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537-98-4 Usage

Chemical Properties



Different sources of media describe the Uses of 537-98-4 differently. You can refer to the following data:
1. trans-Ferulic acid was used for esterification of methacrylated dextran. It was also used to study the effect of oral administration of trans-ferulic acid to c57BL mice on ethanol-induced liver injury. Furthermore, it has been used in the synthesis of new biocompatible antioxidant polymers linking trans-ferulic acid.
2. These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.

Biochem/physiol Actions

Hydroxycinnamic acid found in plant-based foods. Antioxidant.

Check Digit Verification of cas no

The CAS Registry Mumber 537-98-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,3 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 537-98:
84 % 10 = 4
So 537-98-4 is a valid CAS Registry Number.

537-98-4 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (H0267)  trans-Ferulic Acid  >98.0%(GC)(T)

  • 537-98-4

  • 25g

  • 570.00CNY

  • Detail
  • TCI America

  • (H0267)  trans-Ferulic Acid  >98.0%(GC)(T)

  • 537-98-4

  • 250g

  • 2,990.00CNY

  • Detail
  • Alfa Aesar

  • (A13890)  trans-4-Hydroxy-3-methoxycinnamic acid, 99%   

  • 537-98-4

  • 25g

  • 372.0CNY

  • Detail
  • Alfa Aesar

  • (A13890)  trans-4-Hydroxy-3-methoxycinnamic acid, 99%   

  • 537-98-4

  • 100g

  • 1163.0CNY

  • Detail
  • Alfa Aesar

  • (A13890)  trans-4-Hydroxy-3-methoxycinnamic acid, 99%   

  • 537-98-4

  • 500g

  • 4731.0CNY

  • Detail
  • Sigma-Aldrich

  • (52229)  trans-Ferulic acid  certified reference material, TraceCERT®

  • 537-98-4

  • 52229-50MG

  • 1,075.23CNY

  • Detail
  • Sigma-Aldrich

  • (Y0001013)  Ferulic acid  European Pharmacopoeia (EP) Reference Standard

  • 537-98-4

  • Y0001013

  • 1,880.19CNY

  • Detail



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


1.1 GHS Product identifier

Product name Trans-Ferulic Acid

1.2 Other means of identification

Product number -
Other names trans-Ferulic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:537-98-4 SDS

537-98-4Relevant articles and documents

Photoinduced Regioselective Olefination of Arenes at Proximal and Distal Sites

Ali, Wajid,Anjana, S. S.,Bhattacharya, Trisha,Chandrashekar, Hediyala B.,Goswami, Nupur,Guin, Srimanta,Maiti, Debabrata,Panda, Sanjib,Prakash, Gaurav,Saha, Argha,Sasmal, Sheuli,Sinha, Soumya Kumar

, p. 1929 - 1940 (2022/02/01)

The Fujiwara-Moritani reaction has had a profound contribution in the emergence of contemporary C-H activation protocols. Despite the applicability of the traditional approach in different fields, the associated reactivity and regioselectivity issues had

First total syntheses of four natural bioactive glucosides

Xu, Guangya,Wu, Min,Yao, Zhongquan,Lou, Hongbin,Du, Weihong,Song, Mingwei,He, Yujiao,Dong, Hongbo

supporting information, p. 1266 - 1271 (2021/02/06)

The efficient total syntheses of four biologically interesting natural glucosides Ethylconiferin, Butylconiferin, 2’-Butoxyethylconiferin and Balajaponin B, have been achieved for the first time starting from commercially available Vanilline via concise reaction sequence of 8–10 steps with the overall yield of 26–41%. This work definitely laid the foundation for the further pharmacological study of this kind of natural compounds. Meanwhile, currently developed approach could be used as a general synthetic strategy for the syntheses of other monolignol glucosides and their derivatives, and provides an opportunity for further study of the structure-activity relationship of this kind of glucosides.

A Thorough Study on the Photoisomerization of Ferulic Acid Derivatives

Moni, Lisa,Banfi, Luca,Basso, Andrea,Mori, Alessia,Risso, Federica,Riva, Renata,Lambruschini, Chiara

supporting information, p. 1737 - 1749 (2021/03/23)

A thorough study on the (E) to (Z) photoisomerization of ferulic acid derivatives (esters, amides of all types, and ketones) was carried out. At the photostationary state, only aliphatic or benzylic tertiary amides reach a nearly complete conversion of (E) isomers into the (Z) ones, whereas for esters, primary and secondary amides or aromatic tertiary amides mixtures of (Z)/(E) ranging from 7 : 93 to 72 : 28 are observed. Ketones show rather limited photoisomerization. However, (Z) ketones may be obtained by the reaction of organometal compounds with an isomerized (Z) Weinreb amide.

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