94439
tert-Butyllithium solution
1.6-3.2 M in heptane
Synonym(s):
Lithium-2-methyl-2-propanide, t-BuLi
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About This Item
Linear Formula:
(CH3)3CLi
CAS Number:
Molecular Weight:
64.06
UNSPSC Code:
12352103
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
3587204
Concentration:
1.6-3.2 M in heptane
Form:
solution
form
solution
Quality Level
shelf life
limited shelf life
concentration
1.6-3.2 M in heptane
density
0.69 g/mL at 20 °C
storage temp.
2-8°C
SMILES string
[Li]C(C)(C)C
InChI
1S/C4H9.Li/c1-4(2)3;/h1-3H3;
InChI key
BKDLGMUIXWPYGD-UHFFFAOYSA-N
General description
recommended storage temperature 15°C
Other Notes
decomp. rate (at room temperature) 0.02-0.1% per day
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signalword
Danger
target_organs
Central nervous system
Storage Class
4.2 - Pyrophoric and self-heating hazardous materials
wgk
WGK 2
flash_point_f
24.8 °F - closed cup
flash_point_c
-4.0 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Eye Dam. 1 - Flam. Liq. 2 - Pyr. Liq. 1 - Skin Corr. 1B - STOT SE 3 - Water-react. 1
Regulatory Information
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Xinyi Chia et al.
ACS nano, 9(5), 5164-5179 (2015-04-22)
Layered transition metal dichalcogenides (TMDs) have been the center of attention in the scientific community due to their properties that can be tapped on for applications in electrochemistry and hydrogen evolution reaction (HER) catalysis. We report on the effect of
Adeline Huiling Loo et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 16(11), 2304-2306 (2015-05-28)
Owing to the attractive properties that transition metal dichalcogenides (TMDs) display, they have found recent application in the fabrication of biosensing devices. These devices involve the immobilization of a recognition element such as DNA onto the surface of TMDs. Therefore
Shigeo Hayashi et al.
Journal of enzyme inhibition and medicinal chemistry, 29(6), 846-867 (2014-02-13)
Because of the pivotal role of cyclooxygenase (COX) in the inflammatory processes, non-steroidal anti-inflammatory drugs (NSAIDs) that suppress COX activities have been used clinically for the treatment of inflammatory diseases/syndromes; however, traditional NSAIDs exhibit serious side-effects such as gastrointestinal damage
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 724289-1G | 04061825592824 |
| 94439-100ML-F | 04061833292006 |
| 94439-PZ-F | 04061823824798 |