Tartaric Acid
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Sigma Aldrich DL-Tartaric acid
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% |
|---|---|
| Linear Formula | HOOC(CHOH)2 COOH |
| CAS | 133-37-9 |
| Molecular Weight (g/mol) | 150.09 |
| MDL Number | MFCD00071626 |
| Synonym | DL-2,3-Dihydroxybutanedioic acid |
| Recommended Storage | Room Temperature |
| Molecular Formula | C4H6O6 |
| EINECS Number | 205-105-7 |
| Melting Point | 210°C to 212°C (lit.) |
Sigma Aldrich meso-Tartaric acid monohydrate
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 | ≥97% |
|---|---|
| Linear Formula | C4H6O6 -+ H2O |
| CAS | 5990-63-6 |
| Molecular Weight (g/mol) | 168.1 |
| MDL Number | MFCD00150742 |
| Synonym | Mesotartaric acid |
| Recommended Storage | Room Temperature |
| Molecular Formula | C4H6O6 -+ H2O |
| EINECS Number | 205-696-1 |
| Melting Point | 165°C to 166°C (anhydrous) (lit.) |
Sigma Aldrich D-(-)-Tartaric Acid
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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| Synonym | (2S,3S)-(-)-Tartaric acid; D-Threaric acid |
|---|
eMolecules (+)-Diacetyl-d-tartaric acid | 66749-60-8 | MFCD02093460 | 1g
Combi-Blocks | (+)-Diacetyl-d-tartaric acid | 1g | 495744747 | QG-6219 | 95.000 | 66749-60-8 | MFCD02093460 | 234.160 | C8H10O8
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eMolecules (-)-Diacetyl-l-tartaric acid | 51591-38-9 | MFCD00070579 | 1g
Combi-Blocks | (-)-Diacetyl-l-tartaric acid | 1g | 342866128 | QE-6168 | 95.000 | 51591-38-9 | MFCD00070579 | 234.160 | C8H10O8
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eMolecules (+)-L-Tartaric acid dibenzyl amide | 88393-56-0 | MFCD00064478 | 25g
Combi-Blocks | (+)-L-Tartaric acid dibenzyl amide | 25g | 415498019 | QC-5794 | 98.000 | 88393-56-0 | MFCD00064478 | 328.368 | C18H20N2O4
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eMolecules L-(+)-Tartaric acid di-n-butyl ester | 87-92-3 | MFCD00009443 | 1g
Combi-Blocks | L-(+)-Tartaric acid di-n-butyl ester | 1g | 374521995 | QE-7161 | 95.000 | 87-92-3 | MFCD00009443 | 262.302 | C12H22O6
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Medchemexpress LLC Fostamatinib (disodium hexahydrate) | 914295-16-2 | 99.5% | 25 MG
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Fostamatinib (disodium hexahydrate) is a laboratory chemical provided as a solid with a purity of 99.5%. It requires sealed storage at 4°C away from moisture. When in solvent, it can be stored at -80°C for 6 months or -20°C for 1 month.
- Stable under recommended storage conditions
- Requires sealed storage to protect from moisture
- Recommended storage at 4°C
- For solutions, store at -80°C (up to 6 months) or -20°C (up to 1 month)
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Medchemexpress LLC Prednisolone disodium phosphate | 125-02-0 | MFCD00083682 | 99.50% | 25 MG
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Prednisolone disodium phosphate is a synthetic glucocorticoid with anti-inflammatory and immunomodulating properties. It is rapidly and completely hydrolyzed into prednisolone in the plasma. This product is intended for research use only.
- Synthetic glucocorticoid
- Possesses anti-inflammatory properties
- Has immunomodulating properties
- Rapidly and completely hydrolyzed into prednisolone in plasma
- White to off-white solid appearance
- Molecular weight of 484.39
- Chemical formula C21H27Na2O8P
- Recommended storage at 4°C, sealed and away from moisture
- In solution, can be stored at -80°C for 6 months or -20°C for 1 month
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Medchemexpress LLC ENMD-2076 | 934353-76-1 | 99.99% | 375.47 | 10 MG
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ENMD-2076 is a multi-targeted kinase inhibitor, demonstrating significant activity against Aurora A, Flt3, KDR/VEGFR2, and other kinases. It effectively inhibits cellular autophosphorylation and induces G2-M-phase arrest and apoptosis in various cell lines. In vivo studies show dose-dependent inhibition of tumor growth and tumor regression, with the compound being well tolerated.
- Inhibits multiple kinases including Aurora A, Flt3, VEGFR2
- Induces G2-M-phase arrest and apoptosis
- Demonstrates antiproliferative activity against human cell lines
- Inhibits cellular Flt3 ligand (FL)-induced Flt3 autophosphorylation
- Inhibits stem cell factor (SCF)-induced Kit autophosphorylation
- Inhibits VEGFR2/KDR autophosphorylation
- Leads to dose-dependent inhibition of tumor growth in vivo
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Medchemexpress LLC ENMD-2076 | 934353-76-1 | 99.99% | 375.47 | 100 MG
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ENMD-2076 is a multi-targeted kinase inhibitor with high selectivity towards Aurora A versus Aurora B. It inhibits HUVEC growth and shows antiproliferative effects on human leukemia cell lines. This compound induces G2-M-phase arrest and apoptosis in U937 cells and inhibits Flt3 and Kit autophosphorylation. In vivo, ENMD-2076 demonstrates dose-dependent inhibition of tumor growth and is well tolerated in animal studies.
- Multi-targeted kinase inhibitor.
- Inhibits HUVEC growth.
- Shows antiproliferative effects on leukemia cell lines.
- Induces G2-M-phase arrest and apoptosis.
- Inhibits Flt3 ligand (FL)-induced Flt3 autophosphorylation.
- Inhibits stem cell factor (SCF)-induced Kit autophosphorylation.
- Inhibits VEGFR2/KDR autophosphorylation.
- Results in dose-dependent inhibition of tumor growth in vivo.
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Medchemexpress LLC ENMD-2076 Tartrate | 1453868-32-0 | 99.7% | 525.56 | 10 MG
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ENMD-2076 Tartrate is a multi-targeted kinase inhibitor with IC50s of 1.86, 14, 58.2, 15.9, 92.7, 70.8, 56.4 nM for Aurora A, Flt3, KDR/VEGFR2, Flt4/VEGFR3, FGFR1, FGFR2, Src, PDGFRα, respectively. It is for research use only and not sold to patients.
- Acts as a multi-targeted kinase inhibitor
- Inhibits Aurora A, Flt3, KDR/VEGFR2, Flt4/VEGFR3, FGFR1, FGFR2, Src, and PDGFRα
- Shows selective inhibition of Aurora A over Aurora B
- Inhibits human umbilical vein endothelial cell (HUVEC) growth
- Blocks cellular Flt3 ligand (FL)-induced Flt3 autophosphorylation
- Prevents stem cell factor (SCF)-induced Kit autophosphorylation
- Inhibits VEGFR2/KDR autophosphorylation
- Demonstrates dose-dependent inhibition of tumor growth or tumor regression in vivo
- Exhibits good tolerance in daily doses during in vivo studies
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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