ChemicalBook > CAS DataBase List > 4-Nitrophthalimide

4-Nitrophthalimide

Product Name
4-Nitrophthalimide
CAS No.
89-40-7
Chemical Name
4-Nitrophthalimide
Synonyms
5-NITROISOINDOLINE-1,3-DIONE;5-NITROPHTHALIMIDE;AKOS B028733;4-Nitrophtalimide;4-NITROPHTHALIMIDE;4-nitro-phthalimid;4-Nirtophthalimide;P-NITRO-PHTHALIMIDE;PHTHALIMIDE, 4-NITRO-;4-Nitrophthalimide>
CBNumber
CB3681521
Molecular Formula
C8H4N2O4
Formula Weight
192.13
MOL File
89-40-7.mol
More
Less

4-Nitrophthalimide Property

Melting point:
206 °C
Boiling point:
328.09°C (rough estimate)
Density 
1.5513 (rough estimate)
refractive index 
1.4900 (estimate)
storage temp. 
Sealed in dry,Room Temperature
form 
powder to crystal
pka
7.79±0.20(Predicted)
color 
Yellow powder
Water Solubility 
<0.01 g/100 mL at 18 ºC
BRN 
180224
Stability:
Stable. Combustible. Incompatible with moisture, water, strong oxidising agents, strong bases.
InChIKey
ANYWGXDASKQYAD-UHFFFAOYSA-N
CAS DataBase Reference
89-40-7(CAS DataBase Reference)
NIST Chemistry Reference
4-Nitro-phthalimide(89-40-7)
EPA Substance Registry System
4-Nitrophthalimide (89-40-7)
More
Less

Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
37/39-26-36-24/25
WGK Germany 
3
RTECS 
TI5625000
Hazard Note 
Irritant
TSCA 
Yes
HS Code 
29251900
Toxicity
mmo-sat 333 mg/plate EMMUEG 11(Suppl 12),1,88
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
332097
Product name
4-Nitrophthalimide
Purity
98%
Packaging
5g
Price
$77.7
Updated
2024/03/01
Sigma-Aldrich
Product number
332097
Product name
4-Nitrophthalimide
Purity
98%
Packaging
25g
Price
$327
Updated
2024/03/01
TCI Chemical
Product number
N0247
Product name
4-Nitrophthalimide
Purity
>98.0%(HPLC)(T)
Packaging
25g
Price
$31
Updated
2024/03/01
TCI Chemical
Product number
N0247
Product name
4-Nitrophthalimide
Purity
>98.0%(HPLC)(T)
Packaging
500g
Price
$300
Updated
2024/03/01
Alfa Aesar
Product number
A12040
Product name
4-Nitrophthalimide, 98%
Packaging
5g
Price
$38.85
Updated
2023/01/06
More
Less

4-Nitrophthalimide Chemical Properties,Usage,Production

Chemical Properties

slight yellow powder

Uses

4-Nitrophthalimide is used as intermediate of organic synthesis and fluorescent dyes, it can be used to produce azo dyes, luminol, etc. It can also be used to prepare 4-nitrophthalonitrile, 5-cyanophthalide and other drug intermediates.

Preparation

4-Nitrophthalimide is synthesized from phthalimide by nitration. Cool the fuming nitric acid to below 5°C, slowly add concentrated sulfuric acid dropwise, and control the temperature to 10-13°C. Plus phthalimide. Leave at room temperature overnight. Then, it was poured into ice water with stirring, and the precipitate was precipitated below 20°C. Filter, wash with water, dry, and then recrystallize from ethanol to obtain 4-nitrophthalimide with a yield of 60%.

General Description

Yellow powder.

Air & Water Reactions

4-Nitrophthalimide can be hydrolyzed. . Insoluble in water.

Reactivity Profile

A nitrated amine. Amines are combustible. The combustion of amines yields noxious NOx. REACTIVITY - Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides. Aromatic nitro compounds range from slight to strong oxidizing agents. If mixed with reducing agents, including hydrides, sulfides and nitrides, they may begin a vigorous reaction that culminates in a detonation. The aromatic nitro compounds may explode in the presence of a base such as sodium hydroxide or potassium hydroxide even in the presence of water or organic solvents. The explosive tendencies of aromatic nitro compounds are increased by the presence of multiple nitro groups.

Fire Hazard

Flash point data for 4-Nitrophthalimide are not available, however 4-Nitrophthalimide is probably combustible.

Safety Profile

Mutation data reported. Whenheated to decomposition it emits toxic vapors of NOx.

Synthesis

200 mL of sulfuric acid and 50 mL of fuming nitric acid were cooled on an ice bath and 40 g (0.272 mol) phthalimide was added in portions within 1-1.5 hours so as not to exceed the internal temperature beyond 10-15 ??C. The mixture was stirred over ice bath for half an hour and the internal temperature was raised to 35 ??C, and yellow particles were observed to dissolve. The mixture was stirred for an additional 1 hour, then cooled to 0 ??C again and poured onto 1 kg of ice water mixture. Yellow 4-nitrophthalonitrile precipitated, it was filtered and washed with water until the filtrate was neutral to blue litmus paper. It was crystallized from 850-900 mL of ethyl alcohol. Bright yellow crystals were filtered, washed with cold ethyl alcohol, and dried in a vacuum oven at 80-90 ??C.

4-Nitrophthalimide Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

4-Nitrophthalimide Suppliers

Greenspring Biotechnology (Jiangsu) Co., Ltd.
Tel
0523-87726088 13705266400
Fax
0523-87653988
Email
sun1@sunmy.com
Country
China
ProdList
116
Advantage
58
SiChuang NanBu Honesty Technology Co., Ltd.
Tel
0838-5675166 15883665058
Fax
0838-5675535
Email
nbcxkj@126.com
Country
China
ProdList
667
Advantage
55
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
94657
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
021-61259108 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30123
Advantage
84
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24529
Advantage
81
Beijing dtftchem Technology Co., Ltd.
Tel
010-60275820 13031183356
Fax
010-60270825
Email
elainezt@sina.com
Country
China
ProdList
1390
Advantage
62
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44689
Advantage
61
JinYan Chemicals(ShangHai) Co.,Ltd.
Tel
13817811078
Fax
86-021-50426522,50426273
Email
sales@jingyan-chemical.com
Country
China
ProdList
9976
Advantage
60
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
Country
China
ProdList
42958
Advantage
64
More
Less

View Lastest Price from 4-Nitrophthalimide manufacturers

Asia Chem I and E (Jiangsu) Co Ltd
Product
4-Nitrophthalimide 89-40-7
Price
US $25.12/Kg/Drum
Min. Order
25Kg/Drum
Purity
99.00%HPLC
Supply Ability
10tons/month
Release date
2021-09-18
Hebei Chuanghai Biotechnology Co,.LTD
Product
4-Nitrophthalimide 89-40-7
Price
US $10.70/kg
Min. Order
10kg
Purity
99%
Supply Ability
10000kg
Release date
2024-08-23
Hebei Weibang Biotechnology Co., Ltd
Product
4-Nitrophthalimide 89-40-7
Price
US $1.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
10 mt
Release date
2021-08-16

89-40-7, 4-NitrophthalimideRelated Search:


  • AKOS B028733
  • 5-NITRO-1,3-DIHYDRO-2H-ISOINDOL-1,3-DIONE
  • 5-NITRO-1H-ISOINDOLE-1,3(2H)-DIONE
  • 4 - nitro phthalates forMyl aMine
  • 5-NITROPHTHALIMIDE
  • 5-NITROISOINDOLINE-1,3-DIONE
  • 5-NITROISOINDOLE-1,3-DIONE
  • 4-NITRO-1,2-BENZENE DICARBOXYLIC ACID, IMIDE
  • 4-NITROPHTHALIMIDE
  • PHTHALIMIDE, 4-NITRO-
  • P-NITRO-PHTHALIMIDE
  • 1H-Isoindole-1,3(2H)-dione, 5-nitro-
  • 4-nitro-phthalimid
  • 5-nitro-1h-isoindole-3(2h)-dione
  • 4-Nirtophthalimide
  • 5-Nitro-2H-isoindole-1,3-dione
  • 4-Nitrophthalimide,98%
  • 4-Nitrophtalimide
  • 4-Nitrophthalimide&gt
  • 4-Nitrophthalimide ISO 9001:2015 REACH
  • 4-NITRO PHTHALIMIDE/4-Nitrophthalimide
  • 89-40-7
  • C8H4N2O4
  • Organic Building Blocks
  • Cyclic Imides
  • Building Blocks
  • Carbonyl Compounds
  • Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
  • N
  • Stains and Dyes
  • Stains&Dyes, A to