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  4. Oleyl bromide

Oleyl bromide  (Synonyms: (Z)-1-Bromooctadec-9-ene)

Cat. No.: HY-W011238
Handling Instructions Technical Support

Oleyl bromide ((Z)-1-Bromooctadec-9-ene) is a hydrophobic compound that can carry out ring-opening reaction through a process called "encapsulation". Oleyl bromine can also be used as the starting material in the synthesis of oleylphosphonates.

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Oleyl bromide Chemical Structure

Oleyl bromide Chemical Structure

CAS No. : 6110-53-8

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Oleyl bromide Related Antibodies

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Description

Oleyl bromide ((Z)-1-Bromooctadec-9-ene) is a hydrophobic compound that can carry out ring-opening reaction through a process called "encapsulation". Oleyl bromine can also be used as the starting material in the synthesis of oleylphosphonates.

Molecular Weight

331.37

Formula

C18H35Br
CAS No.
Appearance

Liquid

SMILES

BrCCCCCCCC/C=C\CCCCCCCC
Shipping

Room temperature in continental US; may vary elsewhere.
Storage
Pure form -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
Purity & Documentation
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Oleyl bromide Related Classifications

  • Molarity Calculator

  • Dilution Calculator

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass   Concentration   Volume   Molecular Weight *
= × ×

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
× = ×
C1   V1   C2   V2
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Keywords:

Oleyl6110-53-8(Z)-1-Bromooctadec-9-eneBiochemical Assay ReagentsInhibitorinhibitorinhibit

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