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1-Bromopentane / 5 G

Purity: 98 %
Synonym: n-Amyl bromide; Pentyl bromide; C5H11Br
Molecular Formula: CH3(CH2)4Br
Molecular Weight: 151.04
SKU: MND-49911
CAS Number: 110-53-2
MDL number: MFCD00000267
EC Number: 203-776-0
Note: Prices are for comparison only. Contact Sales for current pricing.
Packing size: 5 G  
20.23 EUR



Safety Information


Hazard Statements

H315
H411
H226

Precautionary Statements

P210
P273
P302 + P352

Pictograms



Properties

Signal WordWarning
Flash Point (C)30 °C
Flash Point (F)86.0 °F
Vapor Density>1 (vs air)
Density1.218 g/mL at 25 °C (lit.)
Boiling Point130 °C (lit.)
Melting Point−95 °C (lit.)

 Product Description

1-BROMOPENTANE is a halogenated organic compound commonly used as a solvent and intermediate in organic synthesis. It serves as a starting material for the production of various chemicals, including pharmaceuticals, agrochemicals, and specialty chemicals.

 

Application:

1-BROMOPENTANE is utilized in organic chemistry laboratories and industrial processes for reactions such as nucleophilic substitution and Grignard reactions. It is employed in the synthesis of pharmaceuticals, fragrances, and agricultural chemicals.

 

 

Articles:

- Phase transfer catalysed alkylation of 2′-hydroxy acetophenone with 1-bromopentane: Kinetics and mechanism of liquid–liquid reaction

Publication Date: Available online 3 October 2005

Ganapati D. Yadav, Neesha M. Desai

https://doi.org/10.1016/j.molcata.2005.08.029

 

- Identification of glutathione conjugates of 1-bromopentane and its hepatotoxicity in female BALB/c mice

Publication Date: 29 October 2008

Sang Kyu Lee, Dong Ju Lee, Hye Hyun Yoo, Ju Hyun Kim, Young Min Seo, Sil Shin, Jae Ho Choi, Tae Won Jeon, Mi Jeong Kang & Tae Cheon Jeong

https://doi.org/10.1007/s12272-001-2112-3

 

- Enhancing Moisture Stability of Sulfide Solid-State Electrolytes by Reversible Amphipathic Molecular Coating

Publication Date: July 11, 2022

Zhaoxin Yu, Shun-Li Shang, Kiseuk Ahn, Daniel T. Marty, Ruozhu Feng, Mark H. Engelhard, Zi-Kui Liu and Dongping Lu

https://doi.org/10.1021/acsami.2c07388