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Nitroterephthalic acid

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CAS:610-29-7
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CAS:610-29-7
Purity:99% Package:1kg

Nitroterephthalic acid manufacturers

Nitroterephthalic acid Basic information
Product Name:Nitroterephthalic acid
Synonyms:NITROTEREPHTHALIC ACID;2-nitro-4-benzenedicarboxylicacid;2-NITROBENZENE-1,4-DIOIC ACID;2-NITRO-1,4-DIBENZOIC ACID;2-Nitrobenzene-1,4-dicarboxylic acid;NITROTEREPHTHALIC ACID, 99+%;NITROTEREPHTHALIC ACID2-NITRO-1,4-DIBENZOIC ACID;NitroterephthaL
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 Structure
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
pkapK1:1.73 (25°C)
form Powder
color White to light beige
BRN 1913836
InChIInChI=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)
InChIKeyQUMITRDILMWWBC-UHFFFAOYSA-N
SMILESC1(C(O)=O)=CC=C(C(O)=O)C=C1[N+]([O-])=O
CAS DataBase Reference610-29-7(CAS DataBase Reference)
EPA Substance Registry System2-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 TSCA listed
HS Code 29173990
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
2-Nitroterephthalic acid English
ACROS English
SigmaAldrich English
ALFA English
Nitroterephthalic acid Usage And Synthesis
Chemical Propertieswhite crystalline powder
Synthesis
Terephthalic acid

100-21-0

Nitroterephthalic acid

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
Nitroterephthalic acid Preparation Products And Raw materials
Raw materialsTerephthalic acid
Preparation Productsdiethyl 2-nitroterephthalate-->2-AMINOTEREPHTHALIC ACID-->AKOS B007547
Tag:Nitroterephthalic acid(610-29-7) Related Product Information
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