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| Product | Description | |
|---|---|---|
| 3-Hexylthiophene | 3-Hexylthiophene. Group: Biochemicals. Grades: Highly Purified. CAS No. 1693-86-3. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C10H16S. US Biological Life Sciences. |  Worldwide |
| 3-Hexylthiophene | 3-Hexylthiophene. Group: Electroluminescence materials other electronic materials polymers. CAS No. 1693-86-3. Product ID: 3-hexylthiophene. Molecular formula: 168.3g/mol. Mole weight: C10H16S. CCCCCCC1=CSC=C1. InChI=1S / C10H16S / c1-2-3-4-5-6-10-7-8-11-9-10 / h7-9H, 2-6H2, 1H3. JEDHEMYZURJGRQ-UHFFFAOYSA-N. |  |
| 3-Hexylthiophene | Hexylthiophene. |  Pennsylvania PA |
| 3-Hexylthiophene-2-boronic acid pinacol ester | 3-Hexylthiophene-2-boronic acid pinacol ester. Uses: Reagent used for suzuki-miyaura cross-coupling reactions p-type/n-type switching of ambipolar bithiazole-benzothiadiazole-based polymers in solar cells hierarchical self-assembly of semiconductor functionalized peptide a-helixes and optoelectronic properties reagent used in preparation of photovoltaic materials, polymers, and thiophene-based compounds with photophysical, electrochemical, and fluorescent properties polymer solar cells for low band gap poly(1,4-arylene-2,5-thienylene)s with benzothiadiazole units dithienothiophene-based dyes for dye-sensitized solar cells. Group: Saltsynthetic tools and reagents. Alternative Names: 2-(3-Hexyl-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, 3-Hexyl-2-thienylboronic acid. CAS No. 850881-09-3. Pack Sizes: 1, 5 g in glass bottle. Product ID: 2-(3-hexylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane. Molecular formula: 294.26. Mole weight: C16H27BO2S. CCCCCCc1ccsc1B2OC(C)(C)C(C)(C)O2. 1S / C16H27BO2S / c1-6-7-8-9-10-13-11-12-20-14 (13) 17-18-15 (2, 3) 16 (4, 5) 19-17 / h11-12H, 6-10H2, 1-5H3, XCXAUPBHQCCWCI-UHFFFAOYSA-N. XCXAUPBHQCCWCI-UHFFFAOYSA-N. | |
| 2-Bromo-3-hexylthiophene | 2-Bromo-3-hexylthiophene is a monomeric precursor that forms bromo terminate polymers. It is synthesized by the bromination of hexylthiophene. Uses: 2-bromo-3-hexylthiophene is majorly used in the formation of π-conjugated conductive polymers (cps) for the fabrication of organic field effect transistors (ofets) and organic photovoltaics (opvs). the grignard metathesis (grim) polymerization of 2-bromo-3-hexylthiophene terminates a bromine and a proton at both ends to form conductive poly(3-hexylthiophene) (p3ht). Group: Small molecule semiconductor building blockselectroluminescence materials other electronic materials synthetic tools and reagents polymers. Alternative Names: 2-bromo-3-hexylthiophene; 2-Bromo-3-nonylthiophene; Thiophene,2-broMo-3-hexyl-; 2-Bromo-3-hexylthiophene 97%. CAS No. 69249-61-2. Pack Sizes: Packaging 1, 5 g in glass bottle. Product ID: 2-bromo-3-hexylthiophene. Molecular formula: 247.20. Mole weight: C10H15BrS. CCCCCCc1ccsc1Br. 1S / C10H15BrS / c1-2-3-4-5-6-9-7-8-12-10 (9) 11 / h7-8H, 2-6H2, 1H3. XQJNXCHDODCAJF-UHFFFAOYSA-N. >98.0%(GC). | |
| Poly(3-hexylthiophene-2, 5-diyl) | Poly(3-hexylthiophene-2, 5-diyl). Group: Polystyrene (ps). CAS No. 156074-98-5. Product ID: 2,5-dibromo-3-hexylthiophene. CCCCCCC1=C(SC(=C1)Br)Br. InChI=1S / C10H14Br2S / c1-2-3-4-5-6-8-7-9 (11) 13-10 (8) 12 / h7H, 2-6H2, 1H3. NSYFIAVPXHGRSH-UHFFFAOYSA-N. | |
| Poly(3-hexylthiophene-2,5-diyl) | Metal purity: Mg: ≤100 ppm Ni: ≤100 ppm. Group: Bioelectronic materials organic field effect transistor (ofet) materials organic light-emitting diode (oled) materials. Alternative Names: P3HT. CAS No. 104934-50-1. Molecular formula: Mw 20,000-45,000. Mole weight: (C10H14S)n. | |
| Poly(3-hexylthiophene-2,5-diyl) | Poly(3-hexylthiophene-2,5-diyl) (P3HT) is a poly(alkylthiophene) based semiconducting polymer that is hydrophobic at neutral state and has π-π conjugation in its backbone. It has a hole mobility is in the range of 10-3-10-1 cm2V-1s-1 and is commonly used in the development of field-effect transistors (FETs) for a wide range of applications. Poly(3-hexylthiophene) (P3HT) is a regioregular semiconducting polymer. It is used in organic electronics primarily because of its regular end-to-end arrangement of side chain, which allows efficient p- p stacking of the conjugated backbones. On account of the alkyl side group, P3HT is rendered hydrophobic in neutral state. Solution-to-solid phase transformation and thin film formation of poly(3-hexylthiophene) (P3HT) was reported in a study. Uses: Rechargeable battery electrodes, electrochromic devices, chemical and optical sensors, light-emitting diodes, microelectrical amplifiers, field-effect transistors and non-linear optical materials. for the characterization and solid-state properties of this polymer, see j. am. chem. soc. p3ht, an electron donor that acts as a semiconducting active layer in combination with an electron acceptor li. Group: 3d printing materials bioelectronic materials organic field effect transistor (ofet) materials organic light-emitting diode (oled) materials. Alternative Names: P3HT. CAS No. 156074-98-5. Pack Sizes: 1 g in glass bottle. | |
| Poly(3-hexylthiophene-2,5-diyl), ≥95% | Poly(3-hexylthiophene-2,5-diyl), ≥95%. Group: Electronic chemicals. CAS No. 125321-66-6. Product ID: 3-hexyl-2-[4-hexyl-5-(4-hexyl-5-methylthiophen-2-yl)thiophen-2-yl]-5-methylthiophene. Molecular formula: 528.9g/mol. Mole weight: C32H48S3. CCCCCCC1=C (SC (=C1)C)C2=CC (=C (S2)C3=CC (=C (S3)C)CCCCCC)CCCCCC. InChI=1S / C32H48S3 / c1-6-9-12-15-18-26-22-29 (34-25 (26) 5) 32-28 (20-17-14-11-8-3) 23-30 (35-32) 31-27 (21-24 (4) 33-31) 19-16-13-10-7-2 / h21-23H, 6-20H2, 1-5H3. JKARVMUJJLUQDW-UHFFFAOYSA-N. | |
| Poly(3-hexylthiophene-2,5-diyl) (regioregular) | Poly(3-hexylthiophene-2,5-diyl) (regioregular). Group: Small molecule semiconductor building blocksdye-sensitized solar cell (dssc) materials organic field effect transistor (ofet) materials organic semiconductorsorganic solar cell (opv) materials perovskite solar cell (psc) materials polymers. CAS No. 125321-66-6. Product ID: 3-hexyl-2-[4-hexyl-5-(4-hexyl-5-methylthiophen-2-yl)thiophen-2-yl]-5-methylthiophene. Molecular formula: 528.9g/mol. Mole weight: C32H48S3. CCCCCCC1=C (SC (=C1)C)C2=CC (=C (S2)C3=CC (=C (S3)C)CCCCCC)CCCCCC. InChI=1S / C32H48S3 / c1-6-9-12-15-18-26-22-29 (34-25 (26) 5) 32-28 (20-17-14-11-8-3) 23-30 (35-32) 31-27 (21-24 (4) 33-31) 19-16-13-10-7-2 / h21-23H, 6-20H2, 1-5H3. JKARVMUJJLUQDW-UHFFFAOYSA-N. | |
| 2-(3-Hexyl-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | 2-(3-Hexyl-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2-(3-Hexyl-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;3-Hexylthiophene-2-boronicacidpinacolester;3-Hexyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene;3-Hexyl-2-thienylboronic acid;2-(3-Hexyl-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxabo. Product Category: Organic & Printed Electronics. CAS No. 850881-09-3. Molecular formula: C16H27BO2S. Mole weight: 294.26. Purity: 0.95. IUPACName: 2-(3-hexylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane. Canonical SMILES: B1(OC(C(O1)(C)C)(C)C)C2=C(C=CS2)CCCCCC. Density: 0.983. Product ID: ACM850881093. Alfa Chemistry ISO 9001:2015 Certified. |  |
| 3-Hexyl-thiophene | 3-Hexyl-thiophene. Group: Organic light-emitting diode (oled) materials. CAS No. 1693-86-3. Product ID: 3-hexylthiophene. Molecular formula: 168.3g/mol. Mole weight: C10H16S. CCCCCCC1=CSC=C1. InChI=1S / C10H16S / c1-2-3-4-5-6-10-7-8-11-9-10 / h7-9H, 2-6H2, 1H3. JEDHEMYZURJGRQ-UHFFFAOYSA-N. | |
| Hexadecane | Hexadecane may be used as a solvent for trioctylamine-based synthesis of indium antimonide (InSb) nanocrystals. It may also be used as an internal standard for the synthesis of poly(9,9-dioctylfluorene)-b-poly(3-hexylthiophene) via Grignard metathesis chain growth polymerization. Uses: Used as a solvent and organic intermediate. Synonyms: Cetane. Grades: 95%. CAS No. 544-76-3. Molecular formula: C16H34. Mole weight: 226.44. |  |
| ICBA | ICBA is a C60 derivative that can be synthesized from C60 and indene. It is an acceptor material with shallow lowest occupied molecular orbital(LUMO) which can be used to enhance the performance of polymeric solar cells(PSCs). Uses: Icba can be used with poly(3-hexylthiophene)(p3ht) as an active layer which can be used in the fabrication of organic solar cells(oscs).icba in combination with thiazolo-thiazolo can be used as a donor. it can be blended with pcbm for photovoltaic based application. Group: 3d printing materials carbon nano materials dye-sensitized solar cell (dssc) materials electronic materials organic field effect transistor (ofet) materials organic solar cell (opv) materials. Alternative Names: 1', 1'', 4', 4''-Tetrahydro-di[1, 4]methanonaphthaleno[1, 2:2', 3', 56, 60:2'', 3''][5, 6]fullerene-C60, C60 derivative, indene-C60 bisadduct. CAS No. 1207461-57-1. Pack Sizes: 250 mg in glass insert. Molecular formula: 952.99. Mole weight: C78H16. C1C2C3= CC= CC= C3C1C45C26C7= C8C9= C1C2= C3C% 10= C9C9= C% 11C% 12= C% 10C% 10= C% 13C% 14= C% 12C% 12= C% 15C% 16= C (C4= C4C% 17= C% 16C% 16= C% 18C% 19= C% 17C% 17= C% 20C% 21= C% 19C% 19= C% 22C% 23= C% 21C% 21= C (C1= C7C (= C% 21% 20) C6= C% 174) C2= C% 23C (= C3% 10) C% 221C% 13 (C2CC1C1= CC= CC= C21) C (= C% 18% 19) C% 14= C% 15% 16) C (= C% 12% 11) C5= C98. InChI=1S/C78H16/c1-2-6-12-11 (5-1) 15-9-16 (12) 76-69-53-37-23-25-41-29 (37) 30-38-24-26-42 (30) 58-57 (41) 73-65-49 ( | |
| Nickel(II) bromide ethylene glycol dimethyl ether complex | Nickel(II) bromide ethylene glycol dimethyl ether complex is a nickel-based catalyst that is used in the preparation of poly(3-hexylthiophene) (P3HT) Kumada catalyst transfer polymerization. It facilitates good control over the molecular weight of the conjugating polymer. Uses: Transition metal catalysts. Synonyms: Nickel, dibromo[1,2-di(methoxy-κO)ethane]-; Dibromo[1,2-di(methoxy-κO)ethane]nickel; Nickel, dibromo(1,2-dimethoxyethane)-; Nickel, dibromo(1,2-dimethoxyethane-O,O')-; (1,2-Dimethoxyethane)nickel dibromide; 1,2-Dimethoxyethane nickel(II) bromide; Dibromo(1,2-dimethoxyethane)nickel; Dibromo(1,2-dimethoxyethane)nickel(II); Dibromo(glyme)nickel; NiBr2(dme); Nickel(II) dimethoxyethane bromide; Dimethoxyethane Nickel(II) dibromide. Grades: ≥95%. CAS No. 28923-39-9. Molecular formula: C4H10Br2NiO2. Mole weight: 308.62. | |
| 3,3'''-Dihexyl-2,2':5',2'':5'',2'''-quaterthiophene | 3,3'''-Dihexyl-2,2':5',2'':5'',2'''-quaterthiophene (D4HT) is a dihexyl quarterthiophene derivative that can be used as a donor-acceptor molecule in organic electronic devices. It has a field mobility of 0.23 cm2/Vs and acts as an active layer in semiconductors. Uses: D4ht can be used a conjugating polymer in the fabrication of devices such as organic field effect transistor (ofet), organic thin film transistor (otft) and organic photovoltaics (opv). Group: Organic field effect transistor (ofet) materials synthetic tools and reagents. Alternative Names: 5,5'-Bis(3-hexyl-2-thienyl)-2,2'-bithiophene, α, ω-Dihexylquaterthiophene, DH-4T. CAS No. 132814-91-6. Pack Sizes: Packaging 1 g in glass bottle. Product ID: 2-(3-hexylthiophen-2-yl)-5-[5-(3-hexylthiophen-2-yl)thiophen-2-yl]thiophene. Molecular formula: 498.83. Mole weight: C28H34S4. CCCCCCc1ccsc1-c2ccc(s2)-c3ccc(s3)-c4sccc4CCCCCC. 1S / C28H34S4 / c1-3-5-7-9-11-21-17-19-29-27 (21) 25-15-13-23 (31-25) 24-14-16-26 (32-24) 28-22 (18-20-30-28) 12-10-8-6-4-2 / h13-20H, 3-12H2, 1-2H3. MLDVGCCQHBDHDR-UHFFFAOYSA-N. | |
| 3,3'''-Dihexyl-2,2':5',2'':5'',2'''-quaterthiophene (contains 3% Dichloromethane at maximum) | 3,3'''-Dihexyl-2,2':5',2'':5'',2'''-quaterthiophene (contains 3% Dichloromethane at maximum). Group: Small molecule semiconductor building blockspolymers. CAS No. 132814-91-6. Product ID: 2-(3-hexylthiophen-2-yl)-5-[5-(3-hexylthiophen-2-yl)thiophen-2-yl]thiophene. Molecular formula: 498.8g/mol. Mole weight: C28H34S4. CCCCCCC1=C (SC=C1)C2=CC=C (S2)C3=CC=C (S3)C4=C (C=CS4)CCCCCC. InChI=1S / C28H34S4 / c1-3-5-7-9-11-21-17-19-29-27 (21) 25-15-13-23 (31-25) 24-14-16-26 (32-24) 28-22 (18-20-30-28) 12-10-8-6-4-2 / h13-20H, 3-12H2, 1-2H3. MLDVGCCQHBDHDR-UHFFFAOYSA-N. | |
| 3,3'-Dihexyl-2,2'-bithiophene | 3,3'-Dihexyl-2,2'-bithiophene. Group: Electroluminescence materials polymers. CAS No. 125607-30-9. Product ID: 3-hexyl-2-(3-hexylthiophen-2-yl)thiophene. Molecular formula: 334.6g/mol. Mole weight: C20H30S2. CCCCCCC1=C(SC=C1)C2=C(C=CS2)CCCCCC. InChI=1S / C20H30S2 / c1-3-5-7-9-11-17-13-15-21-19 (17) 20-18 (14-16-22-20) 12-10-8-6-4-2 / h13-16H, 3-12H2, 1-2H3. RQHMOXZEVWCNMG-UHFFFAOYSA-N. | |
| 3-Hexyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene | 3-Hexyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene. Group: Small molecule semiconductor building blockselectroluminescence materials polymerssemiconductor blocks. CAS No. 850881-09-3. Product ID: 2-(3-hexylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane. Molecular formula: 294.3g/mol. Mole weight: C16H27BO2S. B1 (OC (C (O1) (C)C) (C)C)C2=C (C=CS2)CCCCCC. InChI=1S / C16H27BO2S / c1-6-7-8-9-10-13-11-12-20-14 (13) 17-18-15 (2, 3) 16 (4, 5) 19-17 / h11-12H, 6-10H2, 1-5H3. XCXAUPBHQCCWCI-UHFFFAOYSA-N. | |
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