/c9-8(10)5-1-2-6-7(3-5)12-4-11-6/h1-3H,4H2,(H,9,10)

94-53-1 Relevant articles

Piperonylic Acid, a Selective, Mechanism-Based Inactivator of the trans-Cinnamate 4-Hydroxylase: A New Tool to Control the Flux of Metabolites in the Phenylpropanoid Pathway

Michel Schalk, Francisco Cabello-Hurtado, Marie-Agnès Pierrel, Rossitza Atanassova, Patrick Saindrenan, Danièle Werck-Reichhart

, Plant Physiology, Volume 118, Issue 1, September 1998, Pages 209–218,

Piperonylic acid (PA) is a natural molecule bearing a methylenedioxy function that closely mimics the structure of trans-cinnamic acid. The CYP73A subfamily of plant P450s catalyzes trans-cinnamic acid 4-hydroxylation, the second step of the general phenylpropanoid pathway.

Destructible Surfactants Based on a Silicon-Oxygen Bond

Jaeger, David A.,Ward, Mary Darlene

, p. 2221 - 2223 (1982)

A "destructible" surfactant based on the...

Gram-scale synthesis of carboxylic acids via catalytic acceptorless dehydrogenative coupling of alcohols and hydroxides at an ultralow Ru loading

Chen, Cheng,Cheng, Hua,Verpoort, Francis,Wang, Zhi-Qin,Wu, Zhe,Yuan, Ye,Zheng, Zhong-Hui

, (2021/12/13)

Acceptorless dehydrogenative coupling (A...

Oxidation of Primary Alcohols and Aldehydes to Carboxylic Acids via Hydrogen Atom Transfer

Tan, Wen-Yun,Lu, Yi,Zhao, Jing-Feng,Chen, Wen,Zhang, Hongbin

supporting information, p. 6648 - 6653 (2021/09/08)

The oxidation of primary alcohols and al...

Ni-NiO heterojunctions: a versatile nanocatalyst for regioselective halogenation and oxidative esterification of aromatics

Bhardwaj, Nivedita,Goel, Bharat,Indra, Arindam,Jain, Shreyans K.,Singh, Ajit Kumar,Tripathi, Nancy

, p. 14177 - 14183 (2021/08/16)

Herein, we report a facile method for th...

One-Pot Direct Oxidation of Primary Amines to Carboxylic Acids through Tandem ortho-Naphthoquinone-Catalyzed and TBHP-Promoted Oxidation Sequence

Kim, Hun Young,Oh, Kyungsoo,Si, Tengda

supporting information, p. 18150 - 18155 (2021/12/09)

Biomimetic oxidation of primary amines t...

94-53-1 Process route

furan-2,3,5(4H)-trione pyridine (1:1)

furan-2,3,5(4H)-trione pyridine (1:1)

piperonal-((<i>E</i>)-<i>O</i>-[1]naphthylcarbamoyl oxime )

piperonal-((E)-O-[1]naphthylcarbamoyl oxime )

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Conditions
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Conditions
Conditions Yield
at 3 ℃;
 

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