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| Product | Description | |
|---|---|---|
| NPD, 98.0% | NPD, 98.0%. Group: Printed electronic materials. CAS No. 123847-85-8. Product ID: N-[4-[4-(N-naphthalen-1-ylanilino)phenyl]phenyl]-N-phenylnaphthalen-1-amine. Molecular formula: 588.7g/mol. Mole weight: C44H32N2. C1=CC=C (C=C1) N (C2=CC=C (C=C2) C3=CC=C (C=C3) N (C4=CC=CC=C4) C5=CC=CC6=CC=CC=C65) C7=CC=CC8=CC=CC=C87. InChI=1S/C44H32N2/c1-3-17-37 (18-4-1) 45 (43-23-11-15-35-13-7-9-21-41 (35) 43) 39-29-25-33 (26-30-39) 34-27-31-40 (32-28-34) 46 (38-19-5-2-6-20-38) 44-24-12-16-36-14-8-10-22-42 (36) 44/h1-32H. IBHBKWKFFTZAHE-UHFFFAOYSA-N. |  |
| α-NPD | α-NPD. Group: Organic light-emitting diode (oled) materials. CAS No. 495416-60-9. Product ID: N-[3-methyl-4-[2-methyl-4-(N-naphthalen-1-ylanilino)phenyl]phenyl]-N-phenylnaphthalen-1-amine. Molecular formula: 616.8g/mol. Mole weight: C46H36N2. CC1=C (C=CC (=C1) N (C2=CC=CC=C2) C3=CC=CC4=CC=CC=C43) C5=C (C=C (C=C5) N (C6=CC=CC=C6) C7=CC=CC8=CC=CC=C87) C. InChI=1S/C46H36N2/c1-33-31-39 (47 (37-19-5-3-6-20-37) 45-25-13-17-35-15-9-11-23-43 (35) 45) 27-29-41 (33) 42-30-28-40 (32-34 (42) 2) 48 (38-21-7-4-8-22-38) 46-26-14-18-36-16-10-12-24-44 (36) 46/h3-32H, 1-2H3. ZJFKMIYGRJGWIB-UHFFFAOYSA-N. | |
| 1-Cyanoethyl (diethylamino)dimethylsilane | Heterocyclic Organic Compound. Alternative Names: 1-CYANOETHYL (DIETHYLAMINO)DIMETHYLSILANE; 1-CYANOETHYLDIMETHYL (DIETHYLAMINO)SILANE; Silylatinggrfornpdandms; 1-CYANOETHYL (DIETHYLAMINO)DIMETHYLSILANE [SILYLATING GR FOR NPD AND MS] 95+%. CAS No. 102636-22-6. Molecular formula: C9H20N2Si. Mole weight: 184.35. Catalog: ACM102636226. |  |
| 3-Methylbiphenyl | 3-Methylbiphenyl. Group: other electronic materials. Alternative Names: 3-Methylbiphenyl, 3-Phenyltoluene, Biphenyl, 3-methyl-, 1,1-Biphenyl, 3-methyl-, P36401_ALDRICH, 3-METHYL-1,1-BIPHENYL, EINECS 211-404-3, FR-2285, ST5405258, TL8004559, 643-93-6, InChI=1/C13H12/c1-11-6-5-9-13 (10-11)12-7-3-2-4-8-12/h2-10H, 1H. CAS No. 643-93-6. Product ID: 1-methyl-3-phenylbenzene. Molecular formula: 168.24. Mole weight: C13H12. CC1=CC=CC(=C1)C2=CC=CC=C2. NPDIDUXTRAITDE-UHFFFAOYSA-N. 98%. | |
| Fenhexamid | Fenhexamid is an anti-botrytis fungicide widely used against a broad spectrum of fungi in agricultural crops. Its mode of action involves the inhibition of sterol biosynthesis. Fenhexamid may be used as a standard in the determination of fenhexamid in: Fruits using enzyme-linked immunosorbent assay (ELISA). Tomatoes, grape and wine samples using high-performance liquid chromatography coupled with ultraviolet detector and gas chromatography (GC) coupled with detectors such as nitrogen-phosphorus detector (NPD), electron capture detector (ECD) and ion trap mass spectrometry (ITMS). Group: Biochemicals. Alternative Names: N- (2, 3-Dichloro-4-hydroxyphenyl) -1- methyl cyclohexane carboxamide; Decree; Elevate; KBR 2738; Teldor. CAS No. 126833-17-8. Pack Sizes: 250mg, 500mg, 1g. Molecular Formula: C??H??Cl?NO?, Molecular Weight: 302.2. US Biological Life Sciences. |  Worldwide |
| Native Bothrops atrox Phosphodiesterase I | Phosphodiesterase I breaks phosphodiester bonds and catalyzes the hydrolysis of various nucleotide polyphosphates. Phosphodiesterase I is released from eucaryotic plasma membranes by phosphatidylinositol-specific phospholipase C. Group: Enzymes. Synonyms: Phosphodiesterase I; EC 3.1.4.1; 5'-exonuclease; 5'-phosphodiesterase; 5'-nucleotide phosphodiesterase; oligonucleate 5'-nucleotidohydrolase; 5' nucleotide phosphodiesterase/alkaline phosphodiesterase I; 5'-NPDase; 5'-PDase; 5'-PDE; 5'NPDE; alkaline phosphodiesterase; nucleotide pyrophosphatase/phosphodiesterase I; orthophosphoric diester phosphohydrolase; PDE I; phosphodiesterase; exonuclease I. Enzyme Commission Number: EC 3.1.4.1. CAS No. 9025-82-5. PDE. Activity: > 0.01 unit/mg solid. Storage: -20°C. Form: crude dried venom. Source: Bothrops atrox. Phosphodiesterase I; EC 3.1.4.1; 5'-exonuclease; 5'-phosphodiesterase; 5'-nucleotide phosphodiesterase; oligonucleate 5'-nucleotidohydrolase; 5' nucleotide phosphodiesterase/alkaline phosphodiesterase I; 5'-NPDase; 5'-PDase; 5'-PDE; 5'NPDE; alkaline phosphodiesterase; nucleotide pyrophosphatase/phosphodiesterase I; orthophosphoric diester phosphohydrolase; PDE I; phosphodiesterase; exonuclease I. Cat No: NATE-0511. |  |
| Native Crotalus adamanteus venom Phosphodiesterase I | Venom exonuclease (Phosphodiesterase I) successively hydrolyzes 5'-mononucleotides from 3'-OH-terminated ribo- and deoxyribo-oligonucleotides. The enzyme has an optimal pH range of 9.8-10.4 and a molecular weight of 115 kDa. Phosphodiesterase is inhibited by reducing agents such as glutathione, cysteine and ascorbic acids. It is completely inhibited by 5mM EDTA while ATP, ADP and AMP are partial inhibitors. The enzyme has an absolute requirement for Mg2+. Group: Enzymes. Synonyms: Phosphodiesterase I; EC 3.1.4.1; 5'-exonuclease; 5'-phosphodiesterase; 5'-nucleotide phosphodiesterase; oligonucleate 5'-nucleotidohydrolase; 5' nucleotide phosphodiesterase/alkaline phosphodiesterase I; 5'-NPDase; 5'-PDase; 5'-PDE; 5'NPDE; alkaline phosphodies. Enzyme Commission Number: EC 3.1.4.1. CAS No. 9025-82-5. PDE. Activity: > 20 units per mg dry weight. Storage: -20°C. Form: Lyophilized in vials. Source: Crotalus adamanteus venom. Phosphodiesterase I; EC 3.1.4.1; 5'-exonuclease; 5'-phosphodiesterase; 5'-nucleotide phosphodiesterase; oligonucleate 5'-nucleotidohydrolase; 5' nucleotide phosphodiesterase/alkaline phosphodiesterase I; 5'-NPDase; 5'-PDase; 5'-PDE; 5'NPDE; alkaline phosphodiesterase; nucleotide pyrophosphatase/phosphodiesterase I; orthophosphoric diester phosphohydrolase; PDE I; phosphodiesterase; exonuclease I. Cat No: NATE-0512. | |
| Native Crotalus atrox (Western Diamondback Rattlesnake) Phosphodiesterase I | Phosphodiesterase I breaks phosphodiester bonds and catalyzes the hydrolysis of various nucleotide polyphosphates. Phosphodiesterase I is released from eucaryotic plasma membranes by phosphatidylinositol-specific phospholipase C. Applications: Phosphodiesterase (pde) is any enzyme that is used to breaks phosphodiester bonds. phosphodiesterase i from western diamondback rattlesnake, is used in phosphodiesterase activation assays for calmodulin. it is added to hydrolyze amp. it is a membrane-bound glycoprotein that is used to catalyze the hydrolysis of various nucleotide polyphosphates. Group: Enzymes. Synonyms: Phosphodiesterase I; EC 3.1.4.1; 5'-exonuclease; 5'-phosphodiesterase; 5'-nucleotide phosphodi. Enzyme Commission Number: EC 3.1.4.1. CAS No. 9025-82-5. PDE. Activity: > 0.01 unit/mg solid. Storage: -20°C. Form: crude dried venom. Source: Crotalus atrox (Western Diamondback Rattlesnake). Phosphodiesterase I; EC 3.1.4.1; 5'-exonuclease; 5'-phosphodiesterase; 5'-nucleotide phosphodiesterase; oligonucleate 5'-nucleotidohydrolase; 5' nucleotide phosphodiesterase/alkaline phosphodiesterase I; 5'-NPDase; 5'-PDase; 5'-PDE; 5'NPDE; alkaline phosphodiesterase; nucleotide pyrophosphatase/phosphodiesterase I; orthophosphoric diester phosphohydrolase; PDE I; phosphodiesterase; exonuclease I. Cat No: NATE-0513. | |
| N, N'-Di(1-naphthyl)-N, N'-diphenyl-(1, 1'-biphenyl)-4, 4'-diamine | TGA/DSC Lot specific traces available upon request. Uses: Hole transporting material for oled devices. Group: Organic light-emitting diode (oled) materials sublimed materials other materials. Alternative Names: N, N'-Bis(naphthalen-1-yl)-N, N'-bis(phenyl)benzidine, NPB, NPD. CAS No. 123847-85-8. Pack Sizes: 5 g in glass bottle. Product ID: N-[4-[4-(N-naphthalen-1-ylanilino)phenyl]phenyl]-N-phenylnaphthalen-1-amine. Molecular formula: 588.74. Mole weight: C44H32N2. c1ccc (cc1) N (c2ccc (cc2) -c3ccc (cc3) N (c4ccccc4) c5cccc6ccccc56) c7cccc8ccccc78. 1S/C44H32N2/c1-3-17-37 (18-4-1) 45 (43-23-11-15-35-13-7-9-21-41 (35) 43) 39-29-25-33 (26-30-39) 34-27-31-40 (32-28-34) 46 (38-19-5-2-6-20-38) 44-24-12-16-36-14-8-10-22-42 (36) 44/h1-32H, IBHBKWKFFTZAHE-UHFFFAOYSA-N. IBHBKWKFFTZAHE-UHFFFAOYSA-N. | |
| N,N'-Di-1-naphthyl-N,N'-diphenylbenzidine | N,N'-Di-1-naphthyl-N,N'-diphenylbenzidine. Group: Organic light-emitting diode (oled) materials perovskite solar cell (psc) materials. Alternative Names: α-NPB α-NPD. CAS No. 123847-85-8. Product ID: N-[4-[4-(N-naphthalen-1-ylanilino)phenyl]phenyl]-N-phenylnaphthalen-1-amine. Molecular formula: 588.75. Mole weight: C44H32N2. C1=CC=C (C=C1) N (C2=CC=C (C=C2) C3=CC=C (C=C3) N (C4=CC=CC=C4) C5=CC=CC6=CC=CC=C65) C7=CC=CC8=CC=CC=C87. InChI=1S/C44H32N2/c1-3-17-37 (18-4-1) 45 (43-23-11-15-35-13-7-9-21-41 (35) 43) 39-29-25-33 (26-30-39) 34-27-31-40 (32-28-34) 46 (38-19-5-2-6-20-38) 44-24-12-16-36-14-8-10-22-42 (36) 44/h1-32H. IBHBKWKFFTZAHE-UHFFFAOYSA-N. >98.0%HPLC. | |
| N,N'-Di-1-naphthyl-N,N'-diphenylbenzidine (purified by sublimation) | N,N'-Di-1-naphthyl-N,N'-diphenylbenzidine (purified by sublimation). Group: Semiconducting materials other material building blockselectroluminescence materials organic light-emitting diode (oled) materials perovskite solar cell (psc) materials. Alternative Names: α-NPB (purified by sublimation) α-NPD (purified by sublimation). CAS No. 123847-85-8. Product ID: N-[4-[4-(N-naphthalen-1-ylanilino)phenyl]phenyl]-N-phenylnaphthalen-1-amine. Molecular formula: 588.75. Mole weight: C44H32N2. C1=CC=C (C=C1) N (C2=CC=C (C=C2) C3=CC=C (C=C3) N (C4=CC=CC=C4) C5=CC=CC6=CC=CC=C65) C7=CC=CC8=CC=CC=C87. InChI=1S/C44H32N2/c1-3-17-37 (18-4-1) 45 (43-23-11-15-35-13-7-9-21-41 (35) 43) 39-29-25-33 (26-30-39) 34-27-31-40 (32-28-34) 46 (38-19-5-2-6-20-38) 44-24-12-16-36-14-8-10-22-42 (36) 44/h1-32H. IBHBKWKFFTZAHE-UHFFFAOYSA-N. >99.0%(HPLC)(N). | |
| PDI-DPP-PDI | Band gap: 1.6 eV. Group: Organic field effect transistor (ofet) materials organic solar cell (opv) materials. Alternative Names: Perylene diimide flanked diketopyrrolopyrrole,nPDI2DPP. CAS No. 2083628-79-7. O=C1C (C2=C (C3=CC=C (C4=CC (C (N (C (CC) CC) C5=O) =O) =C (C5=CC (N6CCCCCC) =C78) C7=C4C9=CC=C%10C%11=C (C (N (C (CC) CC) C%10=O) =O) C=C6C8=C9%11) S3) N1CCCCCCCC) =C (C%12=CC=C (C%13=CC (C (N (C (CC) CC) C%14=O) =O) =C (C%14=CC (N%15CCCCCC) =C%16%17) C%16=C%13C%18=CC=C%19C%20=C (C (N (C (CC) CC) C%. | |
| phosphodiesterase I | Hydrolyses both ribonucleotides and deoxyribonucleotides. Has low activity towards polynucleotides. A 3'-phosphate terminus on the substrate inhibits hydrolysis. Group: Enzymes. Synonyms: 5'-exonuclease; 5'-phosphodiesterase; 5'-nucleotide phosphodiesterase; oligonucleate 5'-nucleotidohydrolase; 5' nucleotide phosphodiesterase/alkaline phosphodiesterase I; 5'-NPDase; 5'-PDase; 5'-PDE; 5'NPDE; alkaline phosphodiesterase; nucleotide pyrophosphatase/phosphodiesterase I; orthophosphoric diester phosphohydrolase; PDE I; phosphodiesterase (ambiguous); exonuclease I. Enzyme Commission Number: EC 3.1.4.1. CAS No. 9025-82-5. PDE. 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-3710; phosphodiesterase I; EC 3.1.4.1; 9025-82-5; 5'-exonuclease; 5'-phosphodiesterase; 5'-nucleotide phosphodiesterase; oligonucleate 5'-nucleotidohydrolase; 5' nucleotide phosphodiesterase/alkaline phosphodiesterase I; 5'-NPDase; 5'-PDase; 5'-PDE; 5'NPDE; alkaline phosphodiesterase; nucleotide pyrophosphatase/phosphodiesterase I; orthophosphoric diester phosphohydrolase; PDE I; phosphodiesterase (ambiguous); exonuclease I. Cat No: EXWM-3710. | |
| Protectin D1 | Protectin D1, a neuroprotectin D1 produced by neuronal cells, is a member of a newly discovered family of bioactive products derived from docosahexaenoic acid. Protectin D1 also serves as a specialized pro-resolving mediator, exhibiting effective in vivo pro-resolving activity in various human disease models. Additionally, Protectin D1 is an inhibitor of NALP3 inflammasomes and regulates the PI3K/AKT and HIF-1α signaling pathways. Protectin D1 exerts anti-inflammatory effects by reducing ROS levels, inhibiting the expression of NALP3 , ASC , and Caspase-1 , and consequently decreasing the release of pro-inflammatory cytokines IL-1β and IL-18. Furthermore, Protectin D1 enhances miRNA-210 expression, activates the PI3K/AKT signaling pathway, and exerts cardioprotective effects. Protectin D1 holds promise for research in cardiovascular diseases and inflammatory disorders [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Neuroprotectin D1; NPD1. CAS No. 660430-03-5. Pack Sizes: 10 μg (138.7 μM * 200 μL in ethanol). Product ID: HY-130413. |  |
| Tween 60 | Tween 60, also known as polysorbate 60, polyoxyethylene sorbitan monostearate, its molecular formula is C64H126O26. In general, it is a lemon-colored to orange oily liquid or semi-gel, with a slight special odor and a slightly bitter taste. Tween 60 is soluble in water, aniline, ethyl acetate and toluene, but insoluble in mineral oil and vegetable oil. Tween 60 has excellent emulsifying properties, and has the functions of wetting, foaming, and diffusion, and is widely used in textiles, medicine, water-based coatings and other industries. Group: Polymers. Alternative Names: Polyoxyethylene-60-sorbitan monostearate. CAS No. 9005-67-8. Pack Sizes: 1 kgs/drum,25 kgs/drum or as your requirements. Product ID: [(2R)-2-[(2R,3R,4S)-3,4-bis(2-hydroxyethoxy)oxolan-2-yl]-2-hydroxyethyl] dodecanoate. Molecular formula: 1311.70. Mole weight: C64H126O26. InChI=1S / C22H42O8 / c1-2-3-4-5-6-7-8-9-10-11-20 (26) 29-16-18 (25) 21-22 (28-15-13-24) 19 (17-30-21) 27-14-12-23 / h18-19, 21-25H, 2-17H2, 1H3 / t18-, 19+, 21-, 22- / m1 / s1. CRBBOOXGHMTWOC-NPDDRXJXSA-N. | |
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