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Merck

230715

Sigma-Aldrich

丁基锂 溶液

11.0 M in hexanes

别名:

1-丁基锂, n-BuLi, Butyl lithium, 丁基锂 溶液

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About This Item

线性分子式:
CH3(CH2)3Li
CAS号:
分子量:
64.06
Beilstein:
1209227
MDL號碼:
分類程式碼代碼:
12352103
PubChem物質ID:
NACRES:
NA.22

形狀

liquid

品質等級

濃度

11.0 M in hexanes

密度

0.761 g/mL at 25 °C

儲存溫度

2-8°C

SMILES 字串

[Li]CCCC

InChI

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

InChI 密鑰

MZRVEZGGRBJDDB-UHFFFAOYSA-N

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一般說明

n-Butyllithium (n-BuLi) is an organolithium reagent commonly 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 reacting in situ with alkyl halides to obtain useful organic compounds by the formation of the C-C bond.

應用

n-BuLi can be used as a reagent for lithium-halogen exchange reactions. Synthesis of various other useful reagents such as lithium diisopropylamide (LDA) and diphenylphosphine is prepared by in situ reaction with n-BuLi . In the polymerization of dienes, it can be employed as an initiator.

包裝

The 25 mL Sure/Seal bottle is recommended as a single-use bottle. Repeated punctures will likely result in decreased performance of product.

法律資訊

Sure/Seal is a trademark of Sigma-Aldrich Co. LLC

訊號詞

Danger

危險分類

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

標靶器官

Central nervous system, Nervous system

安全危害

儲存類別代碼

4.2 - Pyrophoric and self-heating hazardous materials

水污染物質分類(WGK)

WGK 3

閃點(°F)

-7.6 °F - closed cup

閃點(°C)

-22 °C - closed cup

個人防護裝備

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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其他客户在看

n-Butyllithium.
eEROS (Encyclopedia of Reagents for Organic Synthesis) (2001)
Preparation, Properties, and Safe Handling of Commercial Organolithiums: Alkyllithiums, Lithium sec-Organoamides, and Lithium Alkoxides.
Rathman, Terry `Li? and Schwindeman, James A
Organic Process Research & Development, 18(10), 1192-1210 (2014)
n-Butyllithium
Ovaska TV, et al.
Encyclopedia of Reagents for Organic Synthesis, Second Edition (2001)
Microstructure-thermal property relationship of high trans-1, 4-poly (butadiene) produced by anionic polymerization of 1, 3-butadiene using an initiator composed of alkyl aluminum, n-butyl lithium, and barium alkoxide
Benvenuta-Tapia JJ, et al.
Polym. Eng. Sci., 49(1), 1-10 (2009)
Rhodium pincer complexes of 2, 2?-bis (diphenylphosphino) diphenylamine
Winter AM, et al.
Journal of Organometallic Chemistry, 682(1-2), 149-154 (2003)

商品

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.

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