Technical Data

233434
CAS Number
100-01-6
Grade
GC
MDL Number
MFCD00007858
Molecular Formula
C₆H₆N₂O₂
Molecular Weight
138.13
EU Commodity Code
38220090
Shipping Temp
RT
Storage Temp
4°C
4-Nitroaniline 99+% (GC)
p-Nitroaniline; 1-Amino-4-nitrobenzene; 4-Amino-1-nitrobenzene; 4-Aminonitrobenzene; 4-Nitro-1-aminobenzene; 4-Nitrobenzenamine; 4-Nitrophenylamine; Azoamine Red Zh; C.I. 37035; C.I. Azoic Diazo Component 37; C.I. Developer 17; Developer P; Devol Red GG; Fast Red 2G Base; Fast Red Base 2J; Fast Red Base GG; Fast Red GG Base; Fast Red MP Base; Fast Red P Base; NSC 9797; Naphtoelan Red GG Base; Nitrazol CF extra; PNA; Red 2G Base; Shinnippon Fast Red GG Base; p-Aminonitrobenzene; p-Nitraniline; p-Nitrophenylamine; Albendazole Impurity 9

4-Nitroaniline is used in the synthesis of photorefractive polymers, as novel chromophores in analytical study. As well, due to the absorption spectrum associated with 4-Nitroaniline, it is used to determine catechol derivatives in syntheses.

Synonyms
p-Nitroaniline; 1-Amino-4-nitrobenzene; 4-Amino-1-nitrobenzene; 4-Aminonitrobenzene; 4-Nitro-1-aminobenzene; 4-Nitrobenzenamine; 4-Nitrophenylamine; Azoamine Red Zh; C.I. 37035; C.I. Azoic Diazo Component 37; C.I. Developer 17; Developer P; Devol Red GG; Fast Red 2G Base; Fast Red Base 2J; Fast Red Base GG; Fast Red GG Base; Fast Red MP Base; Fast Red P Base; NSC 9797; Naphtoelan Red GG Base; Nitrazol CF extra; PNA; Red 2G Base; Shinnippon Fast Red GG Base; p-Aminonitrobenzene; p-Nitraniline; p-Nitrophenylamine; Albendazole Impurity 9
CAS No
100-01-6
Molecular Formula
C₆H₆N₂O₂
Molecular Weight
138.13
Appearance
Light brown to dark brown crystalline powder
Purity (GC)
≥99%
NMR
Conforms to structur
Melting Point
147-150°C
Solubility
Ether, Benzene, Acetone, Alcohol, Chloroform
Storage and Stability
Store at 4°C under inert atmosphere. For maximum recovery of product, centrifuge the original vial prior to removing the cap.

Intended for research use only. Not for use in human, therapeutic, or diagnostic applications.

References
Convenient and Efficient Method for the Iodination of Aromatic Amines by Pyridinium Iodochloride|S. V. Khansole, S. B. Junne, M. A. Sayyed, Y. B. Vibhute, Synth. Commun. 2008, 38, 1792.
USBio References
No references available
United States Biological | 4 Technology Way | Salem, MA 01970
Phone 800-520-3011 | Fax 978-594-8052 | Website www.usbio.net