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4-Bromophthalonitrile

CAS No.
70484-01-4
Chemical Name:
4-Bromophthalonitrile
Synonyms
4-Bromophthalonitrile;4-Bromo-1,2-dicyanobenzene;4-Bromo-1,2-benzenedicarbonitrile;4-bromobenzene-1,2-dicarbonitrile;1,2-Benzenedicarbonitrile, 4-broMo-;1,2-Benzenedicarbonitrile, 4-broMo- 4-BroMo-1,2-benzenedicarbonitrile
CBNumber:
CB8162663
Molecular Formula:
C8H3BrN2
Molecular Weight:
207.03
MDL Number:
MFCD00221794
MOL File:
70484-01-4.mol
MSDS File:
SDS
Last updated:2026-09-12 18:55:23

4-Bromophthalonitrile Properties

Melting point 138.0 to 142.0 °C
Boiling point 325.1±27.0 °C(Predicted)
Density 1.68±0.1 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility Chloroform (Slightly), Methanol (Slightly, Heated)
form Solid
color Pale Beige

SAFETY

Risk and Safety Statements

Symbol(GHS)  Skull and Crossbones (GHS06)
GHS06
Signal word  Danger
Hazard statements  H301+H311+H331-H315-H319
Precautionary statements  P501-P261-P270-P271-P264-P280-P337+P313-P305+P351+P338-P361+P364-P332+P313-P301+P310+P330-P302+P352+P312-P304+P340+P311-P403+P233-P405
RIDADR  3439
HazardClass  6.1
PackingGroup 
HS Code  2926907090
NFPA 704
0
3 0

4-Bromophthalonitrile price More Price(62)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical B5509 4-Bromophthalonitrile >97.0%(GC) 70484-01-4 1g $85 2026-04-30 Buy
TCI Chemical B5509 4-Bromophthalonitrile >97.0%(GC) 70484-01-4 5g $295 2026-04-30 Buy
TRC TRC-B688153-500MG 4-Bromophthalonitrile 70484-01-4 500mg $91 2026-06-03 Buy
TRC TRC-B688153-250MG 4-Bromophthalonitrile 70484-01-4 250mg $72 2026-06-03 Buy
TRC TRC-B688153-1G 4-Bromophthalonitrile 70484-01-4 1g $133 2026-06-03 Buy
Product number Packaging Price Buy
B5509 1g $85 Buy
B5509 5g $295 Buy
TRC-B688153-500MG 500mg $91 Buy
TRC-B688153-250MG 250mg $72 Buy
TRC-B688153-1G 1g $133 Buy

4-Bromophthalonitrile Chemical Properties, Uses, Production

Uses

4-Bromophthalonitrile is formed from the oxidative ammonolysis of 4-bromo-o-xylene.

Synthesis

1,2-BenzenedicarboxaMide, 4-broMo-

490038-15-8

4-BROMOPHTHALONITRILE

70484-01-4

The general procedure for the synthesis of 4-bromophthalonitrile (4-BPN) from 4-bromophthalamide (4-BPA) was as follows: in a 200 mL aubergine flask, 100 mL of dry N,N-dimethylformamide (DMF) was added, and 70 mL of thionyl chloride was added slowly dropwise under the conditions of an ice bath at 0°C, with the acceleration of dropwise acceleration being controlled to keep the temperature of the reaction from exceeding 5°C. After the dropwise acceleration, the mixture was allowed to stand for 2 hr at 0°C. The mixture was allowed to stand at 0°C for 2 hours. Subsequently, 20.9032 g (0.086 mol) of 4-BPA powder was slowly added and the reaction temperature continued to be controlled to not exceed 5°C. After maintaining the reaction temperature in the range of 0 to 5°C for 5 hrs, the ice bath was removed and the reaction system was warmed to 23°C and the reaction continued for 24 hrs. Upon completion of the reaction, the reaction solution (which appeared as a white to yellow suspension) was slowly poured into a 1 L beaker containing 300 g of ice. The precipitated white to yellow crystals were collected by filtration under reduced pressure and washed sequentially with 100 mL of purified water and 100 mL of methanol. The crude product was dissolved in 10 times its weight in methanol and heated using an oil bath until completely dissolved, then left to recrystallize at 23°C. The product was dried under reduced pressure. The resulting white crystals were dried under reduced pressure for 24 h to give 17.80 g (yield: 80%) of 4-BPN. The structure of the product was confirmed by 1H-NMR spectrum (CDCl3, ppm): 7.96 (dd, 1H), 7.90 (dd, 1H), 7.67 (d, 1H).

References

[1] Patent: EP2206749, 2010, A1. Location in patent: Page/Page column 23
[2] Patent: JP5906522, 2016, B2. Location in patent: Paragraph 0058; 0059
[3] Helvetica Chimica Acta, 2004, vol. 87, # 4, p. 825 - 844

4-Bromophthalonitrile Preparation Products And Raw materials

Raw materials

Preparation Products

Global Suppliers ( 114)
Supplier Tel Email Country ProdList Advantage
Meryer (Shanghai) Chemical Technology Co., Ltd. 4006356688 18621169109 market03@meryer.com China 40202 62
TCI (Shanghai) Development Co., Ltd. 021-67121386 Sales-CN@TCIchemicals.com China 24512 81
Energy Chemical 400-0056266 sales8178@energy-chemical.com China 44850 61
Shanghai Hanhong Scientific Co.,Ltd. 021-54306202 13764082696 info@hanhongsci.com China 42917 64
Shandong Xiya Chemical Co., Ltd 13355009207 13355009207 3007715519@qq.com China 18722 57
Shanghai Sunway Pharmaceutical Technology Co., Ltd 13761987713 hxzheng@sunwaypharm.cn China 8663 57
Hangzhou Sage Chemical Co., Ltd. +86057186818502 13588463833 info@sagechem.com China 10265 58
TOKYO CHEMICAL INDUSTRY CO., LTD. 03-36680489 Sales-JP@TCIchemicals.com Japan 28364 80
TCI Europe 320-37350700 sales@tcieurope.eu Europe 23654 75
TCI AMERICA 800-4238616 sales@tciamerica.com Americas 23636 75

View Latest Price from 4-Bromophthalonitrile manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
4-BROMOPHTHALONITRILE pictures 2020-01-09 4-BROMOPHTHALONITRILE
70484-01-4
$1.00 1KG 99% 200kg Career Henan Chemical Co

4-Bromophthalonitrile Spectrum

4-bromobenzene-1,2-dicarbonitrile 1,2-Benzenedicarbonitrile, 4-broMo- 1,2-Benzenedicarbonitrile, 4-broMo- 4-BroMo-1,2-benzenedicarbonitrile 4-Bromo-1,2-dicyanobenzene 4-Bromo-1,2-benzenedicarbonitrile 4-Bromophthalonitrile 70484-01-4 2739-85-2 C8H3BrN2