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| Product | Description | |
|---|---|---|
| 1, 1, 1-tri chlorotri fluoroethane | 1, 1, 1-tri chlorotri fluoroethane . Group: Biochemicals. Alternative Names: 1,1,1-Trifluoro-2,2,2-trichloroethane; 1, 1, 1-tri fluorotri chloroethane ; CFC 113a; F 113a; FC 113a; Freon 113a; Freon FT; R 113a. Grades: Highly Purified. CAS No. 354-58-5. Pack Sizes: 1g. Molecular Formula: C2Cl3F3, Molecular Weight: 187.38. US Biological Life Sciences. |  Worldwide |
| 1,?1-?Dichloro-?1-?fluoroethane | 1,?1-?Dichloro-?1-?fluoroethane is a chlorofluorocarbon affecting ozone levels and the stability of the atmosphere. It is a refrigerant used in cooling systems. Group: Biochemicals. Grades: Highly Purified. CAS No. 1717-00-6. Pack Sizes: 500mg, 2.5g. Molecular Formula: C2H3Cl2F, Molecular Weight: 116.95. US Biological Life Sciences. | Worldwide |
| 2-Fluoroethanol | 2-Fluoroethanol, is a highly toxic building block, used for the preparation of different chemicals. It can also be used as a rodenticide, insecticide, and acaricide. Group: Biochemicals. Grades: Highly Purified. CAS No. 371-62-0. Pack Sizes: 2.5g, 10 g. Molecular Formula: C2H5FO, Molecular Weight: 64.06. US Biological Life Sciences. | Worldwide |
| 2-Fluoroethylamine HydroChloride | 2-Fluoroethylamine HydroChloride. Group: Perovskite solar cell (psc) materials. Alternative Names: 2-Aminoethyl Fluoride HydroChloride; 2-Fluoroethylammonium HydroChloride. CAS No. 460-08-2. Product ID: 2-fluoroethanamine; hydrochloride. Molecular formula: 99.53 g/mol. Mole weight: C2H6FN HCl. C(CF)N.Cl. InChI=1S/C2H6FN.ClH/c3-1-2-4;/h1-2, 4H2;1H. YRRZGBOZBIVMJT-UHFFFAOYSA-N. >97.0%(T). |  |
| FMK | FMK is a potent, highly specific and irreversible ribosomal s6 kinase (RSK) inhibitor that covalently modifies the C-terminal kinase domain of RSK. Its IC50 value is 15 nM. It could prevent the activation of the N-terminal kinase domain of RSK by the C-terminal kinase domain, but does not affect the activity of the N-terminal domain. It binds in the CTKD ATP-binding site and inhibits RSK autophosphorylation at Ser386. It induces significant apoptosis in human FGFR3-expressing, t(4;14)-positive multiple myeloma cells. It is used to determine the role of RSK as a direct regulator of NHE1 phosphorylation and sarcolemmal NHE activity in this cell type, in response to 1-adrenergic stimulation. Uses: Fmk could prevent the activation of the n-terminal kinase domain of rsk by the c-terminal kinase domain, but does not affect the activity of the n-terminal domain. it is used to determine the role of rsk as a direct regulator of nhe1 phosphorylation and sarcolemmal nhe activity in this cell type, in response to 1-adrenergic stimulation. Synonyms: 1-[4-Amino-7-(3-hydroxypropyl)-5-(4-methylphenyl)-7H-pyrrolo[2,3-d]pyrimidin-6-yl]-2-fluoroethanone;RSK2 kinase inhibitor. Grades: >98%. CAS No. 821794-92-7. Molecular formula: C18H19FN4O2. Mole weight: 342.37. |  |
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