Nitroterephthalic acid
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
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)
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
- Language:English Provider:2-Nitroterephthalic acid
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
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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Nitroterephthalic acid(610-29-7)Related Product Information
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- Dimethyl terephthalate
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- Citric acid
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- NITROTEREPHTHALIC ACID DIMETHYL ESTER
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- 2-Nitroterephthalic acid 4-methyl ester, 97%
- 2-Nitro-1,4-benzenedicarboxylic acid dimethyl ester
- Formic acid
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