2-Ethylhexyl bromide
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2-Ethylhexyl bromide
structure -
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CAS No:
18908-66-2
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Formula:
C8H17Br
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Chemical Name:
2-Ethylhexyl bromide
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Synonyms:
1-BROMO ISO OCTANE;1-BROMO-2-ETHYLHEXANE;3-(bromomethyl)-heptan;Hexane, 1-bromo-2-ethyl;OCTYL BROMIDE;ISO-OCTYL BROMIDE;DL-1-BROMO-2-ETHYLHEXANE;BROMO ISOOCTANE
- Categories:
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CAS No:
2-Ethylhexyl bromide Basic Attributes
193.12
193.12
1098313
242-659-9
TSCA listed
Clear colorless to yellow
29033036
Characteristics
0
4.68
Clear colorless to yellow Liquid
1.086 g/mL at 25 °C(lit.)
-55°C (estimate)
75-77 °C16 mm Hg(lit.)
157 °F
n20/D1.4538(lit.)
insoluble
0-6°C
0.739mmHg at 25°C
2-8°C
Safety Information
3
Xi
26-36/37/39-37/39
Xi
Stable at room temperature in closed containers under normal storage and handling conditions.
P261-P305 + P351 + P338
36/37/38
|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 85 companies from 9 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
2-Ethylhexyl bromide Use and Manufacturing
Derived from the bromination of isooctyl alcohol. First mix isooctyl alcohol and red phosphorus, then slowly add liquid bromine, reflux for 4h after the addition is complete, the reaction is complete, add water to wash away the acid, dry, vacuum distillation to obtain the crude product, and then wash with concentrated sulfuric acid and water until neutral , Dried by calcium chloride and filtered to become the finished product.
Organic commonly used reagents. Used for dissolving insoluble polycyclic aromatic hydrocarbons. This compound can be added to the benzene ring to increase its solubility.
Introduction of the 2-ethylhexyl group in organic synthesis; preparation of disinfectants, pharmaceuticals.
2-Ethylhexyl bromide has been used in the synthesis of:methoxy-4-(2-ethylhexyloxy)benzenephotovoltaic conjugated polymer, having benzo[1,2-b:4,5-b′]difuran building block1-bromo-4-(2′-ethylhexyloxy)benzene3
Heptane, 3-(bromomethyl)-: ACTIVE
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