American Chemical Suppliers

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Product
ST638 ?98% (HPLC), solid. Group: Fluorescence/luminescence spectroscopy. Alfa Chemistry Analytical Products 3
ST91 ST91 is a α 2 -adrenoceptor (α 2 AR) agonist. ST91 activates both α 2A AR and non-α 2A AR subtypes to produce spinal antinociception [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 4749-61-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-103203. MedChemExpress MCE
ST 91 ST 91. Group: Biochemicals. Grades: Purified. CAS No. 4749-61-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. USBiological 5
Worldwide
STA-21 ?95% (HPLC). Group: Fluorescence/luminescence spectroscopy. Alfa Chemistry Analytical Products
STA-4783 STA-4783 Inhibitor. Uses: Scientific use. Product Category: T6170. CAS No. 488832-69-5. TARGETMOL CHEMICALS
Stabilized Gold Nanoparticles Stabilized Gold Nanoparticles. Uses: Conjugate development, immunostaining, lateral flow assays, biological sensor development (e.g. lspr-based assays), electron microscopy, dark field microscopy, surface enhanced raman spectroscopy (sers). Group: other s. Alfa Chemistry Materials 3
Stabilizer 9000 (technical grade) Stabilizer 9000 (technical grade). Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2,4-Diisocyanato-1,3,5-tris(1-methyl)-benzene homopolymer. Product Category: Promotional Products. CAS No. 29963-44-8. Purity: Tech. Product ID: ACM29963448-1. Alfa Chemistry — ISO 9001:2015 Certified. Alfa Chemistry.
Stachartin A Stachartin A is produced in the cultures of the tin mine tailings-associated fungus Stachybotrys chartarum. Synonyms: Stachybotrysin; 3-Buten-2-one, 4-[(1'R,2'R,4'aS,6'R,8'aS)-3',4',4'a,5',6',7',8',8'a-octahydro-4,6'-dihydroxy-6-(hydroxymethyl)-2',5',5',8'a-tetramethylspiro[benzofuran-2(3H), 1'(2'H)-naphthalen]-7-yl]-, (3E)-. Grade: 98.0%. CAS No. 1978388-54-3. Molecular formula: C26H36O5. Mole weight: 428.56. BOC Sciences 8
Stachartin B Stachartin B is produced in the cultures of the tin mine tailings-associated fungus Stachybotrys chartarum. Synonyms: Stachybotrylactone B; Spiro[benzo[2,1-b:3,4-c']difuran-2(8H),1'(2'H)-naphthalen]-8-one, 3,3',4',4'a,5',6,6',7',8',8'a-decahydro-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-, (1'R,2'R,4'aS,6'R,8'aS)-. Grade: 97.5%. CAS No. 1978388-55-4. Molecular formula: C23H30O5. Mole weight: 386.48. BOC Sciences 12
Stachartin C Stachartin C is produced in the cultures of the tin mine tailings-associated fungus Stachybotrys chartarum. Synonyms: Stachybotrylactone C. Grade: 98.0%. CAS No. 1978388-56-5. Molecular formula: C29H41NO6. Mole weight: 499.64. BOC Sciences 8
Stachartin D Stachartin D is produced in the cultures of the tin mine tailings-associated fungus Stachybotrys chartarum. Synonyms: Stachybotrylactone D. Grade: 97.0%. CAS No. 1978388-57-6. Molecular formula: C30H43NO6. Mole weight: 513.67. BOC Sciences 12
Stachartin E Stachartin E is produced in the cultures of the tin mine tailings-associated fungus Stachybotrys chartarum. Synonyms: Stachybotrylactone E. Grade: 98.0%. CAS No. 1978388-58-7. Molecular formula: C33H41NO6. Mole weight: 547.68. BOC Sciences 8
Stachybocin A It is a receptor antagonist produced by the strain of Stachybotrys sp. M6222. It inhibits the binding of I-ET-1 to rat ETA receptors with IC50 of 2.3 X 10-5 (mol/L). It also inhibits the binding of I-ET-1 to human ETA receptors and human ETB receptors with IC50 (mol/L) of 1.3 X 10-5 and 7.9 X 10-6, respectively. Synonyms: Spirodihydrobenzofuranlactam ?; Spiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalene]-7(3H)-hexanoic acid, a-[(1'R,2'R,4'aS,6'R,8'aS)-3',4',4'a,5',6,6',7',8,8',8'a-decahydro-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-6-oxospiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalen]-7(3H)-yl]-3',4',4'a,5',6,6',7',8,8',8'a-decahydro-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-6-oxo-, (aS,1'R,2'R,4'aS,6'R,8'aS)-; Spiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalene]-7(3H)-hexanoic acid, a-(3',4',4'a,5',6,6',7',8,8',8'a-decahydro-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-6-oxospiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalen]-7(3H)-yl)-3',4',4'a,5',6,6',7',8,8',8'a-decahydro-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-6-oxo-, [1'R-[1'a[S*(1'R*,2'R*,4'aS*,6'R*,8'S*)],2'a,4'aa,6'a,8'ab]]-; AM 6222A. CAS No. 158827-60-2. Molecular formula: C52H70N2O10. Mole weight: 883.12. BOC Sciences 12
Stachybocin B It is a receptor antagonist produced by the strain of Stachybotrys sp. M6222. It inhibits the binding of I-ET-1 to rat ETA receptors with IC50 of 2.8 X 10-5 (mol/L). It also inhibits the binding of I-ET-1 to human ETA receptors and human ETB receptors with IC50 (mol/L) of 1.2 X 10-5 and 9.5 X 10-6, respectively. Synonyms: Spiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalene]-7(3H)-hexanoic acid, a-[(1'R,2'R,4'aS,6'S,7'R,8'aS)-3',4',4'a,5',6,6',7',8,8',8'a-decahydro-4,6',7'-trihydroxy-2',5',5',8'a-tetramethyl-6-oxospiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalen]-7(3H)-yl]-3',4',4'a,5',6,6',7',8,8',8'a-decahydro-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-6-oxo-, (aS,1'R,2'R,4'aS,6'R,8'aS)-; Spiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalene]-7(3H)-hexanoic acid, a-(3',4',4'a,5',6,6',7',8,8',8'a-decahydro-4,6',7'-trihydroxy-2',5',5',8'a-tetramethyl-6-oxospiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalen]-7(3H)-yl)-3',4',4'a,5',6,6',7',8,8',8'a-decahydro-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-6-oxo-, [1'R-[1'a[S*(1'R*,2'R*,4'aS*,6'R*,8'S*)],2'a,4'aa,6'a,7'a,8'ab]]-; AM 6222B. CAS No. 158827-61-3. Molecular formula: C52H70N2O11. Mole weight: 899.12. BOC Sciences 12
Stachybocin C It is a receptor antagonist produced by the strain of Stachybotrys sp. M6222. It inhibits the binding of I-ET-1 to rat ETA receptors with IC50 of 2.9 X 10-5 (mol/L). It also inhibits the binding of I-ET-1 to human ETA receptors and human ETB receptors with IC50 (mol/L) of 1.5 X 10-5 and 9.4 X 10-6, respectively. Synonyms: Spiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalene]-7(3H)-hexanoic acid, a-[(1'R,2'R,4'aS,6'R,8'aS)-3',4',4'a,5',6,6',7',8,8',8'a-decahydro-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-6-oxospiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalen]-7(3H)-yl]-3',4',4'a,5',6,6',7',8,8',8'a-decahydro-4,6',7'-trihydroxy-2',5',5',8'a-tetramethyl-6-oxo-, (aS,1'R,2'R,4'aS,6'S,7'R,8'aS)-; Spiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalene]-7(3H)-hexanoic acid, a-(3',4',4'a,5',6,6',7',8,8',8'a-decahydro-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-6-oxospiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalen]-7(3H)-yl)-3',4',4'a,5',6,6',7',8,8',8'a-decahydro-4,6',7'-trihydroxy-2',5',5',8'a-tetramethyl-6-oxo-, [1'R-[1'a[S*(1'R*,2'R*,4'aS*,6'R*,8'aS*)],2'a,4'aa,6'a,7'a,8'ab]]-; AM 6222C. CAS No. 158827-62-4. Molecular formula: C52H70N2O11. Mole weight: 899.12. BOC Sciences 12
Stachybotramide Stachybotramide is produced by the mycelia and culture broth of Stachybotrys sp. Stachybotramide can stimulate the plasma cholesteryl ester transfer protein (CETP)-mediated transfer of cholesteryl esters (CE) from high density lipoprotein (HDL) to very low density lipoprotein (VLDL) and low density lipoprotein (LDL). Synonyms: Spirodihydrobenzofuranlactam II; Spiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalen]-6(3H)-one, 3',4',4'a,5',6',7,7',8,8',8'a-decahydro-4,6'-dihydroxy-7-(2-hydroxyethyl)-2',5',5',8'a-tetramethyl-, (1'R,2'R,4'aS,6'R,8'aS)-; (1'R,2'R,4'aS,6'R,8'aS)-3',4',4'a,5',6',7,7',8,8',8'a-Decahydro-4,6'-dihydroxy-7-(2-hydroxyethyl)-2',5',5',8'a-tetramethylspiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalen]-6(3H)-one; Stachybotrin; Spiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalen]-6(3H)-one, 3',4',4'a,5',6',7,7',8,8',8'a-decahydro-4,6'-dihydroxy-7-(2-hydroxyethyl)-2',5',5',8'a-tetramethyl-, [1'R-(1'α,2'α,4'aα,6'α,8'aβ)]-. Grade: 97.5%. CAS No. 149598-71-0. Molecular formula: C25H35NO5. Mole weight: 429.55. BOC Sciences 12
Stachybotrin A It is produced by the strain of Stachyborrys sp. It has antimicrobial and antifungal activity. CAS No. 144373-26-2. Molecular formula: C23H31NO5. Mole weight: 401.49. BOC Sciences 12
Stachybotrin B It is produced by the strain of Stachyborrys sp. It has antimicrobial and antifungal activity. Synonyms: (+)-Stachybotrin B. CAS No. 144385-02-4. Molecular formula: C23H31NO4. Mole weight: 385.50. BOC Sciences 12
Stachybotrin C It is a neuritogenic agent produced by the strain of Stachyborrys parvispora F4708. It promotes the enlargement of the neural sinus of P12 cells, and the effect of Stachybotrin C is obvious, but the effect of Parvisporin is weak. Synonyms: Pyrano[2,3-e]isoindol-7(2H)-one, 2-[(3E)-4,8-dimethyl-3,7-nonadien-1-yl]-3,4,8,9-tetrahydro-3,5-dihydroxy-8-[2-(4-hydroxyphenyl)ethyl]-2-methyl-, (2R,3R)-rel-; Pyrano[2,3-e]isoindol-7(2H)-one, 2-(4,8-dimethyl-3,7-nonadienyl)-3,4,8,9-tetrahydro-3,5-dihydroxy-8-[2-(4-hydroxyphenyl)ethyl]-2-methyl-, [2a(E),3a]-; Antibiotic NG 245. CAS No. 150351-23-8. Molecular formula: C31H39NO5. Mole weight: 505.64. BOC Sciences 12
Stachybotrolide Stachybotrolide is produced by Stachybotrys alternans. Synonyms: Stachybotrylactone; (2R,2'R,4a'S,6'R,8a'S)-4,6'-dihydroxy-2',5',5',8a'-tetramethyl-3',4',4a',5',6',7',8',8a'-octahydro-2'H,3H-spiro[benzo[2,1-b:3,4-c']difuran-2,1'-naphthalen]-6(8H)-one; Spiro[benzo[2,1-b:3,4-c']difuran-2(3H),1'(2'H)-naphthalen]-6(8H)-one, 3',4',4'a,5',6',7',8',8'a-octahydro-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-, [1'R-(1'α,2'α,4'aα,6'α,8'aβ)]-; Spiro[benzo[2,1-b:3,4-c']difuran-2(3H),1'(2'H)-naphthalen]-6(8H)-one, 3',4',4'a,5',6',7',8',8'a-octahydro-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-, (1'R,2'R,4'aS,6'R,8'aS)-. Grade: 97.5%. CAS No. 149691-31-6. Molecular formula: C23H30O5. Mole weight: 386.48. BOC Sciences 12
Stachybotrylactam An unusual spirodihydrobenzofuranlactam mycotoxin isolated from Stachybotrys sp. It shows immunosuppressant and weak HIV protease activity and shows diverse activity including antiviral, endothelin and pancreatic cholesterase inhibition. Synonyms: Stachybotrylactam; 163391-76-2; 3,4'-dihydroxy-4,4,7,8a-tetramethylspiro[2,3,4a,5,6,7-hexahydro-1H-naphthalene-8,2'-7,8-dihydro-3H-furo[2,3-e]isoindole]-6'-one; Spiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalen]-6(3H)-one, 3',4',4'a,5',6',7,7',8,8',8'a-decahydro-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-, (1'R,2'R,4'aS,6'R,8'aS)-; CID 45934402; Compound NP-020819; DTXSID70672955; CHEBI:201797; AKOS040737949; J-010041; (3R,4aS,7R,8R,8aS)-3,4'-dihydroxy-4,4,7,8a-tetramethylspiro[2,3,4a,5,6,7-hexahydro-1H-naphthalene-8,2'-7,8-dihydro-3H-uro[2,3-e]isoindole]-6'-one; 4,6'-DIHYDROXY-2',5',5',8'A-TETRAMETHYL-3',4',4'A,6',7,7',8,8'-OCTAHYDRO-2'H,3H-SPIRO[FURO[2,3-E]ISOINDOLE-2,1'-NAPHTHALEN]-6-ONE. Grade: >95% by HPLC. CAS No. 163391-76-2. Molecular formula: C23H31NO4. Mole weight: 385.50. BOC Sciences 12
Stachybotrylactam (2-deoxy Antibiotic F1839A) Isolated from a Stachybotrys sp., this unusual spirodi hydrobenzofuranlactam mycotoxin shows immuno-suppressant and weak HIV protease activity. Members of this structural class show diverse activity including antiviral, endothelin and pancreatic cholesterase inhibition. Group: Biochemicals. Alternative Names: 2-deoxy Antibiotic F1839A. Grades: Highly Purified. CAS No. 163391-76-2. Pack Sizes: 500ug. US Biological Life Sciences. USBiological 1
Worldwide
Stachydrine Stachydrine. Group: Biochemicals. Grades: Plant Grade. CAS No. 471-87-4. Pack Sizes: 20mg. Molecular Formula: C7H13NO2, Molecular Weight: 143.18. US Biological Life Sciences. USBiological 9
Worldwide
Stachydrine Stachydrine is a major constituent of Chinese herb leonurus heterophyllus sweet used to promote blood circulation and dispel blood stasis. Stachydrine can inhibit the NF-κB signal pathway. Uses: Scientific research. Group: Natural products. CAS No. 471-87-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-N0298. MedChemExpress MCE
Stachydrine hydrochloride Stachydrine hydrochloride is the major active constituent of Leonurus artemisia , which is a potential therapy for cardiovascular diseases [2]. Stachydrine can inhibit the NF-κB signal pathway. Anti-hypertrophic activities [1]. Uses: Scientific research. Group: Natural products. CAS No. 4136-37-2. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-N0738. MedChemExpress MCE
Stachydrine hydrochloride Stachydrine hydrochloride is extracted from the flower of Chrysanthemum parthenium. It promoted the protein expression of IL-12 and IL-6, as well as the mRNA expression of T-bet and RORγt, while inhibiting the mRNA expression of GATA-3 and Foxp3. Synonyms: Pyrrolidinium, 2-carboxy-1,1-dimethyl-, chloride (1:1), (2S)-; Pyrrolidinium, 2-carboxy-1,1-dimethyl-, chloride, (2S)-; Pyrrolidinium, 2-carboxy-1,1-dimethyl-, chloride, (S)-; Stachydrine, chloride; Cadabine hydrochloride; (S)-2-Carboxy-1,1-dimethylpyrrolidinium chloride; (S)-2-Carboxy-1,1-dimethylpyrrolidin-1-ium chloride. Grade: >98%. CAS No. 4136-37-2. Molecular formula: C7H14ClNO2. Mole weight: 179.64. BOC Sciences 9
Stachydrine Hydrochloride Stachydrine hydrochloride is extracted from the flower of Chrysanthemum parthenium. It promoted the protein expression of IL-12 and IL-6, as well as the mRNA expression of T-bet and RORγt, while inhibiting the mRNA expression of GATA-3 and Foxp3. Group: Biochemicals. Alternative Names: Turicine HCl; (S)-2-Carboxy-1,1-dimethylpyrrolidinium chloride; 2-Carboxy-1,1-dimethylpyrrolidinium chloride. Grades: Highly Purified. CAS No. 4136-37-2. Pack Sizes: 50mg. US Biological Life Sciences. USBiological 8
Worldwide
Stachyose Stachyose, a kind of oligosaccharides, act as a hypoglycemic agent [1]. Uses: Scientific research. Group: Natural products. CAS No. 470-55-3. Pack Sizes: 5 mg; 10 mg. Product ID: HY-N7910. MedChemExpress MCE
Stachyose hydrate Stachyose hydrate is an orally active prebiotic that enhances the growth and activity of beneficial bacteria. Stachyose hydrate has hypoglycemic effects and can improve inflammation by regulating gut microbiota. In addition, Stachyose hydrate can induce plant cell apoptosis ( Apoptosis ). Stachyose hydrate can be used in research on inflammation, gastrointestinal diseases, and agriculture [1] [2] [3]. Uses: Scientific research. Group: Natural products. CAS No. 54261-98-2. Pack Sizes: 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-N0299. MedChemExpress MCE
Stafia-1 Stafia-1 is a potent STAT5a inhibitor ( K i =10.9 μM, IC 50 =22.2 μM). Stafia-1 displays high selectivity over STAT5b and other STAT family members [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2582757-90-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-136546. MedChemExpress MCE
Stafib-1 Stafib-1 is the first selective inhibitor of the STAT5b SH2 domain, with a Ki of 44 nM and an IC50 of 154 nM[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1688703-26-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-112647. MedChemExpress MCE
Stafib-2 Stafib-2 is a potent and selctive inhibitor of the transcription factor STAT5b , with an IC 50 of 82 nM and 1.7 μM for STAT5b and STAT5a , respectively. Stafib-2 exhibits poor cell permeability [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2097938-74-2. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-112648. MedChemExpress MCE
S Tag Peptide S Tag Peptide, a 15 amino acid peptide derived from RNase A, is an oligopeptide used for improving protein solubility. Synonyms: Lys-Glu-Thr-Ala-Ala-Ala-Lys-Phe-Glu-Arg-Gln-His-Met-Asp-Ser; L-lysyl-L-alpha-glutamyl-(3xi)-L-threonyl-L-alanyl-L-alanyl-L-alanyl-L-lysyl-L-phenylalanyl-L-alpha-glutamyl-L-arginyl-L-glutaminyl-L-histidyl-L-methionyl-L-alpha-aspartyl-L-serine; S Tag. Grade: ≥95%. Molecular formula: C73H117N23O25S. Mole weight: 1748.91. BOC Sciences
Stainless Steel disc, 102mm (4.0in) dia x 12.7mm (0.5in) thick, Type 304 Stainless Steel disc, 102mm (4.0in) dia x 12.7mm (0.5in) thick, Type 304. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel disc, 152mm (6.0in) dia x 12.7mm (0.5in) thick, Type 304 Stainless Steel disc, 152mm (6.0in) dia x 12.7mm (0.5in) thick, Type 304. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel disc, 76mm (3.0in) dia x 12.7mm (0.5in) thick, Type 304 Stainless Steel disc, 76mm (3.0in) dia x 12.7mm (0.5in) thick, Type 304. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel flake, -150 mesh, 1.2 micron thick, Type 316-L Stainless Steel flake, -150 mesh, 1.2 micron thick, Type 316-L. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel flake, -325 mesh, 0.4-1.2 micron thick, Type 316-L Stainless Steel flake, -325 mesh, 0.4-1.2 micron thick, Type 316-L. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel foil, 0.025mm (0.001in) thick, Type 304 Stainless Steel foil, 0.025mm (0.001in) thick, Type 304. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel foil, 0.05mm (0.002in) thick, Type 304 Stainless Steel foil, 0.05mm (0.002in) thick, Type 304. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel foil, 0.1mm (0.004in) thick, Type 304 Stainless Steel foil, 0.1mm (0.004in) thick, Type 304. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel foil, 0.25mm (0.01in) thick, Type 304 Stainless Steel foil, 0.25mm (0.01in) thick, Type 304. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel foil, 0.2mm (0.008in) thick, Type 304 Stainless Steel foil, 0.2mm (0.008in) thick, Type 304. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel foil, 0.5mm (0.02in) thick, Type 304 Stainless Steel foil, 0.5mm (0.02in) thick, Type 304. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel gauze, 100 mesh woven from 0.025mm (0.001in) dia wire, Type 304 Stainless Steel gauze, 100 mesh woven from 0.025mm (0.001in) dia wire, Type 304. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel gauze, 100 mesh woven from 0.11mm (0.0045in) dia wire, Type 316 Stainless Steel gauze, 100 mesh woven from 0.11mm (0.0045in) dia wire, Type 316. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel gauze, 150 mesh woven from 0.066mm (0.0026in) dia wire, Type 304 Stainless Steel gauze, 150 mesh woven from 0.066mm (0.0026in) dia wire, Type 304. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel gauze, 200 mesh woven from 0.05mm (0.002in) dia wire, Type 304 Stainless Steel gauze, 200 mesh woven from 0.05mm (0.002in) dia wire, Type 304. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel gauze, 200 mesh woven from 0.05mm (0.002in) dia wire, Type 316 Stainless Steel gauze, 200 mesh woven from 0.05mm (0.002in) dia wire, Type 316. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel gauze, 20 mesh woven from 0.102mm (0.004in) dia wire, Type 316 Stainless Steel gauze, 20 mesh woven from 0.102mm (0.004in) dia wire, Type 316. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel gauze, 20 mesh woven from 0.382mm (0.015in) dia wire, Type 304 Stainless Steel gauze, 20 mesh woven from 0.382mm (0.015in) dia wire, Type 304. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel gauze, 325 mesh woven from 0.036mm (0.0014in) dia wire, Type 316 Stainless Steel gauze, 325 mesh woven from 0.036mm (0.0014in) dia wire, Type 316. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel gauze, 400 mesh woven from 0.028mm (0.0011in) dia wire, twilled weave, Type 304 Stainless Steel gauze, 400 mesh woven from 0.028mm (0.0011in) dia wire, twilled weave, Type 304. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel gauze, 40 mesh woven from 0.25mm (0.01in) dia wire, Type 304 Stainless Steel gauze, 40 mesh woven from 0.25mm (0.01in) dia wire, Type 304. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel gauze, 500 mesh woven from 0.02mm (0.0009in) dia wire, Type 304 Stainless Steel gauze, 500 mesh woven from 0.02mm (0.0009in) dia wire, Type 304. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel gauze, 80 mesh woven from 0.127mm (0.005in) dia wire, Type 304 Stainless Steel gauze, 80 mesh woven from 0.127mm (0.005in) dia wire, Type 304. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel gauze, 80 mesh woven from 0.14mm (0.0055in) dia wire, Type 316 Stainless Steel gauze, 80 mesh woven from 0.14mm (0.0055in) dia wire, Type 316. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel Nanoparticles Stainless Steel Nanoparticles. Group: Metal nano dispersion. Alternative Names: Martensitic steel. CAS No. 65997-19-5. Mole weight: Fe/Cr/Ni. 99.9%. Alfa Chemistry Materials 3
Stainless Steel Nanoparticles/Nanopowder (316L, 40-60 nm) Stainless Steel Nanoparticles/Nanopowder (316L, 40-60 nm). Uses: Probing, recording media, ferro fluids and pastes, medical applications, environmental, catalysts, electromagnetic-wave absorption. Group: Elements nanoparticles. Alfa Chemistry Materials 3
Stainless Steel Nanoparticles/Nanopowder (316L, 60-80 nm) Stainless Steel Nanoparticles/Nanopowder (316L, 60-80 nm). Uses: Probing, recording media, ferro fluids and pastes, medical applications, environmental, catalysts, electromagnetic-wave absorption. Group: Elements nanoparticles. Alfa Chemistry Materials 3
Stainless Steel powder, -100 mesh, annealed, Type 410-L Stainless Steel powder, -100 mesh, annealed, Type 410-L. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel powder, -100 mesh, Type 304-L Stainless Steel powder, -100 mesh, Type 304-L. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel powder, -100 mesh, Type 316-L Stainless Steel powder, -100 mesh, Type 316-L. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel powder, -10+20 mesh, Type 316-L Stainless Steel powder, -10+20 mesh, Type 316-L. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel powder, -140 mesh, Type 303-L Stainless Steel powder, -140 mesh, Type 303-L. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel powder, -16+25 mesh, Type 316-L Stainless Steel powder, -16+25 mesh, Type 316-L. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel powder, 200 mesh Stainless Steel powder, 200 mesh. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel powder, -20+35 mesh, Type 316-L Stainless Steel powder, -20+35 mesh, Type 316-L. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel powder, -325 mesh, Type 316-L Stainless Steel powder, -325 mesh, Type 316-L. Group: Alloys. Alfa Chemistry Materials 6
Stainless Steel powder, -325 mesh, Type 430-L Stainless Steel powder, -325 mesh, Type 430-L. Group: Alloys. Alfa Chemistry Materials 6

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