1137-73-1

Basic information

• Product Name: N-PHENYLIMINODIACETIC ACID
• Synonyms: Acetic acid,1-phenyliminodi-;anilinediaceticacid;Glycine, N-(carboxymethyl)-N-phenyl-;Glycine,N-(carboxymethyl)-N-phenyl-;phenylimino-di-aceticacid;N-PHENYLIMINODIACETIC ACID;N,N-ANILINEDIACETIC ACID;N,N-DI(CARBOXYMETHYL)ANILINE
• CAS NO: 1137-73-1
• Molecular Formula: C₁₀H₁₁NO₄
• Molecular Weight: 209.2
• Mol File: 1137-73-1.mol
• Article Data: 6

Chemical Properties

• Melting Point: 156 °C
• Boiling Point: 451.2 °C at 760 mmHg
• Flash Point: 226.7 °C
• Appearance: Grayish to beige/Powder
• Density: 1.397 g/cm³
• Vapor Pressure: 6.25E-09mmHg at 25°C
• PKA: pK1:2.40;pK2:4.98 (20°C)
• BRN: 2808435
• CAS DataBase Reference: N-PHENYLIMINODIACETIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: N-PHENYLIMINODIACETIC ACID(1137-73-1)
• EPA Substance Registry System: N-PHENYLIMINODIACETIC ACID(1137-73-1)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36
• Hazardous Substances Data: 1137-73-1(Hazardous Substances Data)

Usage

Chemical Properties

Greyish to beige powder

InChI:InChI=1/C10H11NO4/c12-9(13)6-11(7-10(14)15)8-4-2-1-3-5-8/h1-5H,6-7H2,(H,12,13)(H,14,15)/p-2

Upstream product

• 103-01-5 N-Phenylglycine 
• 79-11-8 chloroacetic acid 
• 3926-62-3 sodium monochloroacetic acid 
• 55932-12-2 phenyliminodiacetic acid diethyl ester 
• 7732-18-5 water 
• 62-53-3 aniline 
• 127-09-3 sodium acetate 
• 120-07-0 2,2'-(phenylimino)bis[ethanol] 

Downstream Products

• 93136-36-8 N-(methoxycarbonylmethyl)-N-phenylglycine methyl ester 
• 55932-12-2 phenyliminodiacetic acid diethyl ester 
• 56956-66-2 4-phenylmorpholine-2,6-dione 
• 78158-74-4 formanilinoacetic acid 
• 121-69-7 N,N-dimethyl-aniline 
• 743422-98-2 N-phenyl-N-(phenylcarbamoyl-methyl)-glycine 
• 13480-19-8 1-benzyl-4-phenyl-piperazine-2,6-dione 
• 50794-23-5 o-formylphenylglycine 
• 161555-27-7 (Methoxycarbonylmethyl-phenyl-amino)-acetic acid 
• 161555-23-3 [(2-Ethoxymethoxy-ethyl)-phenyl-amino]-acetic acid methyl ester 
• 30810-75-4 1,4-diphenyl-piperazine-2,6-dione 
• 99168-31-7 phenylimino-di-acetic acid diamide 

Relevant articles and documents

Deep eutectic solvent-based ligandless ultrasound-assisted liquid-phase microextraction for extraction of cobalt ions from food samples prior to spectrophotometric determination

An innovative environmentally friendly deep eutectic solvent-based ligandless ultrasound-assisted liquid-phase microextraction was introduced for spectrophotometric determination of trace amount of cobalt. n-phenyliminodiacetic acid: choline chloride (2:1?mol ratio) as a novel DES was prepared for extraction of cobalt ions which is both as chelating agent and extraction solvent. The pivotal factors affecting the proposed method including pH, time, temperature, extraction solvent volume, ionic strength, and sample volume were investigated. At optimum conditions, limit of detection and limit of quantification of 5.23?μg?L?1 and 17.67?μg?L?1 were achieved respectively. The linear range of 20–200?μg?L?1 and precision (relative standard deviation %) of 3.4 for 100?μg?L?1 Co+2 solution were gained. The proposed method was successfully applied in water samples, tomato sauce, black and green tea, and dark chocolate with high recovery values (%) of 94–105.

Tunable excitation-dependent emissions in mixed-ligand Cd(II) complexes

Two Cd(II) coordination compounds, i.e. [Cd(HL)(phen)2(H2O)]·HL·3H2O (1) and {[Cd(HMeL)2(4,4′-bipy)(H2O)]·H2O}n (2) and (where HL = N-carboxymethyl-N-phenyliminoacetato, HMeL = N

SYNTHESIS OF BAPTA-AM ANALOGUES CAPABLE OF ENHANCING THE VASCULAR PRODUCTION OF PROSTACYCLIN

About 30 analogues of BAPTA-AM, a potential antithrombotic agent, have been synthesized and tested for their effect on the production of prostacyclin.None of them was found to be a better enhancher of the production of prostacyclin by aortic endothelial cells than BAPTA-AM itself.The enhancing effect can be produced by compounds unable to chelate Ca2+, thus confirming that it is not related to their buffering capacity for free Ca2+.