Lithium tert-butoxide solution - 1.0 M in THF , CAS No.1907-33-1

CAS: 1907-33-1 Cat. No.: L432264 Peso molecular: 80.05 Beilstein Registry Number: 3620018 Número EC: 217-611-5
Disponible para pedir
GRADE & PURITY 1.0 M in THF
Synonyms
lithium tbutoxide | lithium t-butoxide | lithium(1+) ion 2-methylpropan-2-olate | LiOtBu | 2-Methyl-2-propanol lithium salt | lithium tertbutoxide | Lithium tert-butoxide | Tussol: | L0253 | Lithium t-butoxide, 1M in THF | Lithium tert -butanolate | lithi
Storage
Room temperature
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Size
Estado
Price
Qty
50ml
L432264-50ml
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

112,90US$

132,90US$
Guardar 20,00 US$ (15.05%)
250ml
L432264-250ml
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

386,90US$

452,90US$
Guardar 66,00 US$ (14.57%)
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Why this grade

1.0 M in THF for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships Check lot-specific COA for exact specifications.

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Quality documents

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

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Literature proof

Cited in 8 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Application

Lithium tert -butoxide solution is generally used as a strong base in organic synthesis. It can be used: For the synthesis of lithium modified silica nano-particles for conductive gel electrolytes. As a catalyst for ring-opening polymerization of lactides. As a lithium precursor for the synthesis of LiV 3 O 8 nanoparticles by flame spray pyrolysis.

Specifications

Sinónimos
lithium tbutoxide | lithium t-butoxide | lithium(1+) ion 2-methylpropan-2-olate | LiOtBu | 2-Methyl-2-propanol lithium salt | lithium tertbutoxide | Lithium tert-butoxide | Tussol: | L0253 | Lithium t-butoxide, 1M in THF | Lithium tert -butanolate | lithi
Especificaciones y pureza
1.0 M in THF
Condiciones de almacenamiento de almacenamiento
Room temperature
Nombres e identificadores
Sonrisas canónicas[Li+].CC(C)(C)[O-]
IUPAC Namelithium;2-methylpropan-2-olate
InChIKeyLZWQNOHZMQIFBX-UHFFFAOYSA-N
INCHI1S/C4H9O.Li/c1-4(2,3)5;/h1-3H3;/q-1;+1
Isómeros SMILES [Li+].CC(C)(C)[O-]
WGK Alemania 3
Número ONU 3206
Grupo de embalaje II
Peso molecular 80.05
Beilstein 3620018
Reaxy-Rn 8541101
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=8541101&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

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic salts
ClaseOrganic metal salts
SubclassOrganic alkali metal salts
Intermediate Tree Nodes Not available
Direct ParentOrganic lithium salts
Alternative Parents Organic zwitterions  Organic oxides  Hydrocarbon derivatives  Alkoxides  
Molecular FrameworkAliphatic acyclic compounds
Substituents Organic lithium salt - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic zwitterion - Alkoxide - Organooxygen compound - Aliphatic acyclic compound
DescripciónThis compound belongs to the class of organic compounds known as organic lithium salts. These are organic compounds containing a lithium ion.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
Punto de inflamación (°F)-18.4 °F
Punto de inflamación (°C)-28 °C
Punto de ebullición (°C)110 °C/at 0.1333 hPa
Peso molecular80.100 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Exact Mass80.0813 Da
Monoisotopic Mass80.0813 Da
Topological Polar Surface Area23.100 Ų
Heavy Atom Count6
Formal Charge0
Complexity29.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
Citations of This Product
Referencias
1. Jiabin Fang, Jianguo Li, Lijun Qin, Aidong Li, Hao Feng.  (2023)  Atomic/Molecular Layer-Deposited Laminated Li2O–Lithicone Interfaces Enabling High-Performance Silicon Anodes.  ACS Applied Materials & Interfaces,      [PMID:37256652] [10.1021/acsami.3c02925]
2. Muhammad Irfan, Yuli Zang, Zeheng Yang, Weixin Zhang.  (2023)  Hydrophobicity of 2-((8-hydroxyoctyl)oxy)ethyl-sulfanetrione in conducting solid polymer electrolyte boosting the electrochemical performance of lithium metal batteries.  JOURNAL OF POWER SOURCES,      [PMID:] [10.1016/j.jpowsour.2023.233206]
3. Yunlong Zhang, Muhammad Irfan, Zeheng Yang, Kun Liu, Jianhui Su, Weixin Zhang.  (2022)  Lithium hydroxyphenyl propanesulfonate imparts composite solid polymer electrolytes with ultrahigh ionic conductivity for dendrite free lithium batteries.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2022.134775]
4. Zifeng Yang, Lei Liu, Hongzhe An, Chenhao Li, Zhencai Zhang, Wenjuan Fang, Fei Xu, Suojiang Zhang.  (2020)  Cost-Effective Synthesis of High Molecular Weight Biobased Polycarbonate via Melt Polymerization of Isosorbide and Dimethyl Carbonate.  ACS Sustainable Chemistry & Engineering,      [PMID:] [10.1021/acssuschemeng.0c00430]
5. Ru-Jun Chen, Yi-Bo Zhang, Ting Liu, Bing-Qing Xu, Yang Shen, Yuan-Hua Lin, Ce-Wen Nan.  (2017)  Improvement of the conductivity of sol-gel derived Li-La-Zr-O thin films by the addition of surfactant.  CERAMICS INTERNATIONAL,      [PMID:] [10.1016/j.ceramint.2017.05.201]
6. Ru-Jun Chen, Mian Huang, Wen-Ze Huang, Yang Shen, Yuan-Hua Lin, Ce-Wen Nan.  (2014)  Sol–gel derived Li–La–Zr–O thin films as solid electrolytes for lithium-ion batteries.  Journal of Materials Chemistry A,  (33): (13277-13282).  [PMID:] [10.1039/C4TA02289K]
7. Ping Sun, Li Huang, Zimu Li, Yao Yang, Shiman Lu, Nansha Gao, Hongzhong Chen, Xiaowei Zeng, Zhongjian Xie.  (2024)  Charge-reversal biodegradable nanoplatform with ferroptosis and ICD induction for tumor synergistic treatment.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2024.149234]
8. Jiabin Fang, Kang Wu, Lijun Qin, Jianguo Li, Wangle Zhang, Ting Gong, Hao Feng.  (2025)  Atomic Layer Deposited Silicon Anode with Nanoporous Fluorinated Surface Modulation Enabling Invertible Electrochemical Lithium Storage.  Small,      [PMID:40630042] [10.1002/smll.202504940]
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