n-ブチリチウム溶液 - 2.ヘキサン中7M(25%溶液) , CAS No.109-72-8

CAS: 109-72-8 Cat. No.: B107553 分子式: C4H9Li 分子量: 64.06 Beilstein Registry Number: 1209227 EC番号: 203-698-7
注文可能
GRADE & PURITY 2.7M in hexane(25% solution)
Synonyms
ブチルリチウム|リチウム-1-ブタニド|n-BuLi
Storage
2-8℃で保管、アルゴン充填
Shipped In
濡れた氷
★
Size
USA
ドイツ (EU)*
Price
Qty
100ml
B107553-100ml
4 在庫あり
—
$53.90
500ml
B107553-500ml
1 在庫あり
—
$208.90
Enter a quantity for the sizes you want to add.
🧪
Why this grade

2.ヘキサン中7M(25%溶液) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

2-8℃で保管、アルゴン充填 Ships 濡れた氷 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

同義語
ブチルリチウム|リチウム-1-ブタニド|n-BuLi
仕様と純度
2.ヘキサン中7M(25%溶液)
保管条件
2-8℃で保管、アルゴン充填
入荷
濡れた氷
名前と識別子
異性体SMILES
[Li+].CCC[CH2-]
WGKドイツ
2
UN番号
3394
包装グループ
I
分子量
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

証明書(CoA、COO、BSE/TSEと分析図)
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.

29 results found

Lot NumberCertificate Type日付商品
G2631175Certificate of AnalysisJul 25, 2026 B107553
G2631174Certificate of AnalysisJul 25, 2026 B107553
D2608149Certificate of AnalysisMar 30, 2026 B107553
D2608148Certificate of AnalysisMar 30, 2026 B107553
J2531488Certificate of AnalysisOct 25, 2025 B107553
J2531487Certificate of AnalysisOct 25, 2025 B107553
G2524204Certificate of AnalysisJun 28, 2025 B107553
G2524203Certificate of AnalysisJun 28, 2025 B107553
C2507255Certificate of AnalysisJan 06, 2025 B107553
C2507254Certificate of AnalysisJan 06, 2025 B107553
K2429223Certificate of AnalysisNov 07, 2024 B107553
K2429229Certificate of AnalysisNov 07, 2024 B107553
H2406293Certificate of AnalysisJul 29, 2024 B107553
H2406294Certificate of AnalysisJul 29, 2024 B107553
E2431106Certificate of AnalysisMay 22, 2024 B107553
E2431113Certificate of AnalysisMay 22, 2024 B107553
B2423165Certificate of AnalysisJan 10, 2024 B107553
B2423213Certificate of AnalysisJan 10, 2024 B107553
B2423167Certificate of AnalysisJan 10, 2024 B107553
B2423166Certificate of AnalysisJan 10, 2024 B107553
A2412046Certificate of AnalysisNov 28, 2022 B107553
L2216298Certificate of AnalysisNov 28, 2022 B107553
L2216299Certificate of AnalysisNov 28, 2022 B107553
I2209336Certificate of AnalysisAug 17, 2022 B107553
I2209337Certificate of AnalysisAug 17, 2022 B107553
H2204313Certificate of AnalysisJul 11, 2022 B107553
H2204314Certificate of AnalysisJul 11, 2022 B107553
C2226556Certificate of AnalysisMar 07, 2022 B107553
C2226554Certificate of AnalysisMar 07, 2022 B107553
化学的性質と物理的性質
感度Air & Moisture Sensitive,Heat sensitive
引火点(°F)10 °F
引火点(°C)-21℃
沸点(°C)80°C
融点(°C)-95 °C
よくある質問と記事
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
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