ChemicalBook > Product Catalog >Organic Chemistry >Amides >Naphthenic amines derivatives >4-Bromoaniline

4-Bromoaniline

4-Bromoaniline Structure
CAS No.
106-40-1
Chemical Name:
4-Bromoaniline
Synonyms
P-BROMOANILINE;bromoaniline;4-Bromoanilines;4-BROMOBENZENAMINE;4-bromo-benzenamin;p-BROMOANILINE pure;4-BroMo-phenylaMine;4-BromoaniL;4-Bromanilinu;4-bromoanline
CBNumber:
CB9760655
Molecular Formula:
C6H6BrN
Molecular Weight:
172.02
MOL File:
106-40-1.mol
MSDS File:
SDS
Modify Date:
2024/7/29 18:03:56

4-Bromoaniline Properties

Melting point 56-62 °C (lit.)
Boiling point 230-250 °C
Density 1.497
refractive index 1.5680 (estimate)
Flash point 222-224°C
storage temp. Store below +30°C.
solubility ethanol: soluble0.5g/10 mL, clear, colorless to almost colorless
pka 3.86(at 25℃)
form crystalline
color white to light yellow
Odor Sweetish
Water Solubility <0.1 g/100 mL at 23 ºC
Merck 14,1404
BRN 742031
Dielectric constant 13.0(-7℃)
Stability Stable. Combustible. Incompatible with strong oxidizing agents, peroxides, acids, acid chlorides, acid anhydrides, chloroformates. May be air sensitive.
InChIKey WDFQBORIUYODSI-UHFFFAOYSA-N
CAS DataBase Reference 106-40-1(CAS DataBase Reference)
NIST Chemistry Reference 4-Bromoaniline(106-40-1)
EPA Substance Registry System p-Bromoaniline (106-40-1)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS06,GHS08,GHS09
Signal word  Danger
Hazard statements  H302-H311+H331-H373-H410
Precautionary statements  P273-P280-P301+P312-P302+P352+P312-P304+P340+P311-P314
Hazard Codes  Xn
Risk Statements  21/22-36/37/38-20/21/22
Safety Statements  26-36/37-36/37/39
RIDADR  UN 2811 6.1/PG 3
WGK Germany  3
RTECS  BW9280000
8-9-23
Hazard Note  Harmful
TSCA  Yes
HazardClass  6.1
PackingGroup  III
HS Code  29214210
Toxicity LD50 orally in Rabbit: 456 mg/kg LD50 dermal Rat 536 mg/kg
NFPA 704
1
3 1

4-Bromoaniline price More Price(22)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 16230 4-Bromoaniline ≥99.0% (GC) 106-40-1 25G ₹7664.1 2022-06-14 Buy
Sigma-Aldrich(India) 8.01600 4-Bromoaniline for synthesis 106-40-1 100G ₹13980 2022-06-14 Buy
Sigma-Aldrich 100900 4-Bromoaniline 97% 106-40-1 5G ₹1948.5 2022-06-14 Buy
Sigma-Aldrich(India) 100900 4-Bromoaniline 97% 106-40-1 5G ₹1948.5 2022-06-14 Buy
Sigma-Aldrich(India) 16230 4-Bromoaniline ≥99.0% (GC) 106-40-1 100G ₹24681 2022-06-14 Buy
Product number Packaging Price Buy
16230 25G ₹7664.1 Buy
8.01600 100G ₹13980 Buy
100900 5G ₹1948.5 Buy
100900 5G ₹1948.5 Buy
16230 100G ₹24681 Buy

4-Bromoaniline Chemical Properties,Uses,Production

Chemical Properties

Gray-brown crystals with a peculiar odor. When heated or burned, they break down and release harmful fumes that contain hydrogen bromide and nitrogen oxides. When dissolved in water, it acts as a mild base. It reacts with acids and powerful oxidizing agents. The compound 4-bromoaniline consists of a hydrophobic benzene ring and an amino group that assists in carrying substances and improving PSC stability.

Uses

4-Bromoaniline is a brominated aniline that is commonly used as a building block in the preparation of pharmaceutical and organic compounds. It is used in the preparation of azo dyes and is condensed with formaldehyde to prepare dihydroquinazolines. In addition, 4-Bromoaniline is also used as an intermediate in the production of other chemicals such as metobromuron, a herbicide, and resorantel, an antiparasitic agent.

Preparation

4-bromoaniline can be made by reacting aniline with bromine with a protection with acetyl chloride.

General Description

P-bromoaniline is a brown solid with a sweet odor. (NTP, 1992)

Air & Water Reactions

4-Bromoaniline is sensitive to prolonged exposure to air. Vapor may form highly reactive mixtures in air . Insoluble in water.

Reactivity Profile

Vapor may form highly reactive mixtures in air.

Fire Hazard

Flash point data are not available for 4-Bromoaniline, but 4-Bromoaniline is probably combustible.

Synthesis

RGO/Cu NPs (25 mg), arylboronic acid (1.0 mmol), K2CO3(1.3 mmol), 25-28% aqueous ammonia (5 mmol) and methanol(4 mL) were added to a 50 mL round-bottomed flask. The reactionmixture was stirred under reflux conditions for the appropriatetime. After completion of the reaction as monitored by TLC, themixture was filtered, and the solvent of the filtrate was removedunder vacuum with the aid of a rotary evaporator. The residue waspurified by column chromatography on silica gel to afford 4-Bromoaniline.

Purification Methods

Crystallise the aniline (with appreciable loss) from aqueous EtOH. The benzoyl derivative has m 204o (from EtOH). [Beilstein 12 IV 1497.]

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