Skip to Content
Merck
All Photos(1)

Documents

939412

Sigma-Aldrich

n-Butyllithium solution

new

2.5 M (in PAO/hexanes mixture)

Synonym(s):

Butyllithium solution, Lithium-1-butanide, n-BuLi, Butyl lithium

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3(CH2)3Li
CAS Number:
Molecular Weight:
64.06
Beilstein:
1209227
MDL number:
UNSPSC Code:
12352142

form

liquid

Quality Level

concentration

2.5 M (in PAO/hexanes mixture)

color

colorless to yellow

storage temp.

2-8°C

SMILES string

[Li]CCCC

InChI

1S/C4H9.Li/c1-3-4-2;/h1,3-4H2,2H3;

InChI key

MZRVEZGGRBJDDB-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

n-Butyllithium (n-BuLi) is an organolithium reagent commonly used as a strong base in organic synthesis. It is also used as a lithium source for a wide range of lithium bases, such as lithium amides, acetylides, and alkoxides.

Application

n-BuLi can be used as a strong base to form corresponding lithium salts by the deprotonation of nitrogen, oxygen, phosphorus, and carbon acids. Heterocyclic compounds, such as furans, thiophenes, oxazoles, pyrroles, etc, can be lithiated α to the ring heteroatom using n-BuLi. These lithiated salts react in situ with alkyl halides to obtain useful organic compounds by the formation of the C-C bond. n-BuLi is also a useful reagent for lithium–halogen exchange reactions. Synthesis of various other useful reagents such as lithium diisopropylamide (LDA) and diphenylphosphine is done by in situ reaction with n-BuLi In the polymerization of dienes, n-BuLi is employed as an initiator.




The product is also used in the following reactions:

  • Anionic rearrangement reactions
  • Metal-halogen interchange and transmetalation reactions
  • Elimination reactions
  • [1,2]- and [1,4]-Wittig rearrangement reaction
  • Anionic homo-Fries rearrangement reaction
  • Asymmetric carbolithiation

Features and Benefits

This product is formulated in a solution of polyalphaolefin (PAO) and hexanes to prevent pyrophoric reactions when exposed to air, affording improved safety and usability.

related product

Product No.
Description
Pricing

Signal Word

Danger

Hazard Classifications

Aquatic Chronic 3 - Asp. Tox. 1 - Eye Dam. 1 - Flam. Liq. 3 - Pyr. Liq. 1 - Repr. 2 - Skin Corr. 1B - STOT RE 2 Inhalation - Water-react 1

Target Organs

Nervous system

Supplementary Hazards

Storage Class Code

4.2 - Pyrophoric and self-heating hazardous materials

WGK

WGK 3

Flash Point(F)

88.7 °F

Flash Point(C)

31.5 °C


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Articles

Transformative reagents enable selective conversions within molecules containing sensitive functionalities under mild reactions.

Transformative reagents enable selective conversions within molecules containing sensitive functionalities under mild reactions.

Transformative reagents enable selective conversions within molecules containing sensitive functionalities under mild reactions.

Transformative reagents enable selective conversions within molecules containing sensitive functionalities under mild reactions.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service