| Identification | More | [Name]
p-Bromophenoxyacetic acid | [CAS]
1878-91-7 | [Synonyms]
4'-BROMOPHENOXYACETIC ACID
4-BROMOPHENOXYACETIC ACID
AKOS BBB/216
AKOS BBS-00001063
IFLAB-BB F1924-0026
LABOTEST-BB LT00000328
P-BROMOPHENOXYACETIC ACID
Acetic acid, 2-(4-bromophenoxy)- | [EINECS(EC#)]
217-530-5 | [Molecular Formula]
C8H7BrO3 | [MDL Number]
MFCD00093070 | [Molecular Weight]
231.04 | [MOL File]
1878-91-7.mol |
| Chemical Properties | Back Directory | [Appearance]
White or cream crystalline powder | [Melting point ]
149-153 °C(lit.)
| [Boiling point ]
337.9±17.0 °C(Predicted) | [density ]
1.6494 (rough estimate) | [refractive index ]
1.4730 (estimate) | [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
soluble in Methanol | [form ]
powder to crystal | [pka]
3.09±0.10(Predicted) | [color ]
White to Almost white | [CAS DataBase Reference]
1878-91-7(CAS DataBase Reference) | [EPA Substance Registry System]
1878-91-7(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Safety Statements ]
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [TSCA ]
Yes | [HazardClass ]
IRRITANT | [HS Code ]
29189900 |
| Hazard Information | Back Directory | [Chemical Properties]
White or cream crystalline powder | [Uses]
4-Bromophenoxyacetic acid may be used as a starting material in the preparation of radioiodinated phenoxyacetic acid derivatives with potential application as radiopharmaceuticals. | [General Description]
4-Bromophenoxyacetic acid, also known as p-bromophenoxyacetate, is a phenoxyalkanoic acid derivative. It is a chemical elicitor that can induce β-glucuronidase (GUS) activity in rice. | [Synthesis]
The general procedure for the synthesis of 4-bromophenoxyacetic acid from 4-bromophenol and chloroacetic acid was as follows: a mixture of NaOH (0.04 mol, 1.60 g), deionized water (20 mL), and ethanol (20 mL) was added to a 150 mL three-necked flask, followed by the slow addition of 4-bromophenol (0.04 mol, 6.92 g). After 20 minutes of reaction under stirring, aqueous sodium chloroacetate solution was added dropwise. The reaction mixture was heated to 105 °C and refluxed for 5 hours. After completion of the reaction, it was cooled to room temperature and the pH of the mixture was adjusted to 1-2 with dilute hydrochloric acid. the precipitate was collected by filtration and washed several times with dilute hydrochloric acid. Finally, the product was purified by recrystallization and dried under vacuum to give 4-bromophenoxyacetic acid as a white solid. | [Purification Methods]
Crystallise the acid from EtOH or H2O (m 161.4-161.8o). [Hayes & Branch J Am Chem Soc 65 1555 1943, Beilstein 6 III 747, 6 IV 1052.] | [References]
[1] Luminescence, 2018, vol. 33, # 5, p. 855 - 862
[2] Synthetic Communications, 2004, vol. 34, # 3, p. 377 - 382
[3] Journal of Molecular Structure, 2014, vol. 1074, p. 487 - 495
[4] Journal of Fluorescence, 2015, vol. 25, # 4, p. 849 - 859
[5] Luminescence, 2015, vol. 30, # 5, p. 677 - 685 |
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