3-Bromo-1-propanol, 95%
3-Bromo-1-propanol, 95%
3-Bromo-1-propanol, 95%
Thermo Scientific Chemicals

3-Bromo-1-propanol, 95%

CAS: 627-18-9 | C3H7BrO | 138.99 g/mol
数量:
5 g
25 g
100 g
製品番号(カタログ番号) B22857.14
または、製品番号B22857-14
価格(JPY)
-
数量:
25 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS627-18-9
IUPAC Name3-bromopropan-1-ol
Molecular FormulaC3H7BrO
InChI KeyRQFUZUMFPRMVDX-UHFFFAOYSA-N
SMILESOCCCBr
さらに表示
FormLiquid
Appearance (Color)Clear colorless to pale yellow
Assay (GC)≥94.0
Identification (FTIR)Conforms
Refractive Index1.4865-1.4925 @ 20°C
3-Bromo-1-propanol is used in the synthesis of fluorescent halide-sensitive quinolinium dyes, chiral, quaternary prolines through cyclization of quaternary amino acids and molten salt-polymers. It is utilized for the study of micellar media and in microemulsions based on cationic or a nonionic surfactant by reacting with phenols. It acts as a grafting agent in the synthesis of recyclable reagents and an intermediate in the synthesis of organic molecules.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
3-Bromo-1-propanol is used in the synthesis of fluorescent halide-sensitive quinolinium dyes, chiral, quaternary prolines through cyclization of quaternary amino acids and molten salt-polymers. It is utilized for the study of micellar media and in microemulsions based on cationic or a nonionic surfactant by reacting with phenols. It acts as a grafting agent in the synthesis of recyclable reagents and an intermediate in the synthesis of organic molecules.

Solubility
Miscible with water. Slightly miscible with ethanol and ether.

Notes
Store in cool place. Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Vaidyanathan, G.; McDougald, D.; Koumarianou, E.; Choi, J.; Hens, M.; Zalutsky, M. R. Synthesis and evaluation of 4-[18F]fluoropropoxy-3-iodobenzylguanidine ([18F]FPOIBG): A novel 18F-labeled analogue of MIBG. Nucl. Med. Biol. 2015, 42 (8), 673-684.
  2. Nozoe, A.; Morisada, S.; Ohto, K.; Kawakita, H. Preparation of 1,2,3-Triazole-Containing Resins for Adsorption of Palladium Ions. Solvent Extr. Ion Exch. 2015, 33 (1), 56-64.