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8-Bromooctanoic acid
[CAS# 17696-11-6]

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Complete supplier list of 8-Bromooctanoic acid
Identification
Classification Chemical reagent >> Organic reagent >> Fatty acid
Name 8-Bromooctanoic acid
Synonyms 8-Bromocaprylic acid
Molecular Structure CAS # 17696-11-6, 8-Bromooctanoic acid, 8-Bromocaprylic acid
Molecular Formula C8H15BrO2
Molecular Weight 223.11
CAS Registry Number 17696-11-6
EC Number 605-788-5
SMILES C(CCCC(=O)O)CCCBr
Properties
Density 1.3±0.1 g/cm3, Calc.*
Melting point 35-37 ºC (Expl.)
Index of Refraction 1.487, Calc.*
Boiling Point 316.0±0.0 ºC (760 mmHg), Calc.*, 147-150 ºC (2 mmHg) (Expl.)
Flash Point 136.8±23.2 ºC, Calc.*
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbols symbol   GHS05 Danger    Details
Hazard Statements H314    Details
Precautionary Statements P260-P264-P280-P301+P330+P331-P302+P361+P354-P304+P340-P305+P354+P338-P316-P321-P363-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Skin corrosionSkin Corr.1BH314
Serious eye damageEye Dam.1H318
Specific target organ toxicity - single exposureSTOT SE3H335
Substances or mixtures corrosive to metalsMet. Corr.1H290
Skin corrosionSkin Corr.1CH314
Transport Information UN 3261
SDS Available
up Discovory and Applicatios
8-Bromooctanoic acid is a brominated fatty acid compound that contains a bromine atom at the eighth position of the octanoic acid chain. It is a derivative of octanoic acid, an eight-carbon fatty acid, where the hydrogen at the eighth carbon is replaced by a bromine atom. This structural modification imparts distinct chemical reactivity and makes 8-bromooctanoic acid an interesting compound for use in organic synthesis and various industrial applications. Its ability to undergo nucleophilic substitution reactions and its influence on the physicochemical properties of other molecules have made it a useful intermediate in multiple chemical processes.

The discovery of 8-bromooctanoic acid arose from the growing interest in functionalized fatty acids and their derivatives. Brominated fatty acids have been studied for their unique reactivity, as the bromine atom can easily participate in chemical reactions, such as substitution or elimination reactions. These reactions are often exploited in the synthesis of more complex molecules, as the bromine atom can be replaced by other functional groups, allowing for the development of a wide range of compounds. The presence of the bromine atom also alters the compound's solubility and biological properties, which has been explored in several applications.

One of the major applications of 8-bromooctanoic acid is in the pharmaceutical industry. The compound can serve as an intermediate in the synthesis of bioactive molecules, particularly those with antimicrobial or anti-inflammatory properties. The bromine atom can enhance the molecule’s interaction with biological targets, such as enzymes or receptors, making it more effective in its intended therapeutic roles. Additionally, the incorporation of a bromine atom can improve the metabolic stability of the compound, making it more resistant to degradation by enzymes. As a result, 8-bromooctanoic acid and its derivatives have been investigated for potential use in drug development, especially for conditions where traditional treatments may not be as effective.

In addition to its pharmaceutical applications, 8-bromooctanoic acid has potential uses in material science, particularly in the synthesis of polymers and advanced materials. The presence of the bromine atom provides a unique site for chemical modification, which can be exploited to create new materials with tailored properties. For example, 8-bromooctanoic acid can be incorporated into polymerization reactions to create polymer chains with specific characteristics, such as enhanced conductivity or solubility. This versatility makes it a valuable building block for the development of new materials for use in industries such as electronics, coatings, and adhesives.

8-bromooctanoic acid is also of interest in the field of environmental chemistry. Brominated compounds, including fatty acids, have been studied for their potential applications in water treatment and waste management. The ability of brominated fatty acids to interact with certain pollutants, such as heavy metals or organic contaminants, has been explored as a method for removing these substances from water or soil. Research continues to investigate the role of such compounds in environmental remediation and pollution control.

In conclusion, 8-bromooctanoic acid is a versatile and valuable compound with a wide range of applications in pharmaceutical, material science, and environmental chemistry. Its unique reactivity, conferred by the bromine atom, allows it to be used as an intermediate in drug synthesis, the production of advanced materials, and even environmental applications. Ongoing research into its properties and applications continues to expand its potential uses across various industries.
Market Analysis Reports
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