化驗
97%
形狀
solid
mp
38-40 °C (lit.)
溶解度
95% ethanol: soluble 50 mg/mL, clear, colorless to faintly yellow
SMILES 字串
OC(=O)CCCCBr
InChI
1S/C5H9BrO2/c6-4-2-1-3-5(7)8/h1-4H2,(H,7,8)
InChI 密鑰
WNXNUPJZWYOKMW-UHFFFAOYSA-N
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應用
5-溴戊酸被用于制备：
- 通过与1,1-二甲基-1,3-丙二胺的反应生成5-（3-二甲基氨）丙基戊酸戊酸酯溴化物
- 被羧酸基团官能化的纳米金刚石
- 水溶性钾石墨纳米片
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
230.0 °F - closed cup
閃點（°C）
110 °C - closed cup
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
其他客户在看
Oleksandr Kuznetsov et al.
Langmuir : the ACS journal of surfaces and colloids, 28(11), 5243-5248 (2012-03-01)
Reduction of the graphenic edges of annealed nanodiamond by sodium in liquid ammonia leads to a nanodiamond salt that reacts with either alkyl or aryl halides by electron transfer to yield radical anions that dissociate spontaneously into free radicals and
Functionalization of potassium graphite.
Soma Chakraborty et al.
Angewandte Chemie (International ed. in English), 46(24), 4486-4488 (2007-05-05)
Natashya Falcone et al.
Chembiochem : a European journal of chemical biology, 20(6), 838-845 (2018-12-01)
Nicotinamide and pyridine-containing conjugates have attracted a lot of attention in research as they have found use in a wide range of applications including as redox flow batteries and calcium channel blockers, in biocatalysis, and in metabolism. The interesting redox
Caixia Yue et al.
Theranostics, 6(13), 2352-2366 (2016-11-24)
Mitochondria in cancer cells maintain a more negative membrane potential than normal cells. Mitochondria are the primary source of cellular reactive oxygen species (ROS), which are necessary for photodynamic therapy. Thus, the strategy of targeting mitochondria can maximize the photodynamic
Iwona Kowałczyk
Acta chimica Slovenica, 61(1), 39-50 (2014-03-26)
3-(3-Dimethylammonio)propylammonio propanoate bromide (1), 4-(3-dimethylammonio)propylammonio butanoate bromide (2), and 5-(3-dimethylammonio)propylammonio pentanoate bromide (3) have been obtained in reaction of 1,1-dimethyl-1,3-propylenediamine with 3-bromopropionic acid, ethyl 4-bromobutyrate and 5-bromovaleric acid, respectively. The products have been characterized by FTIR, Raman and NMR spectroscopy.
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