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Nitroterephthalic acid

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Nitroterephthalic acid Basic information

Product Name:
Nitroterephthalic acid
Synonyms:
  • NITROTEREPHTHALIC ACID
  • 2-nitro-4-benzenedicarboxylicacid
  • 2-NITROBENZENE-1,4-DIOIC ACID
  • 2-NITROTEREPHTHALIC ACID
  • 2-NITRO-1,4-DIBENZOIC ACID
  • 2-Nitrobenzene-1,4-dicarboxylic acid
  • NITROTEREPHTHALIC ACID, 99+%
  • NITROTEREPHTHALIC ACID2-NITRO-1,4-DIBENZOIC ACID
CAS:
610-29-7
MF:
C8H5NO6
MW:
211.13
EINECS:
210-217-4
Product Categories:
  • Building Blocks
  • Carbonyl Compounds
  • Carboxylic Acids
  • Chemical Synthesis
  • Organic Building Blocks
  • C8
  • Carbonyl Compounds
  • Carboxylic Acids
  • Phthalic Acids, Esters and Derivatives
  • Derivatives of phthalic acid
  • 610-29-7
Mol File:
610-29-7.mol
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Nitroterephthalic acid Chemical Properties

Melting point:
270-272 °C (lit.)
Boiling point:
350.79°C (rough estimate)
Density 
1.6342 (rough estimate)
refractive index 
1.5282 (estimate)
storage temp. 
Sealed in dry,Room Temperature
solubility 
almost transparency in Methanol
pka
pK1:1.73 (25°C)
form 
Powder
color 
White to light beige
BRN 
1913836
InChI
InChI=1S/C8H5NO6/c10-7(11)4-1-2-5(8(12)13)6(3-4)9(14)15/h1-3H,(H,10,11)(H,12,13)
InChIKey
QUMITRDILMWWBC-UHFFFAOYSA-N
SMILES
C1(C(O)=O)=CC=C(C(O)=O)C=C1[N+]([O-])=O
CAS DataBase Reference
610-29-7(CAS DataBase Reference)
EPA Substance Registry System
2-Nitroterephthalic acid (610-29-7)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-37/39
WGK Germany 
3
TSCA 
Yes
HS Code 
29173990

MSDS

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Nitroterephthalic acid Usage And Synthesis

Chemical Properties

white crystalline powder

Synthesis

100-21-0

610-29-7

The general procedure for synthesizing 2-nitroterephthalic acid from terephthalic acid (PTA) is as follows: 1 wt. part of PTA is mixed with 8 wt. parts of concentrated sulfuric acid at a concentration of 82% at 5°C, and 1 wt. part of 66% concentrated nitric acid is slowly added. The reaction mixture was heated to 60°C and maintained for 1 hour. Upon completion of the reaction, it was cooled to room temperature and vacuum filtered. The filter cake was mixed well with deionized water and heated to 80°C for 10 hours of reaction. The vacuum filtration operation was repeated until the filtrate was recrystallized in ice water. After filtration, the filtrate was dried under vacuum at 60 °C for 2 h to obtain 2-nitro terephthalic acid (PTANitro compound) with 93% purity and 68.6% yield.

References

[1] RSC Advances, 2016, vol. 6, # 10, p. 8495 - 8502
[2] Patent: CN103664684, 2016, B. Location in patent: Paragraph 0038
[3] Monatshefte fuer Chemie, 1886, vol. 7, p. 140
[4] Chemische Berichte, 1877, vol. 10, p. 145
[5] Justus Liebigs Annalen der Chemie, 1862, vol. 121, p. 90

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