Home Amines 5434-21-9
5434-21-9,MFCD00013985
Catalog No.:AA003KP5

5434-21-9 | 4-Aminophthalic acid

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1g
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5g
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25g
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  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003KP5
Chemical Name:
4-Aminophthalic acid
CAS Number:
5434-21-9
Molecular Formula:
C8H7NO4
Molecular Weight:
181.1455
MDL Number:
MFCD00013985
SMILES:
Nc1ccc(c(c1)C(=O)O)C(=O)O
NSC Number:
15742
Properties
Properties
 
BP:
465.1°C at 760 mmHg  
Form:
Solid  
MP:
344 °C (dec.)(lit.)  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
228  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
2  
XLogP3:
0.7  

Upstream Synthesis Route

[1]KogyoKagakuZasshi,Spl.44<1941>450,

[2]Chem.Abstr.,1951,p.1544

[3]KogyoKagakuZasshi,1941,vol.44,p.1025

[1]Patent:US6689922,2004,B1,.Locationinpatent:Pagecolumn20

[2]Patent:US6706725,2004,B1,.Locationinpatent:Pagecolumn11

[3]ChemicalCommunications,2017,vol.53,#62,p.8751-8754

[4]JustusLiebigsAnnalenderChemie,1881,vol.208,p.230

[5]JournaloftheAmericanChemicalSociety,1908,vol.30,p.1143

[6]ZhurnalRusskagoFiziko-KhimicheskagoObshchestva,1878,vol.10,p.192

[7]JustusLiebigsAnnalenderChemie,1881,vol.208,p.225

[8]ChemischeBerichte,1901,vol.34,p.4352

[9]JustusLiebigsAnnalenderChemie,1881,vol.208,p.230

[10]JournaloftheAmericanChemicalSociety,1908,vol.30,p.1143

[11]ZhurnalRusskagoFiziko-KhimicheskagoObshchestva,1878,vol.10,p.192

[12]JustusLiebigsAnnalenderChemie,1881,vol.208,p.225

[13]Journalofmedicinalchemistry,1966,vol.9,#1,p.165-168

[14]LettersinDrugDesignandDiscovery,2013,vol.10,#9,p.872-878

[1]EuropeanJournalofOrganicChemistry,2014,vol.2014,#12,p.2443-2450

[1]JournaloftheAmericanChemicalSociety,1908,vol.30,p.1143

[2]JournaloftheAmericanChemicalSociety,1906,vol.28,p.618

[1]ZhurnalRusskagoFiziko-KhimicheskagoObshchestva,1878,vol.10,p.192

[2]JustusLiebigsAnnalenderChemie,1881,vol.208,p.225

[3]JustusLiebigsAnnalenderChemie,1881,vol.208,p.230

Downstream Synthesis Route

[1]Patent:US6689922,2004,B1.Locationinpatent:Pagecolumn20

[2]Patent:US6706725,2004,B1.Locationinpatent:Pagecolumn11

[3]ChemicalCommunications,2017,vol.53,p.8751-8754

[4]JustusLiebigsAnnalenderChemie,1881,vol.208,p.230

[5]ChemischeBerichte,1901,vol.34,p.4352

[6]JustusLiebigsAnnalenderChemie,1881,vol.208,p.230

[7]Journalofmedicinalchemistry,1966,vol.9,p.165-168

[8]Lettersindrugdesignanddiscovery,2013,vol.10,p.872-878

[1]JournaloftheAmericanChemicalSociety,1908,vol.30,p.1143

[1]JournaloftheAmericanChemicalSociety,1908,vol.30,p.1143

[1]KogyoKagakuzasshi/JournaloftheSocietyofChemicalIndustry,Spl.44<1941>450,    Chem.Abstr.,1951,p.1544

[1]JournaloftheAmericanChemicalSociety,1908,vol.30,p.1143

Literature

Title: Immune enhancement by novel vaccine adjuvants in autoimmune-prone NZB/W F1 mice: relative efficacy and safety.

Journal: BMC immunology 20110101

Title: An indirect competitive fluorescence immunoassay for determination of dicyclohexyl phthalate in water samples.

Journal: Journal of fluorescence 20101101

Title: [Study of dicyclohexyl phthalate on preparation and characterization of artificial antigen].

Journal: Wei sheng yan jiu = Journal of hygiene research 20060901

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SDS
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