LN7140529
                    1.3Msolutioninheptane,SpcSeal , 594-19-4
                            Synonym(s):
Lithium-2-methyl-2-propanide;t-BuLi
                            
                        
                CAS NO.:594-19-4
Empirical Formula: C4H9Li
Molecular Weight: 64.06
MDL number: MFCD00008795
EINECS: 209-831-5
Update time: 2022-07-08
                    PRODUCT Properties
| Boiling point: | 36-40 °C | 
                                    
| Density | 0.69 g/mL at 20 °C | 
                                    
| vapor density | ~3 (vs air) | 
                                    
| Flash point: | 20 °F | 
                                    
| storage temp. | 2-8°C | 
                                    
| form | liquid | 
                                    
| color | slightly cloudy | 
                                    
| Sensitive | Air & Moisture Sensitive | 
                                    
| BRN | 3587204 | 
                                    
| Exposure limits | ACGIH: TWA 1000 ppm OSHA: TWA 1000 ppm(2950 mg/m3) NIOSH: IDLH 1500 ppm; TWA 120 ppm(350 mg/m3); Ceiling 610 ppm(1800 mg/m3)  | 
                                    
| InChI | InChI=1S/C4H9.Li/c1-4(2)3;/h1-3H3; | 
                                    
| InChIKey | BKDLGMUIXWPYGD-UHFFFAOYSA-N | 
                                    
| SMILES | C(C)(C)(C)[Li] | 
                                    
| CAS DataBase Reference | 594-19-4(CAS DataBase Reference) | 
                                    
| EPA Substance Registry System | Lithium, (1,1-dimethylethyl)- (594-19-4) | 
                                    
Description and Uses
tert-Butyllithium solution (tert-BuLi) is an organolithium compound, used as a strong base in organic chemistry. It facilitates lithium-halogen exchange reaction and also can be employed in the deprotonation of C-H compounds and amines. it has applications in organic synthesis since it is a strong base, capable of deprotonating many carbon molecules, including benzene. tert-Butyllithium is available commercially as hydrocarbon solutions; it is not usually prepared in the laboratory. Its synthesis was first reported by R. B. Woodward in 1941.
- There are no commercial uses of t-butyllithium, but it is used as a polymerization initiator and as a metalating agent in the laboratory.
 - Alkylating and metalating agent. Reagent for the introduction of the tert-butyl group.
 - tert-Butyllithium (t-BuLi) is the most reactive of the commercially available organolithium reagents. It is supplied as a standard solution in hydrocarbon solvents, usually in a bottle sealed with a septum.
 
Safety
| Symbol(GHS) | ![]() ![]() ![]() ![]() ![]() GHS02,GHS05,GHS07,GHS08,GHS09  | 
                                    
| Signal word | Danger | 
| Hazard statements | H252-H318-H225-H250-H260-H304-H314-H336-H410-H411 | 
| Precautionary statements | P301+P310a-P303+P361+P353-P305+P351+P338-P405-P422a-P501a-P210-P222-P223-P231+P232-P370+P378-P422 | 
| Hazard Codes | F,C,N | 
| Risk Statements | 11-15-17-34-51/53-65-66-67-50/53-38-14/15 | 
| Safety Statements | 26-36/37/39-43-45-62-61-16-33-9 | 
| RIDADR | UN 3394 4.2/PG 1 | 
| WGK Germany | 1 | 
| F | 3-10 | 
| TSCA | Yes | 
| HazardClass | 4.3 | 
| PackingGroup | I | 
| HS Code | 29319090 | 








