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618-88-2

618-88-2 Structure

618-88-2 Structure
IdentificationMore
[Name]

5-Nitroisophthalic acid
[CAS]

618-88-2
[Synonyms]

3-NITRO-5-CARBOXYLIC ACID BENZOIC ACID
5-nitro-1,3-benzenedicarboxylic acid
5-NITROBENZENE-1,3-DICARBOXYLIC ACID
5-NITROISOPHTHALIC ACID
NITROISOPHTHALIC-5 ACID
NITRO ISOPHTHALIC ACID
5-nitro-3-benzenedicarboxylicacid
5-NIPA
5-NITRO-ISO-PHTHALIC ACID PESTANAL
5itroIsophathalicAcid
1,3-BENZENEDICARBOXYLIC ACID,5-NITRO
5-NITROISOPHTHALIC ACID 99+%
5-NITROISOPHTHALIC ACID5-NITRO-PHENYL-1,3-DICARBOXYLIC ACID
5-Nitro-m-phthalic acid
[EINECS(EC#)]

210-568-3
[Molecular Formula]

C8H5NO6
[MDL Number]

MFCD00007254
[Molecular Weight]

211.13
[MOL File]

618-88-2.mol
Chemical PropertiesBack Directory
[Appearance]

LIGHT CREAM CRYSTALLINE POWDER
[Melting point ]

259-261 °C(lit.)
[Boiling point ]

350.79°C (rough estimate)
[density ]

1.6342 (rough estimate)
[vapor pressure ]

0Pa at 25℃
[refractive index ]

1.5282 (estimate)
[Fp ]

120°C
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

Acetonitrile (Slightly, Heated), DMSO (Slightly), Methanol (Slightly)
[form ]

Solid
[pka]

2.81±0.10(Predicted)
[color ]

White to Off-White
[Water Solubility ]

Soluble in water.1.5 g/L at 20°C
[BRN ]

1976587
[InChI]

1S/C8H5NO6/c10-7(11)4-1-5(8(12)13)3-6(2-4)9(14)15/h1-3H,(H,10,11)(H,12,13)
[InChIKey]

NBDAHKQJXVLAID-UHFFFAOYSA-N
[SMILES]

OC(=O)c1cc(cc(c1)[N+]([O-])=O)C(O)=O
[LogP]

1.1 at 25℃
[CAS DataBase Reference]

618-88-2(CAS DataBase Reference)
[EPA Substance Registry System]

618-88-2(EPA Substance)
Questions And AnswerBack Directory
[Uses]

5-Nitrobenzene-1,3-Dicarboxylic Acid is used in the synthesis of Glycopyrrolate, a novel pharmaceutical compound based on PDE IV inhibitors; used in the treatment of respiratory complaints. Also used in the synthesis of coordination polymers.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313
[Hazard Codes ]

Xi,Xn
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
R40:Limited evidence of a carcinogenic effect.
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
S22:Do not breathe dust .
[RIDADR ]

2811
[WGK Germany ]

3
[TSCA ]

Yes
[REACH Registrations]

Active
[HS Code ]

29173990
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Nitric acid-->Isophthalic acid-->Nitroxylol-->3-Methyl-5-nitrobenzoic acid-->4-NITROISOPHTHALIC ACID
[Preparation Products]

5-AMINO-N-METHYLISOPHTHALAMIC ACID-->Dimethyl 5-nitroisophthalate-->5-Amino-2,4,6-triiodoisophthaloyl dichloride-->Dimethyl 5-aminoisophthalate-->5-Amino-2,4,6-triiodoisophthalic acid-->Iopamidol-->3,5-Bis(trifluoromethyl)nitrobenzene-->Methyl 5-nitroisophthalate-->DIETHYL 5-AMINOISOPHTHALATE HYDROCHLORIDE
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

5-Nitroisophthalic acid(618-88-2).msds
Hazard InformationBack Directory
[Chemical Properties]

LIGHT CREAM CRYSTALLINE POWDER
[Flammability and Explosibility]

Nonflammable
[Synthesis]

Isophthalic acid

121-91-5

5-Nitroisophthalic acid

618-88-2

The general procedure for the synthesis of 5-nitroisophthalic acid from isophthalic acid is as follows: concentrated sulfuric acid (120 mL, 2.21 mol) was added to a three-neck flask, followed by isophthalic acid (80 g, 0.48 mol). The mixture was heated to 75 °C and maintained at this temperature for 0.5 h under stirring conditions. 60% nitric acid (73.5 g, 0.70 mol) was slowly added dropwise, with the rate of acceleration of the drop being controlled to ensure completion of the drop within 2 to 2.5 hours. After the dropwise addition was completed, the reaction mixture was continued to be stirred at 75 °C for 2 hours. Subsequently, the temperature was raised to 90 °C and the reaction continued for 1 hour. Upon completion of the reaction, the mixture was cooled to below 50 °C and 120 mL of water was slowly added dropwise. The mixture was further cooled to room temperature, filtered, and the spent acid was removed by filtration. The filter cake was washed three times with pure water to remove the wash water. Pure water (120 mL) was added to the filter cake, stirred and heated until dissolved, stirring the mixture thoroughly. Hot filtration was carried out, cooled and crystallized, and the filter cake was dried to give a white crystalline solid 5-nitroisophthalic acid (89.6 g) in 88.3% yield.

[References]

[1] Patent: CN107721859, 2018, A. Location in patent: Paragraph 0025; 0027; 0029; 0031; 0033; 0034; 0035; 0036
[2] RSC Advances, 2016, vol. 6, # 10, p. 8495 - 8502
[3] Journal fuer Praktische Chemie (Leipzig), 1986, vol. 328, # 4, p. 497 - 514
[4] Langmuir, 2016, vol. 32, # 36, p. 9301 - 9312
[5] Acta Crystallographica Section C: Crystal Structure Communications, 1999, vol. 55, # 11, p. 1845 - 1847
Spectrum DetailBack Directory
[Spectrum Detail]

5-Nitroisophthalic acid(618-88-2)MS
5-Nitroisophthalic acid(618-88-2)1HNMR
5-Nitroisophthalic acid(618-88-2)13CNMR
5-Nitroisophthalic acid(618-88-2)IR1
5-Nitroisophthalic acid(618-88-2)IR2
5-Nitroisophthalic acid(618-88-2)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

5-Nitroisophthalic acid, 98%(618-88-2)
[Alfa Aesar]

5-Nitroisophthalic acid, 98%(618-88-2)
[Sigma Aldrich]

618-88-2(sigmaaldrich)
[TCI AMERICA]

5-Nitroisophthalic Acid,>99.0%(LC)(T)(618-88-2)
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