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| Product | Description | |
|---|---|---|
| 3,3-Diphenylpropionic Acid | 3,3-Diphenylpropionic Acid is used in the preparation of steroid 5α-reductase inhibiting acylpiperidines. It can also be used in the preparation of calpain-inhibitory piptidyl α-ketoacids and esters. Group: Biochemicals. Alternative Names: β-Phenylbenzenepropanoic Acid; Diphenylpropionic Acid; NSC 631492; NSC 6797; β-Phenylbenzenepropanoic Acid. Grades: Highly Purified. CAS No. 606-83-7. Pack Sizes: 25g, 50g, 100g, 250g, 500g. Molecular Formula: C??H??O?, Molecular Weight: 226.27. US Biological Life Sciences. |  Worldwide |
| 3,5-Dinitrosalicylic acid | 3,5-Dinitrosalicylic acid the derivative of salicylic acid. 3,5-Dinitrosalicylic acid is used in the α-amylase assay, carbohydrase assay, and for the colorimetric determination of reducing substances [1]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 609-99-4. Pack Sizes: 25 g; 100 g. Product ID: HY-W009694. |  |
| 3,5-Dinitrosalicylic acid 99+% (HPLC) | 3,5-Dinitrosalicylic acid (DNS) is used in colorimetric determination of reducing sugars and to analyze glycosidase (glycoside hydrolase) activity by quantitation of enzymatically released reducing sugar. The dinitrosalicylic acid method has been compared to the Nelson-Somogi colorimetric method. 3,5-Dinitrosalicylic acid (DNS) has been used to stop the reaction in in vitro α-amylase inhibition study. It has also been used for the quantitation of enzymatically released reducing sugars. Group: Biochemicals. Alternative Names: 2-Hydroxy-3,5-dinitro-benzoic Acid; 2-Hydroxy-3,5-dinitrobenzoic Acid; 3,5-Dinitro-2-hydroxybenzoic Acid; NSC 181. Grades: Highly Purified. CAS No. 609-99-4. Pack Sizes: 25g, 100g, 250g, 1Kg. Molecular Formula: C7H4N2O7. US Biological Life Sciences. | Worldwide |
| 4-(1',5'-Dihydro-1'-methyl-2'H-[5,6]fullereno-C60-Ih-[1,9-c]pyrrol-2'-yl)benzoic acid | 4-(1',5'-Dihydro-1'-methyl-2'H-[5,6]fullereno-C60-Ih-[1,9-c]pyrrol-2'-yl)benzoic acid (C60-SAM) is a fullerene based self-assembled monolayer that can be used to functionalize the oxide surface for the formation electron selective layer (ECL). It can act as a good electron donor with a high electron affinity. It enhances the overall efficiency of perovskite solar cells (PSCs) by reducing the hysteresis. Uses: Fullerene-based self-assembled monolayers for use in organic electronic devices such as inverted polymer solar cells and perovskite-polymer hybrid solar cells. Group: Carbon nano materials organic solar cell (opv) materials. Alternative Names: C60-SAM. CAS No. 631918-72-4. Pack Sizes: 100 mg. Molecular formula: 897.84 g/mol. Mole weight: C70H11NO2. CN1CC23C4=C5C6=C7C4=C8C9=C4C% 10=C% 11C% 12=C% 13C% 10=C% 10C9=C7C7=C% 10C9=C% 10C% 14=C% 15C% 16=C% 17C (=C% 12C% 12=C% 17C% 17=C% 18C% 16=C% 16C% 15=C% 15C% 10=C7C6=C% 15C6=C% 16C7=C% 18C% 10=C (C2 (C1C1=CC=C (C=C1) C (=O) O) C7=C65) C1=C2C (=C4C8=C31) C% 11=C% 12C2=C% 17% 10) C% 14=C% 139. InChI= 1S / C70H11NO2 / c1-71-6-69-63-56-49-37-29-20-11-9-10- 12-15 (11) 24-31 (29) 39-40-32 (24) 30-21 (12) 23-19-14 (10) 17-16-13 (9) 18-22 (20) 35 (37) 43-41-27 (18) 25 (16) 33-34-26 (17) 28 (19) 42-44-36 (23) 38 (30) 50-52 (40) 61 (60 (63) 51 (39) 49) 65-58 (50) 55 (44) 59-48 (42) 46 (34) 53-45 (33) 47 (41) 57 ( |  |
| 6-Aminocaproic acid | 6-Aminocaproic acid (EACA), a monoamino carboxylic acid, is a potent and orally active inhibitor of plasmin and plasminogen. 6-Aminocaproic acid is a potent antifibrinolytic agent. 6-Aminocaproic acid prevents clot lysis through the competitive binding of lysine residues on plasminogen, inhibiting plasmin formation and reducing fibrinolysis. 6-Aminocaproic acid can be used for the research of bleeding disorders [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: EACA; Epsilon-Amino-n-caproic Acid; 6-Aminohexanoic acid. CAS No. 60-32-2. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-B0236. | |
| (6R,7R) | Heterocyclic Organic Compound. Alternative Names: [6R-[3(Z),6α,7β]]-3-[2-(4-Methyl-5-thiazolyl)ethenyl]-8-oxo-7-[(phenylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid Diphenylmethyl Ester; (6R,7R)-7-Phenylacetamido-3-[(1Z)-2-(4-methyl-5-thiazolyl)ethenyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid Diphenyl Methyl Ester. CAS No. 112953-21-6. Molecular formula: C34H29N3O4S2. Mole weight: 607.74. Appearance: Red Solid. Purity: 0.96. IUPACName: benzhydryl (6R,7R)-3-[(Z)-2-(4-methyl-1,3-thiazol-5-yl)ethenyl]-8-oxo-7-[(2-phenylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate. Canonical SMILES: CC1=C (SC=N1)C=CC2=C (N3C (C (C3=O)NC (=O)CC4=CC=CC=C4)SC2)C (=O)OC (C5=CC=CC=C5)C6=CC=CC=C6. Catalog: ACM112953216. |  |
| Acetamide | Acetamide is the simplest amide derived from acetic acid. It finds some use as a plasticizer and as an industrial solvent. Acetamide (2.88 g/kg/d) can reduce central nervous lesions, but the efficacy is not improved after increasing the dose. Synonyms: Ethanamide; Acetic Acid Amide; Methanecarboxamide; Acetimidic Acid; Amide C2. Grades: > 98 %. CAS No. 60-35-5. Molecular formula: C2H5NO. Mole weight: 59.07. |  |
| Acid Blue 182 | Acid Blue 182, also known as C.I. Acid Blue 182, is a synthetic dye that belongs to the class of azo dyes. Uses: Acid blue 182 has been extensively studied for its application in various scientific research fields. it is used as a ph indicator in analytical chemistry, where it changes color from blue to red as the ph of the solution decreases. acid blue 182 is also used as a model compound in environmental studies to investigate the fate and transport of azo dyes in soil and water systems. Group: Acid dyes. Alternative Names: Alizarine Fast Blue ERL;C.I. Acid Blue 182;4-[[4-(Acetylmethylamino)-2-sulfophenyl]amino]-1-amino-9,10-dihydro-9,10-dioxo-2-anthracene sulfonic acid disodium salt;Blue HRL. CAS No. 12219-26-0. Molecular formula: C22H14N4Na2O9S2. Mole weight: 606.48. Appearance: Powder. IUPACName: disodium;4-[4-[acetyl(methyl)amino]-2-sulfonatoanilino]-1-amino-9,10-dioxoanthracene-2-sulfonate. Canonical SMILES: CC (=O)N (C)C1=CC (=C (C=C1)NC2=CC (=C (C3=C2C (=O)C4=CC=CC=C4C3=O)N)S (=O) (=O)[O-])S (=O) (=O)[O-]. [Na+]. [Na+]. Catalog: ACM12219260. | |
| Acid phosphatase 1 from Human, recombinant | Acid phosphatase 1, also known as ACP1, belongs to the phosphotyrosine protein family. It functions as an acid phosphatase and a protein tyrosine phosphatase (PTPase) and is present in all human tissues, including adipocytes. This enzyme hydrolyzes protein tyrosine phosphate to protein tyrosine and orthophosphate, and also orthophosphoric monoesters to alcohol and orthophosphate. Group: Enzymes. Synonyms: Acid phosphatase 1; soluble isoform b; ACP1; HAAP; LMW-PTP; Red cell acid phosphatase 1; Adipocyte acid phosphatase. Enzyme Commission Number: EC 3.1.3.2. CAS No. 9001-77-8. Purity: > 95% by SDS-PAGE. Apase. Mole weight: 20.1 kDa (178 aa, 1-158 aa + NT His-Tag). Activity: > 60,000 unit/mg of protein. Storage: Can be stored at 4°C short term (1-2 weeks). For long term storage, aliquot and store at -20°C or -70°C. Avoid repeated freezing and thawing cycles. Form: Liquid. Source: E. coli. Species: Human. Acid phosphatase 1; soluble isoform b; ACP1; HAAP; LMW-PTP; Red cell acid phosphatase 1; Adipocyte acid phosphatase; Acid Phosphatase. Cat No: NATE-1672. |  |
| Acid Red 1 | Acid Red 1. Synonyms: Amido Naphthol Red G, Azophloxine. CAS No. 3734-67-6. Product ID: CDC10-0138. Molecular formula: C18H13N3Na2O8S2. Category: Cosmetic Color Additives. Product Keywords: Cosmetic Ingredients; Cosmetic Color Additives; Acid Red 1; CDC10-0138; 3734-67-6; C18H13N3Na2O8S2; Amido Naphthol Red G, Azophloxine; 223-098-9; MFCD00003954; 3734-67-6. Purity: Dye content 60 %. Color: Very Dark Red. EC Number: 223-098-9. Physical State: Powder. Solubility: Methanol (Slightly), Water (Slightly). Quality Level: 100. Storage: room temp. Boiling Point: N/A. Melting Point: N/A. |  |
| Amaranth | Amaranth is a food pigment additive, which can cause DNA damage difference in colon of rats and mice. Uses: Indicators and reagents. Synonyms: Bordeaux S; 1-(4-Sulfo-1-naphthylazo)-2-naphthol-3,6-disulfonic Acid Trisodium Salt; 1302 Red; 1508 Red; 2-Hydroxy-1,1'-azonaphthalene-3,6,4'-trisulfonic Acid Trisodium Salt; Acid Amaranth; Acid Amaranth I; Acid Amaranth J; Acid Amaranth N; Acid Leather Rubine S; Acid Red 27; Aizen Amaranth; Amaranth A; Amaranth B; Amaranth BPC; Amaranth Extra; Amaranth Lake; Amaranth R; Amaranth S; Amaranth red; Amaranthe; Azo Red R; Azo Rubine SF; Azo Ruby S; Azorubin S. Grades: >95%. CAS No. 915-67-3. Molecular formula: C20H11N2Na3O10S3. Mole weight: 604.47. | |
| β-Nicotinamide-Adenine Dinucleotide, Reduced Form (β-NADH) | NADH is a coenzyme that functions as a regenerating electron donor in catabolic processes including glycolysis, beta-oxidation and the citric acid cycle (Krebs cycle, TCA cycle). It participates in cell signaling events as well, for example as a substrate for the poly (ADP-ribose) polymerases (PARPs) during the DNA damage response. The NAD+/NADH dependent sirtuins play key roles in stress responses during events involving energy metabolism, with implications in cancer biology, diabetes and neurodegenerative disease. Group: Coenzymes. Synonyms. Enzyme Commission Number: EC 1.1.1.1. CAS No. 606-68-8. Purity: Dertermined by decrease in absorbance at 340 nm on enzymatic oxidation with ADH* at pH 10.0 > 95% *ADH = Alcohol dehydrogenase (yeast) (EC 1.1.1.1.). β-NADH. Mole weight: 709.41. Storage: Keep tightly stoppered in the dark below 5°C. Moisture will reduce the purity. For prolonged storage, keep below-20°C. Unstable in acids, but relatively stable at pH 10-11. aldehyde reductase; ADH; alcohol dehydrogenase (NAD); aliphatic alcohol dehydrogenase; ethanol dehydrogenase; NAD-dependent alcohol dehydrogenase; NAD-specific aromatic alcohol dehydrogenase; NADH-alcohol dehydrogenase; NADH-aldehyde dehydrogenase; primary alcohol dehydrogenase; yeast alcohol dehydrogenase; EC 1.1.1.1; β-NADH. Cat No: NATE-0786. | |
| CB-7921220 | CB-7921220 is an adenylate cyclase inhibitor which is selective, reducing adenylyl cyclase type I and VI activity by 60% while having no effect on types II and V in Sf9 membranes stimulated by forskolin at a concentration of 100 μM. CB-7921220 has a binding conformation similar to ATP and P-site inhibitors, which may explain its lack of selectivity between AC1 and AC6. Synonyms: CB7921220; CB 7921220; CB-7921220; 6-[(E)-2-(4-aminophenyl)ethenyl]pyridine-2-carboxylic acid. CAS No. 115453-99-1. Molecular formula: C14H12N2O2. Mole weight: 240.26. | |
| D 358 | D 358. Uses: Photosensitive red-violet dye having excellent photoelectric conversion efficiency. Group: Dye-sensitized solar cell (dssc) materials electronic materials. Alternative Names: 12-[3- (Carboxymethyl)-5-[[4-[4- (2, 2-diphenylvinyl)phenyl]-1, 2, 3, 3a, 4, 8b-hexahydrocyclopenta[b]indol-7-yl]methylene]-4, 4'-dioxo-2'-thioxo-4, 5-dihydro-2'H, 3H-[2, 5'-bithiazolylidene]-3' (4'H)-yl]dodecanoic Acid. CAS No. 1207638-53-6. Product ID: 12-[(5E)-5-[(5E)-3-(carboxymethyl)-5-[[4-[4-(2,2-diphenylethenyl)phenyl]-2,3,3a,8b-tetrahydro-1H-cyclopenta[b]indol-7-yl]methylidene]-4-oxo-1,3-thiazolidin-2-ylidene]-4-oxo-2-sulfanylidene-1,3-thiazolidin-3-yl]dodecanoic acid. Molecular formula: 912.19. Mole weight: C52H53N3O6S3. C1CC2C (C1)N (C3=C2C=C (C=C3)C=C4C (=O)N (C (=C5C (=O)N (C (=S)S5)CCCCCCCCCCCC (=O)O)S4)CC (=O)O)C6=CC=C (C=C6)C=C (C7=CC=CC=C7)C8=CC=CC=C8. InChI=1S/C52H53N3O6S3/c56-46 (57) 23-14-6-4-2-1-3-5-7-15-30-53-50 (61) 48 (64-52 (53) 62) 51-54 (34-47 (58) 59) 49 (60) 45 (63-51) 33-36-26-29-44-42 (32-36) 40-21-16-22-43 (40) 55 (44) 39-27-24-35 (25-28-39) 31-41 (37-17-10-8-11-18-37) 38-19-12-9-13-20-38/h8-13, 17-20, 24-29, 31-33, 40, 43H, 1-7, 14-16, 21-23, 30, 34H2, (H, 56, 57) (H, 58, 59) /b45-33?, 51-48+. HXSDFCKKOUCOIZ-XCSHDWRRSA-N. >95.0%HPLC. | |
| D358 Dye | D358 Dye. Uses: Photosensitive red-violet dye having excellent photoelectric conversion efficiency as a metal-free dye. efficiency of dssc device - η > 6.7%cell area: 0.25 cm2 (0.5 cm × 0.5 cm)tio2 thickness: 5 μmtio2: screen printingelectrolyte: 0.1 m lii; 0.05 m i2; 0.6 m dimethyl propylimidazoliumiodide; 0.05 m t-butylpyridine in 3-methoxypropionitrilelight source: am1.5counter electrode: pt/. Group: Organic solar cell (opv) materials. Alternative Names: 5-[3-(Carboxymethyl)-5-[[4-[4-(2,2-diphenylethenyl)phenyl]-1,2,3,3a,4,8b-hexahydrocyclopent[b]indol-7-yl]methylene]-4-oxo-2-thiazoli dinylidene]-4-oxo-2-thioxo-3-thiazolidinedodecanoic acid. CAS No. 1207638-53-6. Pack Sizes: 100 mg in glass insert. Product ID: 12-[(5E)-5-[(5E)-3-(carboxymethyl)-5-[[4-[4-(2,2-diphenylethenyl)phenyl]-2,3,3a,8b-tetrahydro-1H-cyclopenta[b]indol-7-yl]methylidene]-4-oxo-1,3-thiazolidin-2-ylidene]-4-oxo-2-sulfanylidene-1,3-thiazolidin-3-yl]dodecanoic acid. Molecular formula: 912.2g/mol. Mole weight: C52H53N3O6S3. S=C (S/C1=C2N (CC (O) =O) C (/C (S\2) =C\C (C=C3) =CC4=C3N (C5=CC=C (C=C (C6=CC=CC=C6) C7=CC=CC=C7) C=C5) C8C4CCC8) =O) N (CCCCCCCCCCCC (O) =O) C1=O. 1S/C52H53N3O6S3/c56-46 (57) 23-14-6-4-2-1-3-5-7-15-30-53-50 (61) 48 (64-52 (53) 62) 51-54 (34-47 (58) 59) 49 (60) 45 (63-51) 33-36-26-29-44-42 (32-36) 40-21-16-22-43 (40) 55 (44) 39-27-24-35 (25-28-39) 31-41 (37-17-10-8-11-18-37) 38-19-12-9-13-20-38/h8-13, 17-20, 24-29, 31-33 | |
| dihydrolipoyllysine-residue acetyltransferase | A multimer (24-mer or 60-mer, depending on the source) of this enzyme forms the core of the pyruvate dehydrogenase multienzyme complex, and binds tightly both EC 1.2.4.1, pyruvate dehydrogenase (acetyl-transferring) and EC 1.8.1.4, dihydrolipoyl dehydrogenase. The lipoyl group of this enzyme is reductively acetylated by EC 1.2.4.1, and the only observed direction catalysed by EC 2.3.1.12 is that where the acetyl group is passed to coenzyme A. Group: Enzymes. Synonyms: acetyl-CoA:dihydrolipoamide S-acetyltransferase; dihydrolipoamide S-acetyltransferase; d. Enzyme Commission Number: EC 2.3.1.12. CAS No. 9032-29-5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2058; dihydrolipoyllysine-residue acetyltransferase; EC 2.3.1.12; 9032-29-5; acetyl-CoA:dihydrolipoamide S-acetyltransferase; dihydrolipoamide S-acetyltransferase; dihydrolipoate acetyltransferase; dihydrolipoic transacetylase; dihydrolipoyl acetyltransferase; lipoate acetyltransferase; lipoate transacetylase; lipoic acetyltransferase; lipoic acid acetyltransferase; lipoic transacetylase; lipoylacetyltransferase; thioltransacetylase A; transacetylase X; enzyme-dihydrolipoyllysine:acetyl-CoA S-acetyltransferase; acetyl-CoA:enzyme 6-N-(dihydrolipoyl)lysine S-acetyltransferase. Cat No: EXWM-2058. | |
| disodium 5-((4-acetylamino-2-sulphophenyl)azo)-6-amino-4-hydroxynaphthalene-2-disulphonate | Acid Red 37 is a red synthetic dye that belongs to the acid dye category. It is known for its vibrant red hue and good color fastness properties. Uses: Acid red 37 functions as both a histological dye and a fluorescent dye. Group: Acid dyes. Alternative Names: Acid Fast Red EBL; Dycosacid Red BG; C.I. Acid Red 37; Lerni Acid Red BG; Acid Fast Red B; Acid red BG; Albion Acid Red BG; Acid Light Red 2BL; Red BL; Acid Red 37 (C.I.). CAS No. 6360-7-2. Molecular formula: C18H14N4Na2O11S3. Mole weight: 604.498. Appearance: Powder. Purity: 0.95. Canonical SMILES: [Na+]. [Na+]. CC (=O)Nc1ccc (\N=N\c2c (N)ccc3cc (cc (O)c23)S ([O-]) (=O)=O)c (c1)S ([O-]) (=O)=O. Density: 1.504 g/mL. ECNumber: 228-823-2. Catalog: ACM6360072. | |
| Elsibucol | Elsibucol, a metabolically stable derivative of probucol, inhibits atherosclerosis and preserves endothelial healing following arterial injury. In vitro, elsibucol reduces vascular smooth muscle cell proliferation without affecting cell viability. Synonyms: 4-[2,6-ditert-butyl-4-[2-(3,5-ditert-butyl-4-hydroxyphenyl)sulfanylpropan-2-ylsulfanyl]phenoxy]butanoic acid; (4,2,6-di-tert-butyl-4-(1-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-1-methyl-ethylsulfanyl)-phenoxy-butyric acid); Elsibucol; AGI 1096; AGI1096; AGI-1096; Elsibucol; UNII-O7T92N1Y8T.elsibucol. Grades: >98%. CAS No. 216167-95-2. Molecular formula: C35H54O4S2. Mole weight: 602.94. | |
| Ethyl 4-Bromomethylcinnamate | Used in the preparation of cinnamamide derivative as 5α-reductase inhibitors. Group: Biochemicals. Alternative Names: 3-[4-(Bromomethyl)phenyl]-2-propenoic Acid Ethyl Ester; 4-Bromomethylcinnamic Acid Ethyl Ester; Ethyl p- (Bromomethyl) cinnamate. Grades: Highly Purified. CAS No. 60682-98-6. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| Ethylenediaminetetraacetic acid | Ethylenediaminetetraacetic acid (EDTA) is a kind of metal chelating agent (binds to bivalent and trivalent metal cations, including calcium). Ethylenediaminetetraacetic acid has antibacterial, anti-inflammatory, antioxidant, anti-hypercalcemia and anticoagulant activities. Ethylenediaminetetraacetic acid decreases the metal ion-catalyzed oxidative damage to proteins, and allows maintenance of reducing environment during protein purification. Ethylenediaminetetraacetic acid can alleviate the liver fibrosis. Ethylenediaminetetraacetic acid can be used for coronary artery disease and neural system disease research [1] [2] [3] [4] [5] [6] [7]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: EDTA. CAS No. 60-00-4. Pack Sizes: 500 mg; 1 g. Product ID: HY-Y0682. | |
| Fenofibric Acyl Glucuronide | A derivative of Fenofibrate. Fenofibrate is mainly used to reduce cholesterol levels in patients at risk of cardiovascular disease. Synonyms: Fenofibric acid acyl glucuronide. Grades: > 95%. CAS No. 60318-63-0. Molecular formula: C23H23ClO10. Mole weight: 494.88. | |
| Fmoc-Dab(ivDde)-OH | This orthogonally-protected diaminobutyric acid derivative is based on the hindered Dde variant ivDde. The side-chain ivDde group is considerably more stable to piperidine than Dde and is less prone to migrate from protected to unprotected side-chains and from side-chain to γ-amino group.When removing ivDde in the presence of allyl-based protecting groups, allyl alcohol should be included in the deprotection solution to prevent reduction of the allyl group. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-Dab(ivDde)-OH, N-α-Fmoc-N-γ-1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl-L-diaminobutanoic acid. CAS No. 607366-21-2. Mole weight: 546.65. Catalog: ACM607366212. | |
| Food Red No. 102 | Food Red No. 102. Group: Biochemicals. Alternative Names: 7-Hydroxy-8-[2-(4-sulfo-1-naphthalenyl)diazenyl]-1,3-naphthalenedisulfonic Acid Trisodium Salt; C.I. Acid Red 18; Cochineal Red 4R; New Coccine; Coccin Red; Takaoka Brilliant Scarlet 3R; Triacid Ponceau 4R; Triacid Scarlet 3R; Trisodium 1-(4-sulfo-1-naphthylazo)-2-naphthol-6,8-disulfonate; Vicoacid Scarlet 3R; Victoria Scarlet 3R; Victoria Scarlet Red. Grades: Highly Purified. CAS No. 2611-82-7. Pack Sizes: 5g. Molecular Formula: C20H11N2Na3O10S3, Molecular Weight: 604.47. US Biological Life Sciences. | Worldwide |
| Gallium(III) oxide | Gallium sesquioxide is reduced to gallium suboxide, Ga2O [12024-20-3] by common reducing agents. Also, heating the sesquioxide with gallium metal yields gallium suboxide. Heating with magnesium reduces the oxide to elemental form in a violent reaction: Ga2O3 + 3Mg →2Ga + 3MgO Heating with mineral acids yields corresponding gallium salts. When heated with a mixture of hydrogen and arsenic vapors at 600°C, gallium arsenide, GaAs is produced. When heated with alkali metal oxide at 1,000°C, alkali metal gallates, such as K2Ga2O6 are formed. Group: Nanoparticles & nanopowders. Alternative Names: Digallium trioxide. CAS No. 12024-21-4. Molecular formula: Ga2O3. Mole weight: 187.44. Appearance: White Powder. Purity: 99%, 99.9%, 99.99%, 99.999%. IUPACName: oxo(oxogallanyloxy)gallane. Density: 5.88 g/cm³. Catalog: ACM12024214. | |
| Gemilukast | This active molecular is an potent dual Leukotriene CysLT1 and CysLT2 Receptor antagonist originated by Ono Pharmaceutical. IC50 values is 1.7nM against human CysLT1 and 25 nM against human CysLT2. Gemilukast reduced LTC4-induced bronchoconstriction in asthmatic animal models dose-dependently. In addition, it can also reduceantigen-induced constriction of isolated human bronchi. In 2015, Phase-II clinical trials in Asthma in Japan and USA was on-going. Uses: Asthma. Synonyms: ONO6950; ONO 6950; ONO-6950;4,4'-(4-fluoro-7-((4-(4-(3-fluoro-2-methylphenyl)butoxy)phenyl)ethynyl)-2-methyl-1H-indole-1,3-diyl)dibutyric acid;1232861-64-1 (disodium salt); 1232873-69-6 (8 hydrate and disodium salt). Grades: 98%. CAS No. 1232861-58-3. Molecular formula: C36H37F2NO5. Mole weight: 601.69. | |
| Histone Lysine Demethylase Inhibitor VII, GSK-J1 (3-(6-(4,5-Dihydro-1H-benzo[d]azepin-3(2H)-yl)-2-(pyridin-2-yl)pyrimidin-4-ylamino)propanoic Acid, JHDM Inhibitor II) | A pyridinyl -pyrimidinyl aminopropanoic acid that effectively inhibits KDM6 family H3K27m3 demethylases JMJD3 and UTX (IC50 = 18 and 56uM, respectively, by MALDI Mass detection) in an alpha-ketoglutarate-competitive, peptide substrate-non-competitive manner, displaying much reduced potency against JARID1C, JMJD1a, JMJD2a, JMJD2c, JMJD2d, JMJD2e, as well as112 kinases and 60 non-kinase enzymes. Recommended for cell-free assays only. For culture treatment, use the cell-permeable pro-drug GSK-J4. Group: Biochemicals. Grades: Highly Purified. CAS No. 1373422-53-7. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Isomalt | Isomalt. Synonyms: Hydrogenated isomaltulose; hydrogenated palatinose. CAS No. 64519-82-0. Product ID: PE-0494. Category: Sweetening agent. Product Keywords: Pharmaceutical Excipients; Excipients for Solid Dosage Form; Isomalt; Sweeteners Excipients; Sweetening agent; 64519-82-0; 64519-82-0. UNII: S870P55O2W. Stability and Storage Conditions: Isomalt has very good thermal and chemical stability. When it is melted, no changes in the molecular structure are observed. It exhibits considerable resistance to acids and microbial influences.Isomalt is non-hygroscopic, and at 25°C does not significantly absorb additional water up to a relative humidity (RH) of 85%; paracetamol (acetaminophen) tablets based on isomalt were stored for 6 months at 85% RH at 208C and retained their physical aspect. If stored under normal ambient conditions, isomalt is chemically stable for many years. When it is stored in an unopened container at 20°C and 60% RH, a re-evaluation after 3 years is recommended. Isomalt does not undergo browning reactions; it has no reducing groups, and therefore it does not react with other ingredients in a formulation (e.g. with amines in Maillard reactions). Source and Preparation: Isomalt is produced from food-grade sucrose in a two-stage process.Beet sugar is converted by enzymatic transglucosidation into the reducing disaccharide isomaltulose. This undergoes catalytical hydrogenation to produce isomalt. Safety: Isomal | |
| LACCAIC ACID | LACCAIC ACID. Synonyms: Shellac red color;Red Lac;froM Lacca;Laccaic Acid ;lac dye red;Purple sweet potato pigment;Water-soluble shellac red;c.i.75450. CAS No. 60687-93-6. Pack Sizes: 1 g. Product ID: CDF4-0025. Molecular formula: C91H62N2O44. Category: Color Fixative. Product Keywords: Food Ingredients; Color Fixative; LACCAIC ACID; CDF4-0025; 60687-93-6; C91H62N2O44; 918-731-7; 60687-93-6. Purity: 0.99. Color: Red to Very Dark Red. EC Number: 918-731-7. Physical State: Solid. Solubility: Aqueous Base (Slightly), DMSO (Slightly). Storage: -20°C Freezer, Under inert atmosphere. Application: Laccaic acid is an organic dye with antimicrobial properties towards various pathogenic bacteria and fungi. Laccaic acid is also used as a component of solar cells due to its photoelectric properties. Boiling Point: 453.24°C (rough estimate). Density: 1.4363 (rough estimate). | |
| Linoleic acid | Linoleic acid is a common polyunsaturated (PUFA) found in plant-based oils, nuts and seeds. Linoleic acid is a part of membrane phospholipids, and functions as a structural component to maintain a certain level of membrane fluidity of the transdermal water barrier of the epidermis. Linoleic acid induces red blood cells and hemoglobin damage via oxidative mechanism [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 60-33-3. Pack Sizes: 100 mg; 500 mg; 1 g; 5 g. Product ID: HY-N0729. | |
| Linoleic acid | Linoleic acid is a doubly unsaturated fatty acid widely found in plant glycosides. It exhibits anti-inflammatory, acne reductive, skin-lightening and moisture retentive properties when applied topically on the skin. Synonyms: Linolic acid; Telfairic acid; cis,cis-Linoleic acid. CAS No. 60-33-3. Molecular formula: C18H32O2. Mole weight: 280.45. | |
| Linoleic Acid | Linoleic Acid is anti-inflammatory, acne reductive, and moisture retentive when applied topically on the skin. It is popular in the beauty products industry because of its beneficial properties on the skin. Group: Biochemicals. Alternative Names: (9Z,12Z)-9,12-Octadecadienoic Acid ;(Z,Z)-;9,12-Octadecadienoic Acid; (9Z,12Z)-9,12-Octadecadienoic Acid; (Z,Z)-9,12-Octadecadienoic Acid; (Z,Z)-9,12-Octadecadienoic Acid; 9-cis,12-cis-Linoleic Acid; 9Z,12Z-Linoleic Acid; 9Z,12Z-Octadecadienoic Acid; C18:2; Extra Linoleic 90; Linolic Acid; Polylin 515; Ronacare ASC 3; Unifac 6550; all-cis-9,12-Octadecadienoic Acid; cis,cis-Linoleic Acid; cis-9,cis-12-Octadecadienoic Acid; cis-Δ9,12-Octadecadienoic Acid; α-Linoleic Acid. Grades: Highly Purified. CAS No. 60-33-3. Pack Sizes: 50mg, 100 mg. Molecular Formula: C18H32O2. US Biological Life Sciences. | Worldwide |
| Loxoprofen Sodium | A non-selective nonsteroidal anti-inflammatory drug (NSAID) that has been effective in reducing atherosclerosis in mice by reducing inflammation. It becomes active after metabolism in the body and inhibits the activation of cyclooxygenase. Group: Biochemicals. Alternative Names: α -Methyl-4-[ (2-oxocyclopentyl) methyl]benzeneacetic Acid Sodium Salt; CS 600; Loxonin; Sodium 2- [4- [ (2-Oxocyclopentyl) methyl] phenyl] propionate; Sodium Loxoprofen. Grades: Highly Purified. CAS No. 80382-23-6. Pack Sizes: 25mg. US Biological Life Sciences. | Worldwide |
| Native Pseudomonas sp. p-Hydroxybenzoate Hydroxylase | In enzymology, a 4-hydroxybenzoate 3-monooxygenase (EC 1.14.13.2) is an enzyme that catalyzes the chemical reaction:4-hydroxybenzoate + NADPH + H+ + O2<-> protocatechuate + NADP+ + H2O. The 4 substrates of this enzyme are 4-hydroxybenzoate, NADPH, H+, and O2, whereas its 3 products are protocatechuate, NADP+, and H2O. This enzyme belongs to the family of oxidoreductases, specifically those acting on paired donors, with O2 as oxidant and incorporation or reduction of oxygen. The oxygen incorporated need not be derived from O2 with NADH or NADPH as one donor, and incorporation of one atom o oxygen into the other donor. Applications: This enzyme is useful for enzymatic...p-hydroxybenzoic acid hydroxylase; p-hydroxybenzoic hydroxylase; EC 1.14.13.2; 9059-23-8. Enzyme Commission Number: EC 1.14.13.2. CAS No. 9059-23-8. p-Hydroxybenzoate Hydroxylase. Mole weight: mol wt 55-~60 kDa. Activity: ~20 units/mg solid. Storage: -20°C. Form: lyophilized powder; Contains mannitol and stabilizers. Source: Pseudomonas sp. p-hydroxybenzoate hydrolyase; p-hydroxybenzoate hydroxylase; 4-hydroxybenzoate 3-hydroxylase; 4-hydroxybenzoate monooxygenase; 4-hydroxybenzoic hydroxylase; p-hydroxybenzoate-3-hydroxylase; p-hydroxybenzoic acid hydrolase; p-hydroxybenzoic acid hydroxylase; p-hydroxybenzoic hydroxylase; EC 1.14.13.2; 9059-23-8. Cat No: NATE-0564. | |
| NBI 35965 mesylate | NBI 35965 is a selective corticotropin-releasing factor receptor 1 (CRF1) antagonist without activity against CRF2. It inhibited the stimulation of cAMP induced by sauvagine in CRF1 transfected cells and reduced stress-induced visceral hyperalgesia. Synonyms: (7S)-6-(Cyclopropylmethyl)-2-(2,4-dichlorophenyl)-7-ethyl-7,8-dihydro-4-methyl-6H-1,3,6,8a-tetraazaacenaphthylene monomethanesulfonate; (S)-5-(Cyclopropylmethyl)-1-(2,4-dichlorophenyl)-4-ethyl-7-methyl-4,5-dihydro-3H-2,2a,5,8-tetraazaacenaphthylene methanesulfonic acid. Grades: ≥95%. CAS No. 603151-83-3. Molecular formula: C21H22Cl2N4·CH3SO3H. Mole weight: 497.4. | |
| NLG-919 | NLG919 is an orally available inhibitor of indoleamine 2,3-dioxygenase 1 (IDO1), a cytosolic enzyme responsible for the oxidation of the essential amino acid tryptophan into kynurenine. By inhibiting IDO1 and decreasing kynurenine in tumor cells, this agent increases tryptophan levels, restores the proliferation and activation of various immune cells, including dendritic cells (DCs), natural killer (NK) cells, T-lymphocytes, and causes a reduction in tumor-associated regulatory T-cells (Tregs). Synonyms: GDC0919; GDC-0919; GDC 0919; NLG919; NLG 919; NLG-919; RG6078; RG-6078; RG 6078. Grades: > 98%. CAS No. 1402836-58-1. Molecular formula: C18H22N2O. Mole weight: 282.38. | |
| nNOS - PSD-95 Interaction Inhibitor, ZL006 (5-(3,5-dichloro-2-hydroxybenzylamino)-2-hydroxybenzoic Acid) | A cell-permeable and blood-brain barrier-permeant aminosalicylic acid compound that selectively disrupts nNOS and PSD-95 interaction uponnMDAR activation both in primary murine cortical neurons (0.8- and 2.8-fold increase from basal level with or without 30min 10uM ZL006 pretreatment) in vitro and in mice (0.4- and 1.9-fold increase from basal level with or without inhibitor pretreatment 15min before ischemia; 1.5mg/kg i.v.) in vivo without affecting nNOS activity or non-nNOS-mediated nMDAR EPSCs (excitatory postsynaptic currents). Effectively reduce ischemia-caused brain tissue damage in both mice and rats when applied 1h after blood reperfusion following ishemia (60% and 50% reduction of infarction, respectively; 1.5mg/kg i.v.). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| n-Propyl Alcohol, Reagent Grade, 500 mL | Formula: CH3CH2CH2OH, Formula Wt: 60. 09, Storage Code: Red; flammable. Group: chem-category alcohols. Alternative Names: 1-Propanol; Propylic acid. Grades: chem-grade reagent. CAS No. 71-23-8. Product ID: 884990. -- SOLD FOR EDUCATIONAL USE ONLY -- |  |
| Oxalic acid diammonium monohydrate | Oxalic Acid is a strong dicarboxylic acid occurring in many plants and vegetables and can be used as an analytical reagent and general reducing agent. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: Ethanedioic acid diammonium monohydrate. CAS No. 6009-70-7. Pack Sizes: 1 g; 5 g. Product ID: HY-Y0262A. | |
| Oxantel pamoate | Oxantel Pamoate is used as an anthelmintic. It has typically been used in human and animal field as a standard treatment for intestinal worms. It may be used as a fumarate reductase inhibitor to kill the bacteria responsible for periodontal disease. Uses: Antinematodal agents. Synonyms: (E)-3-(2-(1-methyl-1,4,5,6-tetrahydropyrimidin-2-yl)vinyl)phenol 4,4'-methylenebis(3-hydroxy-2-naphthoate); 4,4'-Methylenebis[3-hydroxy-2-naphthalenecarboxylic Acid 3-[(1E)-2-(1,4,5,6-Tetrahydro-1-methyl-2-pyrimidinyl)ethenyl]phenol; Oxantel Ebonate; Telopar. Grades: 98%. CAS No. 68813-55-8. Molecular formula: C36H32N2O7. Mole weight: 604.65. | |
| Ponalrestat | Ponalrestatis an aldose reductase inhibitor originator byAstraZeneca. It can block the conversion of glucose to sorbitol. Ponalrestatis shows selectivity for aldose reductase 2 over aldose reductase 1 with Ki values of 7.7 nM and 60 μM. Phase III for the treatment of diabetes was discontinued. Uses: Diabetes. Synonyms: Ponalrestat, ICI-128436; ICI 128436; ICI128436; MK-538; MK 538; MK538. Brand name: Statil; Statyl. QJ0339; QJ0339; QJ-0339; 2-(3-(4-bromo-2-fluorobenzyl)-4-oxo-3,4-dihydrophthalazin-1-yl)acetic acid. Grades: 98%. CAS No. 72702-95-5. Molecular formula: C17H12BrFN2O3. Mole weight: 391.20. | |
| PP2A Activating Ligand, ITH12246 | A cell-permeable, relatively non-toxic, 1,8-naphthyridine derived compound that blocks the inhibitory effect of protein phosphatase inhibitors, such as okadaic acid, on protein phosphatase 2A (PP2A). Exhibits blood-brain barrier permeability. Protects neurons against beta-amyloid peptides (Ab1-42) toxicity and okadaic acid-induced tau hyperphosphorylation. Also protects against rotenone and oligomycin A induced neurotoxicity in SH-SY5Y neuroblastoma cells (at ~300nM). Prevents the development of glutamate-induced neuronal lesions in rat hippocampal slices by up-regulating PP2A (~3uM). Shown to reverse the scopolamine-induced memory loss in mice (~10mg/kg i.p) and significantly reduces the infarct volume in an animal model of stroke (~2.5mg/kg). Also acts as an inhibitor of acetylcholinesterase activity in Electrophorus electricus (IC50 = 60nM) and human erythrocytes (IC50 = 780nM). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. Molecular Formula: C??H??N?O?·HCl. US Biological Life Sciences. | Worldwide |
| rac Dihydro Mebendazole | The reduced metabolite of Mebendazole. Group: Biochemicals. Alternative Names: [5-(Hydroxyphenylmethyl)-1H-benzimidazol-2-yl]carbamic Acid. Grades: Highly Purified. CAS No. 60254-95-7. Pack Sizes: 50mg. US Biological Life Sciences. | Worldwide |
| Rac Dihydro Mebendazole | rac Dihydro Mebendazole is the reduced metabolite of Mebendazole. Synonyms: [5-(Hydroxyphenylmethyl)-1H-benzimidazol-2-yl]carbamic Acid Methyl Ester; R 19167. Grades: > 95%. CAS No. 60254-95-7. Molecular formula: C16H15N3O3. Mole weight: 297.31. | |
| Sodium 4-aminosalicylate dihydrate | Sodium 4-aminosalicylate (Sodium para-Aminosalicylic acid) dihydrate is para-aminosalicylic acid (PAS), a dihydrofolate reductase ( DHFR ) inhibitor and antituberculous agent. PAS is incorporated into the folate pathway via dihydropteroate synthase (DHPS) and dihydrofolate synthase (DHFS) to generate the hydroxydihydrofolate antimetabolite, which in turn inhibits DHFR enzyme activity [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 4-Aminosalicylic acid sodium salt dihydrate. CAS No. 6018-19-5. Pack Sizes: 10 mM * 1 mL; 5 g. Product ID: HY-I0447A. | |
| T 98475 | T 98475 is a potent, orally active and non-peptide gonadotropin-releasing hormone (GnRH, LHRH) receptor antagonist (IC50 = 0.2, 4.0 and 60 nM for human, monkey and rat GnRH receptors, respectively). T 98475 inhibits LH release in vitro (IC50 = 100 nM) and reduces plasma LH concentration in castrated male cynomolgus monkeys. Synonyms: Thieno[2,3-b]pyridine-5-carboxylic acid, 7-[(2,6-difluorophenyl)methyl]-4,7-dihydro-2-[4-[(2-methyl-1-oxopropyl)amino]phenyl]-3-[[methyl(phenylmethyl)amino]methyl]-4-oxo-, 1-methylethyl ester; 1-Methylethyl 7-[(2,6-difluorophenyl)methyl]-4,7-dihydro-2-[4-[(2-methyl-1-oxopropyl)amino]phenyl]-3-[[methyl(phenylmethyl)amino]methyl]-4-oxothieno[2,3-b]pyridine-5-carboxylate; Isopropyl 3-((benzyl(methyl)amino)methyl)-7-((2,6-difluorophenyl)methyl)-2-(4-(2-methylpropanoylamino)phenyl)-4-oxo-thieno(2,3-b)pyridine-5-carboxylate. Grades: ≥98% by HPLC. CAS No. 199119-18-1. Molecular formula: C37H37F2N3O4S. Mole weight: 657.77. | |
| Valoneic Acid Dilactone | Valoneic Acid Dilactone is a polyphenol natural product. It shows an inhibitory effect on 5α-reductase. It also has selectively inhibited RNase L and shows antibacterial activity. Synonyms: Valoneic acid bilactone. Grades: 90% by HPLC. CAS No. 60202-70-2. Molecular formula: C21H10O13. Mole weight: 470.3. | |
| Acid red 18 | Reddish powder or granules. Group: Polymers. Product ID: trisodium; 7-hydroxy-8-[(4-sulfonatonaphthalen-1-yl)diazenyl]naphthalene-1,3-disulfonate. Molecular formula: 604.5g/mol. Mole weight: C20H11N2Na3O10S3;C20H11N2Na3O10S3. C1=CC=C2C (=C1)C (=CC=C2S (=O) (=O)[O-])N=NC3=C (C=CC4=CC (=CC (=C43)S (=O) (=O)[O-])S (=O) (=O)[O-])O. [Na+]. [Na+]. [Na+]. InChI=1S/C20H14N2O10S3. 3Na/c23-16-7-5-11-9-12 (33 (24, 25)26)10-18 (35 (30, 31)32)19 (11)20 (16)22-21-15-6-8-17 (34 (27, 28)29)14-4-2-1-3-13 (14)15; ; ; /h1-10, 23H, (H, 24, 25, 26) (H, 27, 28, 29) (H, 30, 31, 32); ; ; /q; 3*+1/p-3. SWGJCIMEBVHMTA-UHFFFAOYSA-K. | |
| AKR1C3 Inhibitor (3- (4- (Trifluoromethyl) phenylamino) benzoic Acid) | A cell-permeable 3-phenyl-aminobenzoate compound that acts as a potent, competitive, reversible, active-site targeting inhibitor of aldo-keto reductase 1C3 (AKR1C3; type 5 17b-hydroxysteroid dehydrogenase) (IC50 = 60nM) with excellent selectivity over other closely related human AKR isoforms (IC50 = 22.7, 15.4, 62.7, >50, and >50uM for and AKR1C1, AKR1C2, AKR1C4, AKR1B1 and AKR1B10, respectively. Exhibits a weak inhibitory effect on cyclooxygenase 1 and 2 (IC50 = 100uM). Shown to efficiently block the AKR1C3-mediated production of testosterone in LNCaP-AKR1C3 cells (~10uM). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 25mg. US Biological Life Sciences. | Worldwide |
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