n-Butyllithium solution - 2.0 M in cyclohexane , CAS No.109-72-8

CAS: 109-72-8 Cat. No.: N431407 Formule: C4H9Li Poids moléculaire: 64.06 Beilstein Registry Number: 1209227 Numéro CE: 203-698-7
DISPONIBLE À COMMANDE
GRADE & PURITY 2.0 M in cyclohexane
Synonyms
Butyl lithium, Lithium-1-butanide, Butyllithium solution, n-BuLi
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice,FedEx DG Service
★
Size
Allemagne (EU)
USA*
Price
Qty
25ml
N431407-25ml
—
2 En stock

74,54€

87,55€
Enregistrer 13,02 € (14.87%)
100ml
N431407-100ml
—
1 En stock

176,93€

212,51€
Enregistrer 35,58 € (16.74%)
4×25ml
N431407-4×25ml
Sur commande · 8–12 semaines

179,54€

253,29€
Enregistrer 73,76 € (29.12%)
Enter a quantity for the sizes you want to add.
🧪
Why this grade

2.0 M in cyclohexane for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Argon charged Ships Wet ice,FedEx DG Service Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 123 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonymes
Butyl lithium, Lithium-1-butanide, Butyllithium solution, n-BuLi
Spécifications et pureté
2.0 M in cyclohexane
Conditions de stockage de stockage
Store at 2-8°C,Argon charged
Expédié en
Wet ice,FedEx DG Service
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Noms et identifiants
Isomères SMILES
[Li+].CCC[CH2-]
WGK Allemagne
2
Numéro ONU
3394
Groupe d'emballage
I
Poids moléculaire
64.06
Beilstein
1209227
Reaxy-Rn
1209227
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1209227&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

8 results found

Lot NumberCertificate TypeDateArticle
L2314292Certificate of AnalysisSep 07, 2026 N431407
L2314293Certificate of AnalysisSep 07, 2026 N431407
G2616526Certificate of AnalysisJul 08, 2026 N431407
G2616531Certificate of AnalysisJul 08, 2026 N431407
L2504523Certificate of AnalysisNov 26, 2025 N431407
L2504532Certificate of AnalysisNov 26, 2025 N431407
C2513596Certificate of AnalysisMar 06, 2025 N431407
C2513601Certificate of AnalysisMar 06, 2025 N431407
Propriétés chimiques et physiques
Point d'éclair (°F)10 °F
Point d'éclair (°C)-21℃
Point d'ébullition (°C)80°C
Point de fusion (°C)-95 °C
FAQ et articles
Pinacolborane
OSF/ASF Dual-Channel Toolbox: Divergent Reactions of Four-Membered Ring Sulfonyl Fluorides, Condition “Knobs,” and Selection Navigation
How to Make Organolithium Reactions Reproducible: Lock Down the Effective Equivalents, Aggregation State, and the Addition/Temperature-Control Window
Experimental Selection of SEM-Cl: From O/N-SEM Protection and Directed Functionalization of N-Heterocycles to the Introduction of Protected C1 Fragments
Experimental Selection Logic for C-C Bond Construction: Understanding Fragment Coupling, Carbonyl Chain Extension, Olefination, and Late-Stage Bond-Forming Pathways by Bond-Forming Task
From Nucleophilic to Electrophilic BCB Synthetic Equivalents: Hypervalent-Iodine-Mediated Umpolung Design
One-Pot Arylation of the Piperidine α-C–H Bond: From Directed Lithiation and Li→Zn Transmetalation to Negishi Coupling
Where Does the Selectivity in Piperidine C–H Functionalization Come From? — Nitrogen Effects, Chair Conformations, and Four Classes of Key Intermediates
3,3-Spiro-α-Proline Building Blocks: Structural Features, Complementary Synthetic Routes, and Multigram-Scale Preparation
Direct Construction of Methylsulfonyl-Containing Heterocycles: Synthesis and Applications of Prefunctionalized Three-Carbon Vinamidinium Salts
Regioselective Deprotonative Metalation of Pyridines: C–H Acidity, Coordination Effects, and Metal Systems
Citations of This Product
Calculateurs de solution
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