1-Bromopropane (CAS 106-94-5)
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1-Bromopropane, a halogenated hydrocarbon, is primarily utilized in organic synthesis and as a solvent in various research applications. Its molecular structure, characterized by a three-carbon chain with a bromine atom attached to the terminal carbon, makes it particularly effective in nucleophilic substitution reactions, a foundational mechanism in organic chemistry. This reaction type allows for the replacement of the bromine atom with other functional groups, thereby enabling the synthesis of a wide range of organic compounds. The ability of 1-bromopropane to participate in such reactions makes it useful in the development of new materials, pharmaceuticals, and complex molecules for research purposes. Its utility extends to laboratories focused on understanding chemical interactions and properties, where it is employed in experimental protocols to elucidate mechanisms of reaction and to explore the synthesis of novel compounds with potential applications in various fields of chemistry.
1-Bromopropane (CAS 106-94-5) References
- Large-scale label-free proteomics analysis of occupational poisoned patients of 1-bromopropane, workers exposed to 1-bromopropane and healthy individuals. | Miao, R., et al. 2018. Hum Exp Toxicol. 37: 3-12. PMID: 28120620
- [A meta-analysis of the effect of occupational exposure to 1-bromopropane on workers' nerve conduction velocity]. | Lin, ZX., et al. 2018. Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 36: 343-346. PMID: 29996378
- NMDA Receptor Antagonist MK801 Protects Against 1-Bromopropane-Induced Cognitive Dysfunction. | Xu, L., et al. 2019. Neurosci Bull. 35: 347-361. PMID: 30569431
- [Changes in mass spectrometry of proteins in patients with 1-bromopropane poisoning after treatment]. | Miao, RM., et al. 2019. Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 37: 34-37. PMID: 30884586
- Identification of DNA and glutathione adducts in male Sprague-Dawley rats exposed to 1-bromopropane. | Nepal, MR., et al. 2019. J Toxicol Environ Health A. 82: 502-513. PMID: 31140386
- Exposure to 1-bromopropane vapors during pregnancy enhances the development of hippocampal neuronal excitability in rat pups during lactation. | Fueta, Y., et al. 2020. J Occup Health. 62: e12135. PMID: 32715571
- Corrigendum to '28-day somatic gene mutation study of 1-Bromopropane in female big blue® B6C3F1 Mice via whole-Body inhalation: Support for a carcinogenic threshold' [Regul. Toxicol. Pharmacol., 104 (2019) 1-7]. | Stelljes, M., et al. 2020. Regul Toxicol Pharmacol. 118: 104814. PMID: 33158580
- Binding-Induced Unfolding of 1-Bromopropane in α-Cyclodextrin. | Urbina, AS., et al. 2020. J Phys Chem B. 124: 11015-11021. PMID: 33205979
- 1-Bromopropane-induced apoptosis in OVCAR-3 cells via oxidative stress and inactivation of Nrf2. | Yang, G., et al. 2021. Toxicol Ind Health. 37: 59-67. PMID: 33305700
- Cerebral excitability in pup rats prenatally exposed to 1-bromopropane is suppressed by bromide accumulated in the brain. | Fueta, Y., et al. 2021. Ind Health. 59: 239-248. PMID: 34261823
- Biomarkers of exposure and effect in the serum and urine of rats or workers exposed to 1-bromopropane. | Zhang, Y., et al. 2022. Toxicol Ind Health. 38: 351-364. PMID: 35532359
- Cross-sectional and longitudinal relationships between urinary 1-bromopropane metabolite and pulmonary function and underlying role of oxidative damage among urban adults in the Wuhan-Zhuhai cohort in China. | Wang, B., et al. 2022. Environ Pollut. 313: 120147. PMID: 36096263
- [A case of ataxic gait disturbance due to 1-bromopropane neurotoxicity]. | Morishima, Y., et al. 2023. Rinsho Shinkeigaku. 63: 27-30. PMID: 36567103
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
1-Bromopropane, 5 ml | sc-255818 | 5 ml | $29.00 | |||
1-Bromopropane, 100 ml | sc-255818A | 100 ml | $22.00 |