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1197-55-3

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1197-55-3 Usage

Chemical Properties

light yellow to beige powder

Uses

Different sources of media describe the Uses of 1197-55-3 differently. You can refer to the following data:
1. It is a non-translocated competitive inhibitor of the epithelial peptide transporter PepT1
2. 4-Aminophenylacetic acid, is used as a non-translocated competitive inhibitor of the epithelial peptide transporter PepT1. It can be detected using HPLC, NMR techniques.

Purification Methods

Crystallise the acid from hot water (60-70mL/g). [Beilstein 14 III 1182.]

Check Digit Verification of cas no

The CAS Registry Mumber 1197-55-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,9 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1197-55:
(6*1)+(5*1)+(4*9)+(3*7)+(2*5)+(1*5)=83
83 % 10 = 3
So 1197-55-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H9NO2/c9-7-3-1-6(2-4-7)5-8(10)11/h1-4H,5,9H2,(H,10,11)/p-1

1197-55-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (A14675)  4-Aminophenylacetic acid, 98%   

  • 1197-55-3

  • 10g

  • 370.0CNY

  • Detail
  • Alfa Aesar

  • (A14675)  4-Aminophenylacetic acid, 98%   

  • 1197-55-3

  • 50g

  • 1343.0CNY

  • Detail
  • Alfa Aesar

  • (A14675)  4-Aminophenylacetic acid, 98%   

  • 1197-55-3

  • 250g

  • 3712.0CNY

  • Detail
  • Aldrich

  • (A71352)  4-Aminophenylaceticacid  98%

  • 1197-55-3

  • A71352-25G

  • 355.68CNY

  • Detail
  • Aldrich

  • (A71352)  4-Aminophenylaceticacid  98%

  • 1197-55-3

  • A71352-100G

  • 1,182.87CNY

  • Detail
  • Vetec

  • (V900585)  4-Aminophenylaceticacid  Vetec reagent grade, 98%

  • 1197-55-3

  • V900585-10G

  • 294.04CNY

  • Detail
  • Vetec

  • (V900585)  4-Aminophenylaceticacid  Vetec reagent grade, 98%

  • 1197-55-3

  • V900585-50G

  • 1,119.54CNY

  • Detail

1197-55-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Aminophenylacetic acid

1.2 Other means of identification

Product number -
Other names (4-AMINO-PHENYL)-ACETIC ACID

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:1197-55-3 SDS

1197-55-3Relevant articles and documents

-

Dippy,Williams

, p. 161,164 (1934)

-

A method for preparing the amino acetic acid (by machine translation)

-

Paragraph 0017; 0023; 0024, (2017/01/19)

The invention discloses a method for preparing the amino acetic acid, comprises the following steps: the water, ferric chloride, acetic acid mix to the nitrobenzene, in under the nitrogen atmosphere up to 60 - 90 °C, water drop [...] aqueous solution, thermal insulation 1 - 2h, the temperature crystallization, filter and filter cake, washing, drying to obtain the amino acetic acid. This invention does not produce difficult to dispose of solid waste, is free of organic solvent, the protection of the environment, mild reaction conditions, the operation is simple, and is suitable for industrial production, high yield, preparation to get amino acetic acid purity is good, for the normal and stable production of the acher he benefits help. (by machine translation)

Immunomodulatory peptides

-

, (2014/12/12)

The invention relates to peptides derivatized with a hydrophilic polymer which, in some embodiments, bind to human FcRn and inhibit binding of the Fc portion of an IgG to an FcRn, thereby modulating serum IgG levels. The disclosed compositions and methods may be used in some embodiments, for example, in treating autoimmune diseases and inflammatory disorders. The invention also relates, in further embodiments, to methods of using and methods of making the peptides of the invention.

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