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| Product | Description | |
|---|---|---|
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| Weat Gluten Processing Complex Enzyme (Food Grade) | This product is a compound enzyme which designed for the processing of weat gluten. Applications: 1.influencing on the non-starch polysaccharides(nps) ,the viscosity of starches is increased. 2.increase the yield of starches and vital wheat glutens. 3.reduce the consumption of materials,water and energy. Group: Enzymes. Synonyms: Wheat Gluten Processing Complex Enzyme; Complex Enzyme; Wheat Gluten Processing; starch processing enzymes; starch; Wheat Gluten; Food Grade. Starch enzyme. Activity: 8,000,000u/ml. Storage: Should be stored in a cool place avoiding high temperature. Liquid: 3 months at 25°C, activity remain >90%; 6 months, activity remains >80%. Increase dosage after shelf life. Form: Liquid. Wheat Gluten Processing Complex Enzyme; Complex Enzyme; Wheat Gluten Processing; starch processing enzymes; starch; Wheat Gluten; Food Grade. Pack: 25kgs/drum, 1.125kgs/drum. Cat No: ASE-001. |  |
| WEB2086 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| WEB 2086 | WEB 2086. Group: Biochemicals. Grades: Purified. CAS No. 105219-56-5. Pack Sizes: 1mg, 10mg. US Biological Life Sciences. |  Worldwide |
| WEB 2086 | WEB 2086 is a potent and selective platelet-activating factor (PAF) receptor antagonist (Ki = 16.3 nM) potentially used for the treatment of asthma and allergic rhinitis (AR). WEB 2086 exhibits an inhibitory effect on growth and proliferation of MCF-7 breast cancer cells. Uses: Platelet aggregation inhibitors. Synonyms: DE-081; DE 081; DE081; WEB-2086; WEB2086; WEB2086; WEB-2086BS; Apafant. Apafant; 4-[3-[4[(2-Chlorophenyl)-9-methyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a]diazepin-2-yl]-1-oxopropyl]morpholine. Grades: ≥99% by HPLC. CAS No. 105219-56-5. Molecular formula: C22H22N5O2SCl. Mole weight: 455.96. |  |
| Weck's Etchant | Weck's tint etch for Ti and alloys. Group: Etchants. |  |
| Wedelolactone | Wedelolactone. Group: Biochemicals. Alternative Names: 5,11,12-Trihydroxy-7-methoxycoumestan. Grades: Plant Grade. CAS No. 524-12-9. Pack Sizes: 20mg. Molecular Formula: C16H10O7, Molecular Weight: 314.245999999999. US Biological Life Sciences. | Worldwide |
| Wedelolactone | Wedelolactone suppresses LPS-induced caspase-11 expression by directly inhibits the IKK Complex. Wedelolactone also inhibits 5-lipoxygenase (5-Lox) with an IC50 of 2.5 μM. Wedelolactone induces caspase-dependent apoptosis in prostate cancer cells via downregulation of PKCε without inhibiting Akt. Wedelolactone can extract from Eclipta alba, and it can be used for the research of cancer. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Pentafluorobenzaldehyde. Product Category: Inhibitors. CAS No. 524-12-9. Molecular formula: C16H10O7. Mole weight: 314.25. Purity: 0.9991. Canonical SMILES: COC1=CC(=C2C(=C1)OC(=O)C3=C2OC4=CC(=C(C=C43)O)O)O. Product ID: ACM524129. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Wedelolactone | ?98% (HPLC), powder. Group: Fluorescence/luminescence spectroscopyeuropean pharmacopoeia (ph. eur.)pharmacopoeial standards. Alternative Names: Wedelolactone,1,8,9-Trihydroxy-3-methoxy-6H-benzofuro[3,2-c][1]benzopyran-6-one. | |
| Wedelolactone | Wedelolactone suppresses LPS-induced caspase-11 expression by directly inhibits the IKK Complex. Wedelolactone also inhibits 5-lipoxygenase ( 5-Lox ) with an IC 50 of 2.5 μM. Wedelolactone induces caspase-dependent apoptosis in prostate cancer cells via downregulation of PKCε without inhibiting Akt. Wedelolactone can extract from Eclipta alba, and it can be used for the research of cancer [1] [2] [3]. Uses: Scientific research. Group: Natural products. CAS No. 524-12-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0551. |  |
| Wedelolactone | Wedelolactone Inhibitor. Uses: Scientific use. Product Category: T3384. CAS No. 524-12-9. |  |
| WEHI-345 | WEHI-345, a pyrazolo-pyridine derivative, is a RIPK2 inhibitor and has been found to influence the production of inflammatory cytokine. IC50: 0.13 μM. Uses: Wehi-345 is a ripk2 inhibitor and has been found to influence the production of inflammatory cytokine. Synonyms: WEHI-345; WEHI345; WEHI 345. SCHEMBL10098386; CS-5045; HY-18937; CS 5045; HY 18937; CS5045; HY18937. Grades: 98%. CAS No. 1354825-58-3. Molecular formula: C22H23N7O. Mole weight: 401.46. | |
| WEHI-345 | WEHI-345 is a potent and selective RIPK2 kinase inhibitor with an IC 50 of 0.13 μM, which delays RIPK2 ubiquitylation and NF-κB activation on oligomerization domain (NOD) stimulation [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1354825-58-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-18937. | |
| WEHI-345 analog | WEHI-345 analog is the analog of WEHI-345. WEHI-345 is a potent and selective RIPK2 kinase inhibitor with an IC 50 of 0.13 μM, which delays RIPK2 ubiquitylation and NF-κB activation on oligomerization domain (NOD) stimulation [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1354825-62-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-100112. | |
| WEHI-345 analogue | An analogue of WEHI-345, a pyrazolo-pyridine derivative, is a protein kinase inhibitor and could be significant for studying the mechanism of cancer. Uses: An analogue of wehi-345 is a protein kinase inhibitor and could be significant for studying the mechanism of cancer. Synonyms: WEHI-345 (analog); SCHEMBL727021; CS-5569; WEHI 345 (analog); SCHEMBL 727021; CS 5569; WEHI345 (analog); SCHEMBL 727021; CS5569. Grades: 98%. CAS No. 1354825-62-9. Molecular formula: C23H25N7O. Mole weight: 415.49. | |
| WEHI-539 | WEHI-539, a selective BCL-XL inhibitor that can be function as a single-agent inducer of apoptosis while sparing normal cells, it leads to MOMP and apoptosis due to displacing bound activator BH3s or monomeric BAX and BAK from BCL-XL to induce the homo-ol. Synonyms: 4-Thiazolecarboxylic acid, 5-[3-[4-(aminomethyl)phenoxy]propyl]-2-[8-[2-(2-benzothiazolyl)hydrazinylidene]-5,6,7,8-tetrahydro-2-naphthalenyl]-; 5-[3-[4-(Aminomethyl)phenoxy]propyl]-2-[8-[2-(2-benzothiazolyl)hydrazinylidene]-5,6,7,8-tetrahydro-2-naphthalenyl]-4-thiazolecarboxylic acid; WEHI 539; WEHI539; 5-(3-(4-(aminomethyl)phenoxy)propyl)-2-(8-(2-(benzo[d]thiazol-2-yl)hydrazineylidene)-5,6,7,8-tetrahydronaphthalen-2-yl)thiazole-4-carboxylic acid. Grades: ≥95%. CAS No. 1431866-33-9. Molecular formula: C31H29N5O3S2. Mole weight: 583.73. | |
| WEHI-539 hydrochloride | WEHI-539 is a selective BCL-XL inhibitor that can function as a single-agent inducer of apoptosis while sparing normal cells. WEHI-539 provokes BAK-mediated apoptosis in BCL-XL-dependent cells. Synonyms: 4-Thiazolecarboxylic acid, 5-[3-[4-(aminomethyl)phenoxy]propyl]-2-[8-[2-(2-benzothiazolyl)hydrazinylidene]-5,6,7,8-tetrahydro-2-naphthalenyl]-, hydrochloride (1:1); 5-(3-(4-(aminomethyl)phenoxy)propyl)-2-(8-(2-(benzo[d]thiazol-2-yl)hydrazineylidene)-5,6,7,8-tetrahydronaphthalen-2-yl)thiazole-4-carboxylic acid hydrochloride; WEHI-539 HCl; 5-{3-[4-(Aminomethyl)phenoxy]propyl}-2-[8-(1,3-benzothiazol-2-ylhydrazono)-5,6,7,8-tetrahydro-2-naphthalenyl]-1,3-thiazole-4-carboxylic acid hydrochloride (1:1); WEHI539 hydrochloride; WEHI 539 hydrochloride. Grades: ≥95%. CAS No. 2070018-33-4. Molecular formula: C31H29N5O3S2.HCl. Mole weight: 620.18. | |
| WEHI-539 hydrochloride | WEHI-539 hydrochloride is a selective inhibitor of Bcl-XL with an IC50 of 1.1 nM. Uses: Scientific research. Group: Signaling pathways. CAS No. 2070018-33-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15607A. | |
| Weigert's solution | for microscopy. Group: Stains and dyes. | |
| Weinreb linker | Weinreb linker. Group: Biochemicals. Alternative Names: Fmoc-N-methoxy-3-aminopropionic acid. Grades: Highly Purified. CAS No. 247021-90-5. Pack Sizes: 1g, 2g, 5g, 10g, 25g. US Biological Life Sciences. | Worldwide |
| Weinreb Linker | Synonyms: 3- ( ( ( (9H-Fluoren-9-yl)methoxy)carbonyl) (methoxy)amino)propanoic acid; N-Fmoc-N-methoxy-3-aminopropionic acid; beta-Alanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methoxy-; N-Fmoc-N-methoxy-3-aminopropionicacid; PubChem11749; SCHEMBL1274753; N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-methoxy-Beta-alanine; Fmoc-N-methoxy-3-aminopropionic acid. Grades: > 97%. CAS No. 247021-90-5. Molecular formula: C19H19NO5. Mole weight: 341.36. | |
| Weinreb Resin | Weinreb Resin. Uses: Weinreb resin is used to prepare peptide aldehydes. it was utilized as the solid phase support in a synthesis of the macrocyclic imine scytonemide a, an inhibitor of the human 20s proteasome. Group: Unsubstituted resins. Alternative Names: N-Fmoc-N-methoxy-beta-alanine, polymer bound. Pack Sizes: 5g, 25g. | |
| Weisocyanate 98% | Weisocyanate 98%. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2-Propenamide,N-methoxy-N,2-dimethyl; Weinreb amide of 2-methyl-2-propenoic acid; di-tert-butyl 4-(3-tert-butoxy-3-oxopropyl)-4-isocyanatoheptanedioate; N-methoxy-N-methylmethacrylamide; WeisocyanateTM; N-methoxy-2,N-dimethyl-acrylamide; Di-tert-butyl 4-i. Product Category: Heterocyclic Organic Compound. CAS No. 197368-00-6. Molecular formula: C23H39NO7. Mole weight: 441.56. Purity: 0.96. IUPACName: ditert-butyl 4-(3-tert-butoxy-3-oxo-propyl)-4-isocyanato-heptaned ioat. Product ID: ACM197368006. Alfa Chemistry ISO 9001:2015 Certified. | |
| Welan gum | Cas No. 96949-22-3. | |
| Werner syndrome RecQ helicase-IN-4 | Werner syndrome RecQ helicase-IN-4 is a potent and orally active werner syndrome recQ helicase (WRN) inhibitor with an IC 50 value of 0.06 μM. Werner syndrome RecQ helicase-IN-4 shows antiproliferative activity. Werner syndrome RecQ helicase-IN-4 shows anticancer activity [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2869954-53-8. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-148741. | |
| WESTON 430 | WESTON 430. Group: Polymers. Product ID: tris[2-(2-hydroxyethoxy)ethyl] phosphite. Molecular formula: 346.31g/mol. Mole weight: C12H27O9P. C(COCCOP(OCCOCCO)OCCOCCO)O. InChI=1S / C12H27O9P / c13-1-4-16-7-10-19-22 (20-11-8-17-5-2-14) 21-12-9-18-6-3-15 / h13-15H, 1-12H2. ZBSCMUKWGDDOQK-UHFFFAOYSA-N. | |
| Weston EHDP | Weston EHDP. Group: Polymers. | |
| Weston PDDP | Weston PDDP. Group: Polymers. | |
| Weston TDP | Weston TDP. Group: Polymers. | |
| WESTREZ 5101P | WESTREZ 5101P. Group: Polymers. | |
| WF-10129 | WF-10129 is an angiotensin converting enzyme (ACE) inhibitor produced by Doratomyces putredinis, with IC50 of 1.4 X 10(-8) M. Synonyms: WF 10129. CAS No. 109075-64-1. Molecular formula: C20H28N2O8. Mole weight: 424.4. | |
| WF11605 | WF11605 is an antagonist of leukotriene B4 (LTB4) isolated from the fungal strain F11605. It inhibited LTB4-induced chemotaxis of rabbit polymorphonuclear leukocytes (PMNLs) with an IC50 value of 1.7 x 10(-7) M and blocked 3H-LTB4 binding to PMNL membranes at 5.6 x 10(-6) M (IC50). It also inhibited LTB4-induced degranulation of rabbit PMNLs at 3.0 x 10(-6) M (IC50). Synonyms: WF 11605; WF-11605. CAS No. 127475-47-2. Molecular formula: C38H60O11. Mole weight: 692.9. | |
| WF11899A | WF11899A is a lipopeptide antibiotic isolated from the culture broth of Coleophoma empetri F-11899. It shows antifungal activity against Candida spp. Synonyms: WF-11899A. Molecular formula: C51H82N8O21S. Mole weight: 1175.3. | |
| WF11899B | WF11899B is a lipopeptide antibiotic isolated from the culture broth of Coleophoma empetri F-11899. It shows antifungal activity against Candida spp. Synonyms: WF-11899B. Molecular formula: C51H82N8O20S. Mole weight: 1159.3. | |
| WF11899C | WF11899C is a lipopeptide antibiotic isolated from the culture broth of Coleophoma empetri F-11899. It shows antifungal activity against Candida spp. Synonyms: WF-11899C. Molecular formula: C51H82N8O19S. Mole weight: 1143.3. | |
| WF-1360B | WF-1360B is one component of Rhizoxin complex produced by Rhizopus sp. No. F-1360. It was highly active against leukemia L1210 and melanoma B16. Synonyms: Antibiotic WF-1360B. Molecular formula: C34H45NO8. Mole weight: 595.72. | |
| WF-1360C | WF-1360C is one component of Rhizoxin complex produced by Rhizopus sp. No. F-1360. It was highly active against leukemia L1210 and melanoma B16. Synonyms: Antibiotic WF-1360C. Molecular formula: C34H45NO9. Mole weight: 611.72. | |
| WF-1360E | WF-1360E is one component of Rhizoxin complex produced by Rhizopus sp. No. F-1360. It was highly active against leukemia L1210 and melanoma B16. Synonyms: Antibiotic WF-1360E. Molecular formula: C37H53NO9. Mole weight: 655.82. | |
| WF-1360F | WF-1360F is one component of Rhizoxin complex produced by Rhizopus sp. No. F-1360. It was highly active against leukemia L1210 and melanoma B16. Synonyms: Antibiotic WF-1360F. Molecular formula: C35H47NO8. Mole weight: 609.75. | |
| WF14861 | WF14861 is a cathepsins B and L inhibitor obtained from the culture mycelium of a fungus strain Colletotrichum sp. No. 14861. Synonyms: WF 14861; WF-14861. Molecular formula: C20H30N4O6. Mole weight: 422.5. | |
| WF14865A | WF14865A is a cathepsins B and L inhibitor with IC50 of 8.4 X 10(-9) and 6.6 X 10(-8) mol/L, respectively. It is produced by Aphanoascus fulvescens. Synonyms: WF-14865A. Molecular formula: C16H25N5O5. Mole weight: 367.4. | |
| WF14865B | WF14865B is a cathepsins B and L inhibitor with IC50 of 1.3 X 10(-8) and 7.2 X 10(-8) mol/L, respectively. It is produced by Aphanoascus fulvescens. Synonyms: WF-14865B. Molecular formula: C17H27N5O5. Mole weight: 381.43. | |
| WF-2421 | WF-2421 is an aldose reductase inhibitor produced by Humicola grisea. Synonyms: WF 2421. CAS No. 128429-19-6. Molecular formula: C19H20N2O8. Mole weight: 404.4. | |
| WF-3161 | WF-3161 is an antitumor antibiotic produced by a strain of fungus, Petriella guttulata. It inhibited the growth of Trichophyton asteroides. Synonyms: Antibiotic WF 3161; WF 3161; Antibiotic FR 900261; WF-3161. CAS No. 86402-37-1. Molecular formula: C31H44N4O6. Mole weight: 568.7. | |
| WF-3405 | WF-3405 is an antitumor antibiotic isolated from the culture of Amauroascus aureus F-3405. It inhibits various murine tumors including leukemia P388, leukemia L1210 and Lewis lung carcinoma. Synonyms: Antibiotic WF 3405; WF 3405. CAS No. 108354-43-4. Molecular formula: C9H16O7. Mole weight: 236.22. | |
| WF-3681 | WF-3681 is an aldose reductase inhibitor produced by Chaetomella raphigera Swift No. 3681. Synonyms: WF 3681. CAS No. 105364-56-5. Molecular formula: C13H12O5. Mole weight: 248.23. | |
| WF-5239 | WF-5239 is produced by a fungal strain identified as Aspergillus fumigatus Fresenius. It acts as a potent platelet aggregation inhibitor. Synonyms: WF 5239. CAS No. 91224-36-1. Molecular formula: C9H9NO2. Mole weight: 163.17. | |
| WH-15 | WH-15 is a fluorogenic PLC reporter with K m value of 49; 30, 86.1 μM for PLC-γ1, PLC-δ1, PLC-β2, respectively. WH-15 can be cleaved in a cascade reaction to generate fluorescent 6-aminoquinoline. WH-15 can be used to respond to imaging PLC activity in live cells [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1264748-47-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-135799. | |
| WH-4-023 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| WH-4-023 | WH-4-023. Group: Biochemicals. Grades: Highly Purified. CAS No. 837422-57-8. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| WH-4-023 | WH-4-023 is a potent and selective dual Lck/Src inhibitor with IC50 of 2 nM/6 nM for Lck and Src kinase respectively; little inhibition on p38? and KDR. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Dual LCK/SRC inhibitor. CAS No. 837422-57-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-12299. | |
| WH-4-023 | WH-4-023 is a potent and selective dual Lck/Src inhibitor with IC50 values of 2 nM and 6 nM for Lck and Src kinase respectively. In combination with PD 0325901, CHIR99021 and SB-590885, WH-4-023 was found to support self-renewal of naive human embryonic stem cells (hESCs). Synonyms: KIN001-112; KIN112; 2,6-dimethylphenyl (2,4-dimethoxyphenyl)(2-((4-(4-methylpiperazin-1-yl)phenyl)amino)pyrimidin-4-yl)carbamate. Grades: >98%. CAS No. 837422-57-8. Molecular formula: C32H36N6O4. Mole weight: 568.67. | |
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