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1-Bromoheptane / 500 G

Purity: 99 %
Synonym: Heptyl bromide; n-Heptyl bromide; 1-bromo-heptane; 1-bromanylheptane
Molecular Formula: CH3(CH2)6Br
Molecular Weight: 179.10
SKU: MND-78257
CAS Number: 629-04-9
MDL number: MFCD00000273
EC Number: 211-068-8
Form: liquid
Note: Prices are for comparison only. Contact Sales for current pricing.
Packing size: 500 G  
51.80 EUR



Safety Information


Hazard Statements

H315
H319
H226

Precautionary Statements

P210
P280
P303 + P361 + P353
P264
P501
P305 + P351 + P338
P233
P240
P241
P242
P302 + P352
P403 + P235
P362 + P364
P243
P370 + P378
P321
P264 + P265
P332 + P317
P337 + P317

Pictograms



Properties

Signal WordWarning
Flash Point (C)60 °C - closed cup
Flash Point (F)140.0 °F - closed cup
Vapor Density6.18 (vs air)
Density1.14 g/mL at 25 °C (lit.)
Boiling Point180 °C (lit.)
Melting Point−58 °C (lit.)

 Product Description

1-Bromoheptane is an organic halide with a bromine atom attached to the first carbon of a heptane chain. It is commonly used in organic synthesis.

 

Application:

1-Bromoheptane is used as an alkylating agent in organic synthesis, facilitating the introduction of heptyl groups into various chemical compounds.

 

 

Articles:

- Application of a low power/reduced pressure helium ICP ionization source for mass spectrometric detection of organobromine compounds and derivatized organotin compounds

Publication Date: 7th January 2000

Joseph W. Waggoner, Lisa S. Milstein, Mikhail Belkin, Karen L. Sutton, Joseph A. Caruso and Harry B. Fannin

https://doi.org/10.1039/A905906G

 

- Protective effect of NAC against malathion-induced oxidative stress in freshly isolated rat hepatocytes

Publication Date: 2012 Mar 15

Sara Mostafalou, Mohammad Abdollahi, Mohammad Ali Eghbal and Nazli Saeedi Kouzehkonani

https://doi.org/10.5681%2Fapb.2012.011

 

- Synthesis and evaluation of quinonoid compounds against tumor cell lines

Publication Date: Available online 9 November 2010

Eufrânio N. da Silva Jr., Bruno C. Cavalcanti, Tiago T. Guimarães, Maria do Carmo F.R. Pinto, Igor O. Cabral, Cláudia Pessoa, Letícia V. Costa-Lotufo, Manoel O. de Moraes, Carlos K.Z. de Andrade, Marcelo R. dos Santos, Carlos A. de Simone, Marilia O.F. Goulart, Antonio V. Pinto

https://doi.org/10.1016/j.ejmech.2010.11.006