Organic lithium salts
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Filtered Search Results
Lithium Bis(pentafluoroethanesulfonyl)imide 98.0+%, TCI America™
CAS: 132843-44-8 Molecular Formula: C4F10LiNO4S2 Molecular Weight (g/mol): 387.09 MDL Number: MFCD22374096 InChI Key: ACFSQHQYDZIPRL-UHFFFAOYSA-N Synonym: Bis(pentafluoroethanesulfonyl)imide Lithium Salt PubChem CID: 12096715 IUPAC Name: lithium(1+) 1,1,1,2,2-pentafluoro-2-{[(1,1,2,2,2-pentafluoroethanesulfonyl)azanidyl]sulfonyl}ethane SMILES: [Li+].FC(F)(F)C(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(F)(F)C(F)(F)F
| PubChem CID | 12096715 |
|---|---|
| CAS | 132843-44-8 |
| Molecular Weight (g/mol) | 387.09 |
| MDL Number | MFCD22374096 |
| SMILES | [Li+].FC(F)(F)C(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(F)(F)C(F)(F)F |
| Synonym | Bis(pentafluoroethanesulfonyl)imide Lithium Salt |
| IUPAC Name | lithium(1+) 1,1,1,2,2-pentafluoro-2-{[(1,1,2,2,2-pentafluoroethanesulfonyl)azanidyl]sulfonyl}ethane |
| InChI Key | ACFSQHQYDZIPRL-UHFFFAOYSA-N |
| Molecular Formula | C4F10LiNO4S2 |
Sigma Aldrich Lithium Acetate Anhydrous 99.9% Trace Metal Basis
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| Recommended Storage | Room Temperature |
|---|
Sigma Aldrich N-Butyllithium Solution
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| Linear Formula | CH3(CH2)3Li |
|---|---|
| CAS | 109-72-8 |
| Biological Activity | Central Nervous System |
| Molecular Weight (g/mol) | 64.06 g/mol |
| MDL Number | MFCD00009414 |
| Health Hazard 1 | UN3394 - class 4.2 - PG 1 - EHS - Organometallic substance, liquid, pyrophoric, water-reactive, HI: all (not BR) |
| Synonym | n-BuLi; Butyl lithium; Butyllithium solution; Lithium-1-butanide |
| Recommended Storage | 2°C to 8°C |
| Molecular Formula | C4H9Li |
| Density | 0.68 g/mL at 25°C |
Sigma Aldrich Bis(trifluoromethane)sulfonimide lithium salt
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
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| Percent Purity | ≥99.0% (19 F-NMR) |
|---|---|
| Linear Formula | CF3SO2NLiSO2CF3 |
| CAS | 90076-65-6 |
| Molecular Weight (g/mol) | 287.09 |
| MDL Number | MFCD00210017 |
| Synonym | LiTFSI; Bis(trifluoromethylsulfonyl)amine lithium salt; Lithium bistrifluoromethanesulfonimidate |
| Recommended Storage | Room Temperature |
| Molecular Formula | C2F6LiNO4S2 |
| EINECS Number | 415-300-0 |
| Melting Point | 234°C to 238°C (lit.) |
TARGETMOL CHEMICALS INC ALPHA-THUJONE 100MG
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Also available in 10 mg 25 mg 50 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. (alpha)-Thujone is an inhibitor of ACh with an IC50 value of 24.7uM. purity: 98%
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Strem, An Ascensus Company CAS# 594-19-4. 1mole. t-Butyllithium 16% in pentane (1-2M). MFCD00008795
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CAS# 594-19-4. 1mole. t-Butyllithium 16% in pentane (1-2M). MFCD00008795. Molecular Weight: 64.05. Molecular Formula: C4H9Li. Color/form: slightly cloudy liq. Strem# 93-0302. http://www.strem.com/catalog/v/93-0302/
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Cayman Chemical EthylR- 3-Hydroxybutyra 25g
A chiral starting material for the production of numerous biologically active compounds
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Medchemexpress LLC Lithium acetate dihy 1kg
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Lithium acetate dihydrate is a compound with a one-dimensional structure that has various applications in industries such as pharmaceuticals ceramics and research laboratories Lithium acetate dihydrate is often used as a source of lithium ions in chemical reactions and as a precursor in the synthesis of other lithium compounds[1]
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Medchemexpress LLC Lith-O-Asp | 881179-02-8 | 98.0% | 491.66 | 100 MG
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Lith-O-Asp is a sialyltransferase (ST) inhibitor with IC50s of 12-37 μM. It inhibits the activities of ST3Gal I, ST3Gal III, and ST6GalI, decreasing the expression of cell surface α-2,3- and α-2,6-sialylated antigens.
- Inhibits sialyltransferase (ST) activities with IC50 values ranging from 12 to 37 μM.
- Decreases the activity of both α-2,3- and α-2,6-sialyltransferases.
- Inhibits the transfer of sialic acids to targeted glycoproteins.
- Shows no apparent growth inhibition effect toward different cancer cell lines at tested doses.
- Leads to fewer lung metastases in treated mice.
- Decreases average tumor nodules per mouse in vivo.
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eMolecules METHYL R-3-HYDROXYBUTYRAT 5G
5000225305 METHYL R-3-HYDROXYBUTYRAT 5G
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Medchemexpress LLC Lithium acetate dihy 50g
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Lithium acetate dihydrate is a compound with a one-dimensional structure that has various applications in industries such as pharmaceuticals ceramics and research laboratories Lithium acetate dihydrate is often used as a source of lithium ions in chemical reactions and as a precursor in the synthesis of other lithium compounds[1]
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TARGETMOL CHEMICALS INC COLUMBIN 50MG
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Also available in 5 mg 10 mg 25 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. 1. Columbin has anti-inflammatory activity. 2. Columbin has chemopreventive ability against human colon cancer. 3. Columbin inhibits PLA2 hydrolysis of ghost RBC in a dose-dependent fashion. purity: 99%
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Medchemexpress LLC Mevalonic acid lithium salt | 2618458-93-6 | 98.0% | 154.09 | 10 MG
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Mevalonic acid (MVA) lithium salt is a precursor substance of the mevalonate pathway, which is essential for cell growth and proliferation. It is effective in inhibiting Simvastatin-induced decrease in C2C12 cell viability in vitro. Mevalonic acid lithium salt can be used in studies of myopathy and heart failure.
- Precursor substance of the mevalonate pathway.
- Essential for cell growth and proliferation.
- Effective in inhibiting Simvastatin-induced decrease in C2C12 cell viability in vitro.
- Can be used in studies of myopathy and heart failure.
- High purity.
- Available in solid and solution forms.
- Supported by multiple publications citing its use.
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Ambeed Lithiumacetate
Lithiumacetate, 546-89-4, 99%
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AdipoGen Bis(trifluoromethane)sulfonimide lithium salt
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Bis(trifluoromethane)sulfonimide lithium salt, AdipoGen Life Sciences. Chemical. CAS: 90076-65-6. Formula: C2F6LiNO4S2. MW: 287.09. Synthetic Used in the preparation of electrolyte suitable for lithium batteries showing very high conductivity. Used in the preparation of a chiral imidazolium salt via anion metathesis of the corresponding triflate.
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