20159
正丁基锂 溶液
2.7 M in heptane
别名:
1-丁基锂, n-BuLi, Butyl lithium, 丁基锂 溶液
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关于此项目
线性分子式:
CH3(CH2)3Li
化学文摘社编号:
分子量:
64.06
UNSPSC Code:
12352103
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1209227
Concentration:
2.7 M in heptane
Form:
liquid
InChI
1S/C4H9.Li/c1-3-4-2;/h1,3-4H2,2H3;
SMILES string
[Li]CCCC
InChI key
MZRVEZGGRBJDDB-UHFFFAOYSA-N
form
liquid
shelf life
limited shelf life
concentration
2.7 M in heptane
color
yellow
density
0.71 g/mL at 20 °C
storage temp.
2-8°C
Quality Level
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Application
n-Butyllithium is a strong nucleophile in the synthetic organic chemistry. It is also used as an initiator in the polymerization process.
Disclaimer
长时间储存可形成氢化锂沉淀
signalword
Danger
hcodes
target_organs
Central nervous system
supp_hazards
存储类别
4.2 - Pyrophoric and self-heating hazardous materials
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3 - Water-react. 1
法规信息
新产品
此项目有
Methylsulfinyl carbanion (CH3-SO-CH2-). Formation and applications to organic synthesis
Corey EJ and Chaykovsky M
Journal of the American Chemical Society, 87(6), 1345-1353 (1965)
Some trends observed in [60] fullerene polymerization activated by butyllithium isomers
Atovmyan EG, et al.
Russian Chemical Bulletin, 61(11), 2178-2179 (2012)
Tatiana Guzzo et al.
Biomolecules, 10(11) (2020-10-30)
The stability and the degradation of polymers in physiological conditions are very important issues in biomedical applications. The copolymer of hyaluronic acid and poly-D,L-lactic acid (made available in a product called DAC®) produces a hydrogel which retains the hydrophobic character
Jennifer L Rutherford et al.
Journal of the American Chemical Society, 124(2), 264-271 (2002-01-10)
6Li and (13)C NMR spectroscopic studies were carried out on [(6)Li]n-BuLi and [(6)Li]PhLi (RLi) in toluene-d(8) containing the following diamines: N,N,N',N'-tetramethylethylenediamine (TMEDA), N,N,N',N'-tetraethylethylenediamine, 1,2-dipyrrolidinoethane, 1,2-dipiperidinoethane, N,N,N',N'-tetramethylpropanediamine, trans-(R,R)-N,N,N',N'-tetramethylcyclohexanediamine, and (-)-sparteine. Dimers of general structure (RLi)(2)S(2) (S = chelating diamine) are formed
Deyu Li et al.
The Journal of organic chemistry, 73(6), 2373-2381 (2008-02-26)
A system consisting of a chiral lithium amide and n-BuLi in tol-d(8) solution was investigated with (1)H and (13)C INEPT DOSY, (6)Li and (15)N NMR, and other 2D NMR techniques. A mixed 2:1 trimeric complex was identified as the major
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