Alfa Chemistry Materials 5 - Products
Alfa Chemistry Materials is specialized in material chemistry and offers an extensive catalog of materials in a wide range of applications, including Metals and Materials, 3D Printing Materials, Biomaterials.
| Product | Description | |
|---|---|---|
| 4arm-PEG40K-Succinimidyl Carboxymethyl Ester | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 4arm-PEG-Succinimidyl Carboxymethyl Ester. Molecular formula: average Mn 40000. |  |
| 4arm-PEG40K-Succinimidyl Glutarate | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 4arm-PEG-Succinimidyl Glutarate. Molecular formula: average Mn 40000. | |
| 4arm-PEG40K-Succinimidyl Succinate | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 4arm-PEG-Succinimidyl Succinate. Molecular formula: average Mn 40000. | |
| 4arm-PEG5K 1arm-OH, 3arm-COOH | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Molecular formula: average Mn 5000. | |
| 4arm-PEG5K 3arm-OH, 1arm-COOH | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Molecular formula: average Mn 5000. | |
| 4arm-PEG5K-COOH | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 4arm-PEG-COOH, 4arm-PEG-Carboxyl. Molecular formula: average Mn 5000. | |
| 4arm-PEG5K-NH2 | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 4arm-PEG-NH2, 4arm-PEG-amine. Molecular formula: average Mn 5000. | |
| 4arm-PEG5K-SH | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 4arm-PEG-SH. Molecular formula: average Mn 5000. | |
| 4arm-PEG5K-Succinimidyl Carboxymethyl Ester | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: 4arm-PEG-Succinimidyl Carboxymethyl Ester. Molecular formula: average Mn 5000. | |
| 4arm-PEG GPC Standards | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| 4-arm Poly(ethylene glycol) norbornene terminated | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: PEG-norbornene, PEG-nb. CAS No. 1191287-92-9. Pack Sizes: Packaging 1 g in glass bottle. Molecular formula: average Mn 10000. | |
| 4'-Benzyloxyacetophenone | 4'-Benzyloxyacetophenone. Group: Liquid crystal (lc) building blocksliquid crystal (lc) materials. CAS No. 54696-05-8. Product ID: 1-(4-phenylmethoxyphenyl)ethanone. Molecular formula: 226.27g/mol. Mole weight: C15H14O2. CC(=O)C1=CC=C(C=C1)OCC2=CC=CC=C2. InChI=1S/C15H14O2/c1-12 (16) 14-7-9-15 (10-8-14) 17-11-13-5-3-2-4-6-13/h2-10H, 11H2, 1H3. MKYMYZJJFMPDOA-UHFFFAOYSA-N. | |
| 4-Benzyloxybenzaldehyde | 4-Benzyloxybenzaldehyde. Group: Liquid crystal (lc) building blocks. CAS No. 4397-53-9. Product ID: 4-phenylmethoxybenzaldehyde. Molecular formula: 212.25. Mole weight: C14H12O2. C1=CC=C(C=C1)COC2=CC=C(C=C2)C=O. InChI=1S/C14H12O2/c15-10-12-6-8-14 (9-7-12) 16-11-13-4-2-1-3-5-13/h1-10H, 11H2. ZVTWZSXLLMNMQC-UHFFFAOYSA-N. | |
| 4-Benzyloxybenzoic Acid | 4-Benzyloxybenzoic Acid. Group: Liquid crystal (lc) building blocksliquid crystal (lc) materials. CAS No. 1486-51-7. Product ID: 4-phenylmethoxybenzoic acid. Molecular formula: 228.25. Mole weight: C14H12O3. C1=CC=C(C=C1)COC2=CC=C(C=C2)C(=O)O. InChI=1S/C14H12O3/c15-14 (16)12-6-8-13 (9-7-12)17-10-11-4-2-1-3-5-11/h1-9H, 10H2, (H, 15, 16). AQSCHALQLXXKKC-UHFFFAOYSA-N. >98.0%(GC)(T). | |
| 4-(Biphenyl-4-yl)-6-(4-bromophenyl)-2-phenylpyrimidine | 4-(Biphenyl-4-yl)-6-(4-bromophenyl)-2-phenylpyrimidine. Group: Small molecule semiconductor building blockssemiconductor blocks. CAS No. 1421599-34-9. Product ID: 4-(4-bromophenyl)-2-phenyl-6-(4-phenylphenyl)pyrimidine. Molecular formula: 463.38. Mole weight: C28H19BrN2. C1=CC=C (C=C1)C2=CC=C (C=C2)C3=CC (=NC (=N3)C4=CC=CC=C4)C5=CC=C (C=C5)Br. InChI=1S/C28H19BrN2/c29-25-17-15-23 (16-18-25)27-19-26 (30-28 (31-27)24-9-5-2-6-10-24)22-13-11-21 (12-14-22)20-7-3-1-4-8-20/h1-19H. VSCGHXGRCSQGIE-UHFFFAOYSA-N. >98.0%(HPLC). | |
| 4-Biphenyl Benzoate | 4-Biphenyl Benzoate. Group: Liquid crystal (lc) building blocks. CAS No. 2170-13-0. Product ID: (4-phenylphenyl) benzoate. Molecular formula: 274.3g/mol. Mole weight: C19H14O2. C1=CC=C (C=C1)C2=CC=C (C=C2)OC (=O)C3=CC=CC=C3. InChI=1S/C19H14O2/c20-19 (17-9-5-2-6-10-17)21-18-13-11-16 (12-14-18)15-7-3-1-4-8-15/h1-14H. CINHWMYRCOGYIX-UHFFFAOYSA-N. | |
| 4-Biphenylboronic Acid, (contains varying amounts of Anhydride) | 4-Biphenylboronic Acid, (contains varying amounts of Anhydride). Group: Electroluminescence materials. CAS No. 5122-94-1. Product ID: (4-phenylphenyl)boronic acid. Molecular formula: 198.03g/mol. Mole weight: C12H11BO2. B(C1=CC=C(C=C1)C2=CC=CC=C2)(O)O. InChI=1S/C12H11BO2/c14-13 (15)12-8-6-11 (7-9-12)10-4-2-1-3-5-10/h1-9, 14-15H. XPEIJWZLPWNNOK-UHFFFAOYSA-N. | |
| 4-[Bis(4-iodophenyl)amino]benzaldehyde | 4-[Bis(4-iodophenyl)amino]benzaldehyde. Group: Small molecule semiconductor building blockssemiconductor blocks. CAS No. 808758-81-8. Product ID: 4-(4-iodo-N-(4-iodophenyl)anilino)benzaldehyde. Molecular formula: 525.1g/mol. Mole weight: C19H13I2NO. C1=CC (=CC=C1C=O)N (C2=CC=C (C=C2)I)C3=CC=C (C=C3)I. InChI=1S/C19H13I2NO/c20-15-3-9-18 (10-4-15)22 (19-11-5-16 (21)6-12-19)17-7-1-14 (13-23)2-8-17/h1-13H. HIUBJHKIRVFTOM-UHFFFAOYSA-N. | |
| 4-[Bis(4-methoxyphenyl)amino]benzaldehyde | 4-[Bis(4-methoxyphenyl)amino]benzaldehyde. Group: Small molecule semiconductor building blocks other electronic materials semiconductor blocks. CAS No. 89115-20-8. Product ID: 4-(4-methoxy-N-(4-methoxyphenyl)anilino)benzaldehyde. Molecular formula: 333.4g/mol. Mole weight: C21H19NO3. COC1=CC=C (C=C1)N (C2=CC=C (C=C2)C=O)C3=CC=C (C=C3)OC. InChI=1S/C21H19NO3/c1-24-20-11-7-18 (8-12-20)22 (17-5-3-16 (15-23)4-6-17)19-9-13-21 (25-2)14-10-19/h3-15H, 1-2H3. CTRXZOLNEVJBDX-UHFFFAOYSA-N. | |
| [4-[Bis(4-methoxyphenyl)amino]phenyl]boronic Acid (contains varying amounts of Anhydride) | [4-[Bis(4-methoxyphenyl)amino]phenyl]boronic Acid (contains varying amounts of Anhydride). Group: Small molecule semiconductor building blocks. CAS No. 201802-29-1. Product ID: [4-(4-methoxy-N-(4-methoxyphenyl)anilino)phenyl]boronic acid. Molecular formula: 349.2g/mol. Mole weight: C20H20BNO4. B (C1=CC=C (C=C1)N (C2=CC=C (C=C2)OC)C3=CC=C (C=C3)OC) (O)O. InChI=1S/C20H20BNO4/c1-25-19-11-7-17 (8-12-19)22 (18-9-13-20 (26-2)14-10-18)16-5-3-15 (4-6-16)21 (23)24/h3-14, 23-24H, 1-2H3. HDVVFJKYLNSKOG-UHFFFAOYSA-N. | |
| 4-Bromo-1-naphthaleneboronic Acid (contains varying amounts of Anhydride) | 4-Bromo-1-naphthaleneboronic Acid (contains varying amounts of Anhydride). Group: Small molecule semiconductor building blocks. CAS No. 145965-14-6. Product ID: (4-bromonaphthalen-1-yl)boronic acid. Molecular formula: 250.89g/mol. Mole weight: C10H8BBrO2. B(C1=CC=C(C2=CC=CC=C12)Br)(O)O. InChI=1S/C10H8BBrO2/c12-10-6-5-9 (11 (13)14)7-3-1-2-4-8 (7)10/h1-6, 13-14H. DKKOMUVRCPKTFX-UHFFFAOYSA-N. | |
| 4'-Bromo-2,2':6',2''-terpyridine | 4'-Bromo-2,2':6',2''-terpyridine. Group: Ligands for functional metal complexes. Alternative Names: 4'-Bromo-α, α', α''-tripyridyl. CAS No. 149817-62-9. Product ID: 4-bromo-2,6-dipyridin-2-ylpyridine. Molecular formula: 312.16. Mole weight: C15H10BrN3. C1=CC=NC (=C1)C2=CC (=CC (=N2)C3=CC=CC=N3)Br. CJRRILXBSCRHKN-UHFFFAOYSA-N. InChI=1S/C15H10BrN3/c16-11-9-14 (12-5-1-3-7-17-12)19-15 (10-11)13-6-2-4-8-18-13/h1-10H. 97%. | |
| 4-Bromo-2,2'-bipyridyl | 4-Bromo-2,2'-bipyridyl. Group: Ligands for functional metal complexes. Alternative Names: 4-bromo-2-pyridin-2-ylpyridine. CAS No. 14162-95-9. Product ID: 4-bromo-2-pyridin-2-ylpyridine. Molecular formula: 235.08. Mole weight: C10H7BrN2. C1=CC=NC(=C1)C2=NC=CC(=C2)Br. InChI=1S/C10H7BrN2/c11-8-4-6-13-10 (7-8)9-3-1-2-5-12-9/h1-7H. SCOXFIBXWCCICG-UHFFFAOYSA-N. 97%+. | |
| 4-Bromo-2-thiophenecarboxylic Acid | 4-Bromo-2-thiophenecarboxylic Acid. Group: Electroluminescence materials polymers. CAS No. 16694-18-1. Product ID: 4-bromothiophene-2-carboxylic acid. Molecular formula: 207.05g/mol. Mole weight: C5H3BrO2S. C1=C(SC=C1Br)C(=O)O. InChI=1S/C5H3BrO2S/c6-3-1-4 (5 (7)8)9-2-3/h1-2H, (H, 7, 8). HJZFPRVFLBBAMU-UHFFFAOYSA-N. | |
| 4-Bromo-2-(trimethylsilyl)thiophene | 4-Bromo-2-(trimethylsilyl)thiophene. Group: Small molecule semiconductor building blockssemiconductor blocks. CAS No. 77998-61-9. Product ID: (4-bromothiophen-2-yl)-trimethylsilane. Molecular formula: 235.22g/mol. Mole weight: C7H11BrSSi. C[Si](C)(C)C1=CC(=CS1)Br. InChI=1S/C7H11BrSSi/c1-10(2, 3)7-4-6(8)5-9-7/h4-5H, 1-3H3. PHSJATTVQJWOPL-UHFFFAOYSA-N. | |
| 4-Bromo-4'-(4-bromophenyl)-3',5',6'-triphenyl-1,1':2',1''-terphenyl | 4-Bromo-4'-(4-bromophenyl)-3',5',6'-triphenyl-1,1':2',1''-terphenyl. Group: Small molecule semiconductor building blockscarbon nano materials dendrimer building blocks. CAS No. 22932-54-3. Product ID: 1,4-bis(4-bromophenyl)-2,3,5,6-tetraphenylbenzene. Molecular formula: 692.5g/mol. Mole weight: C42H28Br2. C1=CC=C (C=C1) C2=C (C (=C (C (=C2C3=CC=C (C=C3) Br) C4=CC=CC=C4) C5=CC=CC=C5) C6=CC=C (C=C6) Br) C7=CC=CC=C7. InChI=1S/C42H28Br2/c43-35-25-21-33 (22-26-35)41-37 (29-13-5-1-6-14-29)38 (30-15-7-2-8-16-30)42 (34-23-27-36 (44)28-24-34)40 (32-19-11-4-12-20-32)39 (41)31-17-9-3-10-18-31/h1-28H. WGIOZVUGESOGBD-UHFFFAOYSA-N. | |
| 4-Bromo-4'-(4-bromophenyl)-3',5',6'-triphenyl-1,1':2',1''-terphenyl, ≥98% | 4-Bromo-4'-(4-bromophenyl)-3',5',6'-triphenyl-1,1':2',1''-terphenyl, ≥98%. Group: Carbon nano materials. CAS No. 22932-54-3. Product ID: 1,4-bis(4-bromophenyl)-2,3,5,6-tetraphenylbenzene. Molecular formula: 692.5g/mol. Mole weight: C42H28Br2. C1=CC=C (C=C1) C2=C (C (=C (C (=C2C3=CC=C (C=C3) Br) C4=CC=CC=C4) C5=CC=CC=C5) C6=CC=C (C=C6) Br) C7=CC=CC=C7. InChI=1S/C42H28Br2/c43-35-25-21-33 (22-26-35)41-37 (29-13-5-1-6-14-29)38 (30-15-7-2-8-16-30)42 (34-23-27-36 (44)28-24-34)40 (32-19-11-4-12-20-32)39 (41)31-17-9-3-10-18-31/h1-28H. WGIOZVUGESOGBD-UHFFFAOYSA-N. | |
| 4-Bromo-4',4''-dimethoxytriphenylamine | 4-Bromo-4',4''-dimethoxytriphenylamine. Group: Small molecule semiconductor building blockssemiconductor blocks. CAS No. 194416-45-0. Product ID: N-(4-bromophenyl)-4-methoxy-N-(4-methoxyphenyl)aniline. Molecular formula: 384.3g/mol. Mole weight: C20H18BrNO2. COC1=CC=C (C=C1)N (C2=CC=C (C=C2)OC)C3=CC=C (C=C3)Br. InChI=1S / C20H18BrNO2 / c1-23-19-11-7-17 (8-12-19) 22 (16-5-3-15 (21) 4-6-16) 18-9-13-20 (24-2) 14-10-18 / h3-14H, 1-2H3. XXCDCFFPMMCPEE-UHFFFAOYSA-N. | |
| 4-Bromo-4',4''-dimethyltriphenylamine | 4-Bromo-4',4''-dimethyltriphenylamine. Group: Small molecule semiconductor building blockselectroluminescence materials synthetic tools and reagents polymers. Alternative Names: 4-Bromo-N,N-bis(4-methylphenyl)benzenamine. CAS No. 58047-42-0. Pack Sizes: 1, 5 g in glass bottle. Product ID: N-(4-bromophenyl)-4-methyl-N-(4-methylphenyl)aniline. Molecular formula: 352.3g/mol. Mole weight: C20H18BrN. Cc1ccc (cc1)N (c2ccc (C)cc2)c3ccc (Br)cc3. 1S/C20H18BrN/c1-15-3-9-18 (10-4-15)22 (19-11-5-16 (2)6-12-19)20-13-7-17 (21)8-14-20/h3-14H, 1-2H3. YMNJJMJHTXGFOR-UHFFFAOYSA-N. | |
| 4'-Bromo-4-biphenylboronic Acid (contains varying amounts of Anhydride) | 4'-Bromo-4-biphenylboronic Acid (contains varying amounts of Anhydride). Group: Liquid crystal (lc) building blockssmall molecule semiconductor building blocks. Alternative Names: 4-(4-Bromophenyl)phenylboronic Acid (contains varying amounts of Anhydride). CAS No. 480996-05-2. Product ID: [4-(4-bromophenyl)phenyl]boronic acid. Molecular formula: 276.92. Mole weight: C12H10BBrO2. B(C1=CC=C(C=C1)C2=CC=C(C=C2)Br)(O)O. InChI=1S/C12H10BBrO2/c14-12-7-3-10 (4-8-12)9-1-5-11 (6-2-9)13 (15)16/h1-8, 15-16H. HQAGDFJHKPSZHT-UHFFFAOYSA-N. | |
| 4-Bromo-4'-Chloro-1,1'-biphenyl | 4-Bromo-4'-Chloro-1,1'-biphenyl. Group: Small molecule semiconductor building blocks. Alternative Names: 1-Bromo-4-(4-chlorophenyl)benzene. CAS No. 23055-77-8. Product ID: 1-bromo-4-(4-chlorophenyl)benzene. Molecular formula: 267.55. Mole weight: C12H8BrCl. C1=CC(=CC=C1C2=CC=C(C=C2)Br)Cl. InChI=1S/C12H8BrCl/c13-11-5-1-9 (2-6-11)10-3-7-12 (14)8-4-10/h1-8H. WMXVUHANYJZYHO-UHFFFAOYSA-N. 99%+. | |
| 4-Bromo-4'-[di(p-tolyl)amino]stilbene | 4-Bromo-4'-[di(p-tolyl)amino]stilbene. Group: Small molecule semiconductor building blockssemiconductor blocks. CAS No. 101186-77-0. Product ID: N-[4-[2-(4-bromophenyl)ethenyl]phenyl]-4-methyl-N-(4-methylphenyl)aniline. Molecular formula: 454.4g/mol. Mole weight: C28H24BrN. CC1=CC=C (C=C1)N (C2=CC=C (C=C2)C)C3=CC=C (C=C3)C=CC4=CC=C (C=C4)Br. InChI=1S/C28H24BrN/c1-21-3-15-26 (16-4-21)30 (27-17-5-22 (2)6-18-27)28-19-11-24 (12-20-28)8-7-23-9-13-25 (29)14-10-23/h3-20H, 1-2H3. UDHCDVGKGPSNLA-UHFFFAOYSA-N. | |
| 4'-Bromo-4-mercaptobiphenyl | 4'-Bromo-4-mercaptobiphenyl. Group: Self-assembly materials. CAS No. 220805-21-0. | |
| 4-Bromo-4'-phenyltriphenylamine | 4-Bromo-4'-phenyltriphenylamine. Group: Small molecule semiconductor building blocks. CAS No. 503299-24-9. Product ID: N-(4-bromophenyl)-N,4-diphenylaniline. Molecular formula: 400.3g/mol. Mole weight: C24H18BrN. C1=CC=C (C=C1)C2=CC=C (C=C2)N (C3=CC=CC=C3)C4=CC=C (C=C4)Br. InChI=1S/C24H18BrN/c25-21-13-17-24 (18-14-21)26 (22-9-5-2-6-10-22)23-15-11-20 (12-16-23)19-7-3-1-4-8-19/h1-18H. AFDFEVPHXYRVDH-UHFFFAOYSA-N. | |
| 4-Bromo-4'-Propylbiphenyl | 4-Bromo-4'-Propylbiphenyl. Group: Liquid crystal (lc) building blocksliquid crystal (lc) materials. Alternative Names: 4-Bromo-4'-Propyl-Biphenyl. CAS No. 58743-81-0. Product ID: 1-bromo-4-(4-propylphenyl)benzene. Molecular formula: 275.18. Mole weight: C15H15Br. CCCC1=CC=C(C=C1)C2=CC=C(C=C2)Br. InChI=1S/C15H15Br/c1-2-3-12-4-6-13 (7-5-12)14-8-10-15 (16)11-9-14/h4-11H, 2-3H2, 1H3. DPERLOMMOVDOHH-UHFFFAOYSA-N. 98%+. | |
| 4-Bromo-5'-phenyl-1,1':3',1''-terphenyl | 4-Bromo-5'-phenyl-1,1':3',1''-terphenyl. Group: Small molecule semiconductor building blockssemiconductor blocks. Alternative Names: 5'-(4-Bromophenyl)-1,1':3',1''-terphenyl. CAS No. 116941-52-7. Product ID: 1-(4-bromophenyl)-3,5-diphenylbenzene. Molecular formula: 385.3. Mole weight: C24H17Br. C1=CC=C (C=C1)C2=CC (=CC (=C2)C3=CC=C (C=C3)Br)C4=CC=CC=C4. InChI=1S/C24H17Br/c25-24-13-11-20 (12-14-24)23-16-21 (18-7-3-1-4-8-18)15-22 (17-23)19-9-5-2-6-10-19/h1-17H. SIAJAYFLPBYCOF-UHFFFAOYSA-N. >98.0%(GC). | |
| 4-Bromo-9,9-dimethylfluorene | 4-Bromo-9,9-dimethylfluorene. Group: Small molecule semiconductor building blockssemiconductor blocks. CAS No. 942615-32-9. Product ID: 4-bromo-9,9-dimethylfluorene. Molecular formula: 273.17g/mol. Mole weight: C15H13Br. CC1(C2=C(C3=CC=CC=C31)C(=CC=C2)Br)C. InChI=1S/C15H13Br/c1-15 (2)11-7-4-3-6-10 (11)14-12 (15)8-5-9-13 (14)16/h3-9H, 1-2H3. SXOUNESKHJIXNK-UHFFFAOYSA-N. | |
| 4-Bromo-9,9-diphenylfluorene | 4-Bromo-9,9-diphenylfluorene. Group: Small molecule semiconductor building blocksorganic light-emitting diode (oled) materials semiconductor blocks. CAS No. 713125-22-5. Product ID: 4-bromo-9,9-diphenylfluorene. Molecular formula: 397.31. Mole weight: C25H17Br. C1=CC=C (C=C1)C2 (C3=C (C4=CC=CC=C42)C (=CC=C3)Br)C5=CC=CC=C5. InChI=1S / C25H17Br / c26-23-17-9-16-22-24 (23) 20-14-7-8-15-21 (20) 25 (22, 18-10-3-1-4-11-18) 19-12-5-2-6-13-19 / h1-17H. PBWATBVKPGTOTB-UHFFFAOYSA-N. 95%+. | |
| 4-Bromo-9,9'-spirobi[9H-fluorene] | 4-Bromo-9,9'-spirobi[9H-fluorene]. Group: Small molecule semiconductor building blocksorganic light-emitting diode (oled) materials semiconductor blocks. Alternative Names: 4-Bromo-9,9'-Spirobi[Fluorene]. CAS No. 1161009-88-6. Product ID: 4-bromo-9,9'-spirobi[fluorene]. Molecular formula: 395.29. Mole weight: C25H15Br. C1=CC=C2C (=C1)C3=CC=CC=C3C24C5=C (C6=CC=CC=C46)C (=CC=C5)Br. InChI=1S / C25H15Br / c26-23-15-7-14-22-24 (23) 18-10-3-6-13-21 (18) 25 (22) 19-11-4-1-8-16 (19) 17-9-2-5-12-20 (17) 25 / h1-15H. GQXFSXMUBDPXBG-UHFFFAOYSA-N. 95%+. | |
| 4-Bromo-9H-fluoren-9-one | 4-Bromo-9H-fluoren-9-one. Group: Small molecule semiconductor building blocksorganic light-emitting diode (oled) materials semiconductor blocks. CAS No. 4269-17-4. Product ID: 4-bromofluoren-9-one. Molecular formula: 259.1g/mol. Mole weight: C13H7BrO. C1=CC=C2C(=C1)C3=C(C2=O)C=CC=C3Br. InChI=1S/C13H7BrO/c14-11-7-3-6-10-12 (11)8-4-1-2-5-9 (8)13 (10)15/h1-7H. YWYZCXNQMZOYHM-UHFFFAOYSA-N. | |
| 4-broMo-9-phenyl-9H-carbazole | 4-broMo-9-phenyl-9H-carbazole. Group: Small molecule semiconductor building blocksorganic light-emitting diode (oled) materials. Alternative Names: Bromo-N-Phenylcarbazole. CAS No. 1097884-37-1. Product ID: 4-bromo-9-phenylcarbazole. Molecular formula: 322.2. Mole weight: C18H12BrN. C1=CC=C (C=C1)N2C3=C (C4=CC=CC=C42)C (=CC=C3)Br. InChI=1S / C18H12BrN / c19-15-10-6-12-17-18 (15) 14-9-4-5-11-16 (14) 20 (17) 13-7-2-1-3-8-13 / h1-12H. OLLJKISFWSJGID-UHFFFAOYSA-N. 95%+. | |
| 4-Bromoaniline | P-bromoaniline is a brown solid with a sweet odor. (NTP, 1992);COLOURLESS CRYSTALS. Group: Liquid crystal (lc) building blocks. Alternative Names: 4-Bromobenzenamine. CAS No. 106-40-1. Product ID: 4-bromoaniline. Molecular formula: 172.02. Mole weight: C6H6BrN. C1=CC(=CC=C1N)Br. InChI=1S/C6H6BrN/c7-5-1-3-6 (8)4-2-5/h1-4H, 8H2. WDFQBORIUYODSI-UHFFFAOYSA-N. | |
| 4-Bromobenz[a]anthracene | 4-Bromobenz[a]anthracene. Group: Small molecule semiconductor building blocks. CAS No. 61921-39-9. Product ID: 4-bromobenzo[a]anthracene. Molecular formula: 307.2g/mol. Mole weight: C18H11Br. C1=CC=C2C=C3C (=CC2=C1)C=CC4=C3C=CC=C4Br. InChI=1S/C18H11Br/c19-18-7-3-6-15-16 (18)9-8-14-10-12-4-1-2-5-13 (12)11-17 (14)15/h1-11H. ILVKEMDEUCXCAB-UHFFFAOYSA-N. | |
| 4-Bromobenzaldehyde | 4-Bromobenzaldehyde. Group: Liquid crystal (lc) building blocks. CAS No. 1122-91-4. Product ID: 4-bromobenzaldehyde. Molecular formula: 185.02. Mole weight: C7H5BrO. C1=CC(=CC=C1C=O)Br. InChI=1S/C7H5BrO/c8-7-3-1-6 (5-9)2-4-7/h1-5H. ZRYZBQLXDKPBDU-UHFFFAOYSA-N. >97.0%(GC). | |
| 4'-Bromobenzo-18-crown 6-Ether | 4'-Bromobenzo-18-crown 6-Ether. Group: Macrocyclessupramolecular host materials. CAS No. 75460-28-5. Product ID: 20-bromo-2,5,8,11,14,17-hexaoxabicyclo[16.4.0]docosa-1(18),19,21-triene. Molecular formula: 391.25g/mol. Mole weight: C16H23BrO6. C1COCCOCCOC2=C(C=CC(=C2)Br)OCCOCCO1. InChI= 1S / C16H23BrO6 / c17-14-1-2-15-16 (13-14) 23-12-10-21-8-6-19-4-3-18-5-7-20-9-11 -22-15 / h1-2, 13H, 3-12H2. XHHZIFBFFGIFNI-UHFFFAOYSA-N. | |
| 4-Bromocarbazole | 4-Bromocarbazole. Group: Small molecule semiconductor building blockssemiconductor blocks. CAS No. 3652-89-9. Product ID: 4-bromo-9H-carbazole. Molecular formula: 246.1g/mol. Mole weight: C12H8BrN. C1=CC=C2C(=C1)C3=C(N2)C=CC=C3Br. InChI=1S/C12H8BrN/c13-9-5-3-7-11-12 (9)8-4-1-2-6-10 (8)14-11/h1-7, 14H. CBJHFGQCHKNNJY-UHFFFAOYSA-N. | |
| 4-Bromodibenzofuran | 4-Bromodibenzofuran. Group: Small molecule semiconductor building blocksorganic light-emitting diode (oled) materials. CAS No. 89827-45-2. Product ID: 4-bromodibenzofuran. Molecular formula: 247.09. Mole weight: C12H7BrO. C1=CC=C2C(=C1)C3=C(O2)C(=CC=C3)Br. InChI=1S / C12H7BrO / c13-10-6-3-5-9-8-4-1-2-7-11 (8) 14-12 (9) 10 / h1-7H. DYTYBRPMNQQFFL-UHFFFAOYSA-N. >98.0%(GC). | |
| 4-Bromodibenzothiophene | 4-Bromodibenzothiophene. Group: Small molecule semiconductor building blocksorganic light-emitting diode (oled) materials other electronic materials semiconductor blocks. CAS No. 97511-05-2. Product ID: 4-bromodibenzothiophene. Molecular formula: 263.15g/mol. Mole weight: C12H7BrS. C1=CC=C2C(=C1)C3=C(S2)C(=CC=C3)Br. InChI=1S / C12H7BrS / c13-10-6-3-5-9-8-4-1-2-7-11 (8) 14-12 (9) 10 / h1-7H. GJXAVNQWIVUQOD-UHFFFAOYSA-N. | |
| 4-(Bromomethyl)-4'-methyl-2,2'-bipyridyl | 4-(Bromomethyl)-4'-methyl-2,2'-bipyridyl. Group: Ligands for functional metal complexes. Alternative Names: 2-[4-(Bromomethyl)pyridin-2-yl]-4-methylpyridine. CAS No. 81998-05-2. Product ID: 2-[4-(bromomethyl)pyridin-2-yl]-4-methylpyridine. Molecular formula: 263.13. Mole weight: C12H11BrN2. CC1=CC(=NC=C1)C2=NC=CC(=C2)CBr. InChI=1S/C12H11BrN2/c1-9-2-4-14-11 (6-9)12-7-10 (8-13)3-5-15-12/h2-7H, 8H2, 1H3. HUJZHWSADZZJAB-UHFFFAOYSA-N. 97%+. | |
| 4-Bromo-N,N-bis(9,9-dimethyl-9H-fluoren-2-yl)aniline | 4-Bromo-N,N-bis(9,9-dimethyl-9H-fluoren-2-yl)aniline. Group: Small molecule semiconductor building blockssemiconductor blocks. CAS No. 313050-71-4. Product ID: N-(4-bromophenyl)-N-(9,9-dimethylfluoren-2-yl)-9,9-dimethylfluoren-2-amine. Molecular formula: 556.5g/mol. Mole weight: C36H30BrN. CC1 (C2=CC=CC=C2C3=C1C=C (C=C3)N (C4=CC=C (C=C4)Br)C5=CC6=C (C=C5)C7=CC=CC=C7C6 (C)C)C. InChI=1S/C36H30BrN/c1-35 (2) 31-11-7-5-9-27 (31) 29-19-17-25 (21-33 (29) 35) 38 (24-15-13-23 (37) 14-16-24) 26-18-20-30-28-10-6-8-12-32 (28) 36 (3, 4) 34 (30) 22-26/h5-22H, 1-4H3. MNEGWIHTGPUATA-UHFFFAOYSA-N. | |
| 4-Bromophenol | 4-Bromophenol. Group: Liquid crystal (lc) building blocks. Product ID: 4-bromophenol. Molecular formula: 173.01g/mol. Mole weight: C6H5BrO. C1=CC(=CC=C1O)Br. InChI=1S/C6H5BrO/c7-5-1-3-6 (8)4-2-5/h1-4, 8H. GZFGOTFRPZRKDS-UHFFFAOYSA-N. | |
| 4-Bromophenylboronic Acid (contains varying amounts of Anhydride) | 4-Bromophenylboronic Acid (contains varying amounts of Anhydride). Group: Liquid crystal (lc) building blocks. Alternative Names: 4-Bromobenzeneboronic Acid (contains varying amounts of Anhydride). CAS No. 5467-74-3. Product ID: (4-bromophenyl)boronic acid. Molecular formula: 200.83. Mole weight: C6H6BBrO2. B(C1=CC=C(C=C1)Br)(O)O. InChI=1S/C6H6BBrO2/c8-6-3-1-5 (2-4-6)7 (9)10/h1-4, 9-10H. QBLFZIBJXUQVRF-UHFFFAOYSA-N. | |
| (4-Bromophenyl)diphenylphosphine oxide | (4-Bromophenyl)diphenylphosphine oxide. Group: Ligands for functional metal complexessmall molecule semiconductor building blocks other electronic materials. Alternative Names: MFCD00411450; 5525-40-6; PCYBTUUJXASDIX-UHFFFAOYSA-N; (4-Bromophenyl)diphenylphosphine oxide; ZINC140799219; AK552962. CAS No. 5525-40-6. Product ID: 1-bromo-4-diphenylphosphorylbenzene. Molecular formula: 357.187g/mol. Mole weight: C18H14BrOP. C1=CC=C (C=C1)P (=O) (C2=CC=CC=C2)C3=CC=C (C=C3)Br. InChI=1S/C18H14BrOP/c19-15-11-13-18 (14-12-15) 21 (20, 16-7-3-1-4-8-16) 17-9-5-2-6-10-17/h1-14H. PCYBTUUJXASDIX-UHFFFAOYSA-N. | |
| 4-Bromo-P-Terphenyl | 4-Bromo-P-Terphenyl. Group: Small molecule semiconductor building blockselectroluminescence materials other electronic materials. Alternative Names: 4-BroMoterphenyl. CAS No. 1762-84-1. Product ID: 1-bromo-4-(4-phenylphenyl)benzene. Molecular formula: 309.2. Mole weight: C18H13Br. C1=CC=C (C=C1)C2=CC=C (C=C2)C3=CC=C (C=C3)Br. InChI=1S/C18H13Br/c19-18-12-10-17 (11-13-18)16-8-6-15 (7-9-16)14-4-2-1-3-5-14/h1-13H. XNBGHWRYLJOQAU-UHFFFAOYSA-N. 95%+. | |
| 4-Bromopyrene | 4-Bromopyrene. Group: Small molecule semiconductor building blockselectroluminescence materials semiconductor blocks. CAS No. 1732-26-9. Product ID: 4-bromopyrene. Molecular formula: 281.14. Mole weight: C16H9Br. C1=CC2=C3C (=C1)C=C (C4=CC=CC (=C43)C=C2)Br. InChI=1S / C16H9Br / c17-14-9-12-5-1-3-10-7-8-11-4-2-6-13 (14) 16 (11) 15 (10) 12 / h1-9H. QMHTZTOPYZKQLC-UHFFFAOYSA-N. 97%. | |
| 4-Bromothiophene-3-carboxaldehyde | 4-Bromothiophene-3-carboxaldehyde. Group: Small molecule semiconductor building blockssemiconductor blocks. CAS No. 18791-78-1. Product ID: 4-bromothiophene-3-carbaldehyde. Molecular formula: 191.05g/mol. Mole weight: C5H3BrOS. C1=C(C(=CS1)Br)C=O. InChI=1S/C5H3BrOS/c6-5-3-8-2-4 (5)1-7/h1-3H. ZDVHJQOCVBTMOF-UHFFFAOYSA-N. | |
| 4'-Bromotri(4-biphenylyl)amine | 4'-Bromotri(4-biphenylyl)amine. Group: Small molecule semiconductor building blockssemiconductor blocks. CAS No. 728039-63-2. Product ID: N-[4-(4-bromophenyl)phenyl]-4-phenyl-N-(4-phenylphenyl)aniline. Molecular formula: 552.5g/mol. Mole weight: C36H26BrN. C1=CC=C (C=C1)C2=CC=C (C=C2)N (C3=CC=C (C=C3)C4=CC=CC=C4)C5=CC=C (C=C5)C6=CC=C (C=C6)Br. InChI=1S/C36H26BrN/c37-33-19-11-29 (12-20-33) 32-17-25-36 (26-18-32) 38 (34-21-13-30 (14-22-34) 27-7-3-1-4-8-27) 35-23-15-31 (16-24-35) 28-9-5-2-6-10-28/h1-26H. VBQIVFTUXFKGKW-UHFFFAOYSA-N. | |
| 4-Butoxy-4'-cyanobiphenyl | 4-Butoxy-4'-cyanobiphenyl. Group: Liquid crystal (lc) materials. Alternative Names: 4'-Butyloxy-4-biphenylcarbonitrile 4OCB. CAS No. 52709-87-2. Product ID: 4-(4-butoxyphenyl)benzonitrile. Molecular formula: 251.33. Mole weight: C17H17NO. CCCCOC1=CC=C(C=C1)C2=CC=C(C=C2)C#N. InChI=1S / C17H17NO / c1-2-3-12-19-17-10-8-16 (9-11-17) 15-6-4-14 (13-18) 5-7-15 / h4-11H, 2-3, 12H2, 1H3. KPQVQWUNELODQE-UHFFFAOYSA-N. >98.0%(GC). | |
| 4-Butoxybenzoic Acid | 4-Butoxybenzoic Acid. Group: Liquid crystal (lc) building blocksliquid crystal (lc) materials. Alternative Names: p -(Butyloxy)benzoic acid,p -Butoxybenzoic acid. CAS No. 1498-96-0. Product ID: 4-butoxybenzoic acid. Molecular formula: 194.23. Mole weight: C11H14O3. CCCCOC1=CC=C(C=C1)C(=O)O. InChI=1S / C11H14O3 / c1-2-3-8-14-10-6-4-9 (5-7-10) 11 (12) 13 / h4-7H, 2-3, 8H2, 1H3, (H, 12, 13). LAUFPZPAKULAGB-UHFFFAOYSA-N. >98.0%(GC)(T). | |
| 4'-Butoxybenzylidene-4-cyanoaniline | 4'-Butoxybenzylidene-4-cyanoaniline. Group: Liquid crystal (lc) building blocksliquid crystal (lc) materials. Alternative Names: 4-(4-Butoxybenzylideneamino)benzonitrile. CAS No. 36405-17-1. Product ID: 4-[ (4-butoxyphenyl) methylideneamino]benzonitrile. Molecular formula: 278.36. Mole weight: C18H18N2O. CCCCOC1=CC=C (C=C1)C=NC2=CC=C (C=C2)C#N. InChI=1S / C18H18N2O / c1-2-3-12-21-18-10-6-16 (7-11-18) 14-20-17-8-4-15 (13-19) 5-9-17 / h4-11, 14H, 2-3, 12H2, 1H3. JWLPZJPDDBBWQD-UHFFFAOYSA-N. 98%+. | |
| 4-Butoxyphenyl 4-Pentylbenzoate | 4-Butoxyphenyl 4-Pentylbenzoate. Group: Liquid crystal (lc) building blocksliquid crystal (lc) materials. Alternative Names: 4-Amylbenzoic Acid 4-Butoxyphenyl Ester. CAS No. 51128-24-6. Product ID: (4-butoxyphenyl) 4-pentylbenzoate. Molecular formula: 340.46. Mole weight: C22H28O3. CCCCCC1=CC=C (C=C1)C (=O)OC2=CC=C (C=C2)OCCCC. InChI=1S / C22H28O3 / c1-3-5-7-8-18-9-11-19 (12-10-18) 22 (23) 25-21-15-13-20 (14-16-21) 24-17-6-4-2 / h9-16H, 3-8, 17H2, 1-2H3. LEJYVZMFIRFBCQ-UHFFFAOYSA-N. 99%+. | |
| 4-Butoxyphenylboronic Acid (contains varying amounts of Anhydride) | 4-Butoxyphenylboronic Acid (contains varying amounts of Anhydride). Group: Liquid crystal (lc) building blocks. Alternative Names: 4-Butoxybenzeneboronic Acid (contains varying amounts of Anhydride). CAS No. 105365-51-3. Product ID: (4-butoxyphenyl)boronic acid. Molecular formula: 194.04. Mole weight: C10H15BO3. B(C1=CC=C(C=C1)OCCCC)(O)O. InChI=1S / C10H15BO3 / c1-2-3-8-14-10-6-4-9 (5-7-10) 11 (12) 13 / h4-7, 12-13H, 2-3, 8H2, 1H3. QUPFQMXWFNJUNJ-UHFFFAOYSA-N. | |
| 4-Butoxyphthalonitrile | 4-Butoxyphthalonitrile. Group: Phthalonitriles & naphthalonitrilesphthalocyanine building blocks. CAS No. 81560-32-9. Product ID: 4-butoxybenzene-1,2-dicarbonitrile. Molecular formula: 200.24g/mol. Mole weight: C12H12N2O. CCCCOC1=CC(=C(C=C1)C#N)C#N. InChI=1S / C12H12N2O / c1-2-3-6-15-12-5-4-10 (8-13) 11 (7-12) 9-14 / h4-5, 7H, 2-3, 6H2, 1H3. AVGCGXBXMPWLOW-UHFFFAOYSA-N. | |
| 4-Butyl-4'-cyanobiphenyl | 4-Butyl-4'-cyanobiphenyl. Group: Liquid crystal (lc) materials. Alternative Names: 4'-Butyl-4-biphenylcarbonitrile 4CB. CAS No. 52709-83-8. Product ID: 4-(4-butylphenyl)benzonitrile. Molecular formula: 235.33. Mole weight: C17H17N. CCCCC1=CC=C(C=C1)C2=CC=C(C=C2)C#N. InChI=1S/C17H17N/c1-2-3-4-14-5-9-16 (10-6-14)17-11-7-15 (13-18)8-12-17/h5-12H, 2-4H2, 1H3. PJPLBHHDTUICNN-UHFFFAOYSA-N. >98.0%(GC). | |
| 4-Butylacetophenone | 4-Butylacetophenone. Group: Liquid crystal (lc) building blocks. CAS No. 37920-25-5. Product ID: 1-(4-butylphenyl)ethanone. Molecular formula: 176.25g/mol. Mole weight: C12H16O. CCCCC1=CC=C(C=C1)C(=O)C. InChI=1S/C12H16O/c1-3-4-5-11-6-8-12 (9-7-11)10 (2)13/h6-9H, 3-5H2, 1-2H3. MQESVSITPLILCO-UHFFFAOYSA-N. | |
| 4'-Butylacetophenone | 4'-Butylacetophenone. Group: Liquid crystal (lc) building blocks. CAS No. 37920-25-5. Product ID: 1-(4-butylphenyl)ethanone. Molecular formula: 176.26. Mole weight: C12H16O. CCCCC1=CC=C(C=C1)C(=O)C. InChI=1S/C12H16O/c1-3-4-5-11-6-8-12 (9-7-11)10 (2)13/h6-9H, 3-5H2, 1-2H3. MQESVSITPLILCO-UHFFFAOYSA-N. >97.0%(GC). | |
| 4-Butylbenzoyl Chloride | 4-Butylbenzoyl Chloride. Group: Liquid crystal (lc) building blocksliquid crystal (lc) materials. CAS No. 28788-62-7. Product ID: 4-butylbenzoyl chloride. Molecular formula: 196.67. Mole weight: C11H13CIO. CCCCC1=CC=C(C=C1)C(=O)Cl. InChI=1S/C11H13ClO/c1-2-3-4-9-5-7-10 (8-6-9)11 (12)13/h5-8H, 2-4H2, 1H3. OUOWCSJYDCPVDM-UHFFFAOYSA-N. >96.0%(GC)(T). | |
| 4-Butylcyclohexanecarboxylic Acid (cis- and trans- mixture) | 4-Butylcyclohexanecarboxylic Acid (cis- and trans- mixture). Group: Liquid crystal (lc) building blocks. CAS No. 71101-89-8. Product ID: 4-butylcyclohexane-1-carboxylic acid. Molecular formula: 184.28. Mole weight: C11H20O2. CCCCC1CCC(CC1)C(=O)O. InChI=1S/C11H20O2/c1-2-3-4-9-5-7-10 (8-6-9)11 (12)13/h9-10H, 2-8H2, 1H3, (H, 12, 13). BALGERHMIXFENA-UHFFFAOYSA-N. >98.0%(GC)(T). | |
| 4-Butylcyclohexanecarboxylic Acid, (cis- and trans- mixture) | 4-Butylcyclohexanecarboxylic Acid, (cis- and trans- mixture). Group: Liquid crystal (lc) building blocks. CAS No. 71101-89-8. Product ID: 4-butylcyclohexane-1-carboxylic acid. Molecular formula: 184.27g/mol. Mole weight: C11H20O2. CCCCC1CCC(CC1)C(=O)O. InChI=1S/C11H20O2/c1-2-3-4-9-5-7-10 (8-6-9)11 (12)13/h9-10H, 2-8H2, 1H3, (H, 12, 13). BALGERHMIXFENA-UHFFFAOYSA-N. | |
| 4-Butylphenylboronic Acid (contains varying amounts of Anhydride) | 4-Butylphenylboronic Acid (contains varying amounts of Anhydride). Group: Liquid crystal (lc) building blocks. Alternative Names: 4-Butylbenzeneboronic Acid (contains varying amounts of Anhydride). CAS No. 145240-28-4. Product ID: (4-butylphenyl)boronic acid. Molecular formula: 178.04. Mole weight: C10H15BO2. B(C1=CC=C(C=C1)CCCC)(O)O. InChI=1S/C10H15BO2/c1-2-3-4-9-5-7-10 (8-6-9)11 (12)13/h5-8, 12-13H, 2-4H2, 1H3. UGZUUTHZEATQAM-UHFFFAOYSA-N. | |
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