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Standard building block of introduction of D-cyclohexyl amino-acid residues by Fmoc SPPS. Uses: Peptide synthesis. Additional or Alternative Names: Fmoc-D-Cha-OH, N-α-Fmoc-β-cyclohexyl-D-alanine. Product Category: Amino Acids. CAS No. 144701-25-7. Mole weight: 393.48. Product ID: ACM144701257. Alfa Chemistry ISO 9001:2015 Certified. Categories: (R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-cyclohexylpropanoic acid.
Fmoc-D-citrulline
Fmoc-D-citrulline. Group: Biochemicals. Alternative Names: Fmoc-D-Cit-OH; (R)-2-Fmoc-amino-5-ureidopentanoic acid; Fmoc-D-Orn(carbamoyl)-OH. Grades: Highly Purified. CAS No. 200344-33-8. Pack Sizes: 500mg, 1g, 2g, 5g. US Biological Life Sciences.
Fmoc-D-cyclopentylglycine 99+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 250mg, 1g, 5g. US Biological Life Sciences.
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Fmoc-D-cyclopropylglycine
Fmoc-D-cyclopropylglycine. Group: Biochemicals. Alternative Names: Fmoc-(R)-amino-cyclopropyl-acetic acid. Grades: Highly Purified. CAS No. 923012-40-2. Pack Sizes: 100mg, 250mg, 500mg, 1g, 2g. US Biological Life Sciences.
Worldwide
Fmoc-D-cyclopropylglycine 99+%
Fmoc-D-cyclopropylglycine 99+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100mg, 250mg, 1g, 5g. US Biological Life Sciences.
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Fmoc-D-Cys(tBu)-OH
Fmoc-D-Cys(tBu)-OH. Group: Biochemicals. Alternative Names: Fmoc-S-tert-butyl-D-cysteine. Grades: Highly Purified. CAS No. 131766-22-8. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C22H25NO4S. US Biological Life Sciences.
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Fmoc-D-cysteine
Fmoc-D-cysteine is an N-Fmoc-protected form of D-Cysteine. D-Cysteine is a strong inhibitor of Escherichia coli growth and also functions to provide inorganic sulfates for the sulfation of xenobiotics. D-Cysteine is a non-physiological isomer of L-Cysteine, and is not involved in protein or glutathione synthesis. Synonyms: N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-cysteine; Fmoc-L-Cys-OH; Fmoc-cysteine; N-(9-Fluorenylmethoxycarbonyl)cysteine. Grades: 96%. CAS No. 157355-80-1. Molecular formula: C18H17NO4S. Mole weight: 343.40.
Fmoc-D-Cysteine hydrate
Fmoc-D-Cysteine hydrate. Group: Biochemicals. Grades: Highly Purified. CAS No. 157355-80-1. Pack Sizes: 25mg, 50mg, 100mg, 250mg, 500mg. Molecular Formula: C18H17NO4S. US Biological Life Sciences.
Worldwide
Fmoc-D-cysteine hydrate 98+% (HPLC)
Fmoc-D-cysteine hydrate 98+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100mg, 250mg, 1g, 5g. US Biological Life Sciences.
Worldwide
Fmoc-D-Cys(Trt)-OH
Fmoc-D-Cys(Trt)-OH is a cysteine derivative [1]. Uses: Scientific research. Group: Peptides. CAS No. 167015-11-4. Pack Sizes: 25 g; 100 g. Product ID: HY-W010724.
Fmoc-D-Cys(Trt)-OH
Standard building block of introduction of D-cysteine amino-acid residues by Fmoc SPPS. Uses: Peptide synthesis. Additional or Alternative Names: Nα-Fmoc-S-trityl-D-cysteine. Product Category: Amino Acids. CAS No. 167015-11-4. Molecular formula: C37H31NO4S. Mole weight: 585.71. Canonical SMILES: OC(=O)[C@@H](CSC(c1ccccc1)(c2ccccc2)c3ccccc3)NC(=O)OCC4c5ccccc5-c6ccccc46. Product ID: ACM167015114. Alfa Chemistry ISO 9001:2015 Certified.
Fmoc-D-Dab(Boc)-OH is an amino acid derivative with an Fmoc protecting group, which can be used to synthesize peptides with antibacterial activity [1]. Uses: Scientific research. Group: Peptides. CAS No. 114360-56-4. Pack Sizes: 1 g; 5 g; 10 g; 25 g. Product ID: HY-W019032.
Fmoc-D-Dap(Boc)-OH is an amino acid derivative with an Fmoc protecting group, which can be used to synthesize bioactive peptide mimetics, such as DOTA-modified peptides and their metal chelates with cancer diagnostic effects [1]. Uses: Scientific research. Group: Peptides. CAS No. 198544-42-2. Pack Sizes: 1 g; 5 g; 10 g; 25 g; 50 g; 100 g. Product ID: HY-W046355.
Fmoc-D-Dbu(Boc)-OH. Group: Biochemicals. Alternative Names: (S)-Nb-Fmoc-Nγ-Boc-3,4-diaminobutyric acid. Grades: Highly Purified. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. US Biological Life Sciences.
Worldwide
Fmoc-D-Dbu(Boc)-OH ≥97% (HPLC)
Fmoc-D-Dbu(Boc)-OH ≥97% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100mg, 250mg, 1g. US Biological Life Sciences.
Worldwide
Fmoc-D-Dpr(ivDde)-OH
This orthogonally-protected derivative is based on the hindered Dde variant ivDde. It has very similar chemical properties to Fmoc-Lys(Dde)-OH, except that the side-chain ivDde group is considerably more stable to piperidine than Dde, and is less prone to migrate from protected to unprotected lysine side-chains. 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. Guide to Selection of Orthogonally-Protected Building Blocks for Fmoc SPPS. Uses: Peptide synthesis. Additional or Alternative Names: Fmoc-D-Dpr(ivDde)-OH, N-α-Fmoc-N-β-1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl-D-diaminopropionic acid. Product Category: Amino Acids. CAS No. 1228900-15-9. Mole weight: 532.63. Product ID: ACM1228900159-1. Alfa Chemistry ISO 9001:2015 Certified.
Fmoc-δ-azidonorvaline
A useful tool for the synthesis of branched, side-chain modified, cyclic peptides and peptide tools for click chemistry by Fmoc SPPS. The side-chain azido group is completely stable to piperidine and TFA, but can be readily converted to an amine on the solid phase or in solution by reduction with thiols or phosphines. Guide to Selection of Orthogonally-Protected Building Blocks for Fmoc SPPS Literature references M. Meldal, et al. (1997) Tetrahedron Lett., 38, 2531. J. T. Lundquist & J. C. Pelletier (2001) Org. Lett., 3, 781. N. Nepomniaschiy, et al. (2008) Org. Lett., 10, 5243. Uses: Peptide synthesis. Additional or Alternative Names: Fmoc-δ-azidonorvaline, (2S)-N-Fmoc-5-azido-pentanoic acid. Product Category: Amino Acids. CAS No. 1097192-04-5. Molecular formula: C20H20N4O4. Mole weight: 380.4. Product ID: ACM1097192045-1. Alfa Chemistry ISO 9001:2015 Certified.
Fmoc-D-Gln-OH
Standard building block of introduction of D-glutamine amino-acid residues by Fmoc SPPS. Uses: Peptide synthesis. Additional or Alternative Names: Fmoc-D-Gln-OH, N-α-Fmoc-D-glutamine. Product Category: Amino Acids. CAS No. 112898-00-7. Mole weight: 368.38. Product ID: ACM112898007-1. Alfa Chemistry ISO 9001:2015 Certified.
Fmoc-D-Gln(Trt)-OH is a glutamine derivative [1]. Uses: Scientific research. Group: Peptides. CAS No. 200623-62-7. Pack Sizes: 1 g; 5 g; 10 g. Product ID: HY-W010714.
Fmoc-D-Gln(Trt)-OH
Standard building block of introduction of D-glutamine amino-acid residues by Fmoc SPPS. Uses: Peptide synthesis. Additional or Alternative Names: Fmoc-N-trityl-D-glutamine. Product Category: Amino Acids. CAS No. 200623-62-7. Molecular formula: C39H34N2O5. Mole weight: 610.7. Canonical SMILES: OC(=O)[C@@H](CCC(=O)NC(c1ccccc1)(c2ccccc2)c3ccccc3)NC(=O)OCC4c5ccccc5-c6ccccc46. Product ID: ACM200623627. Alfa Chemistry ISO 9001:2015 Certified. Categories: N-Fmoc-N'-trityl-D-glutamine.
Fmoc-D-Glu-ODmab
Fmoc-D-Glu-ODmab is a glycine-extended peptide that is used as a resin-bound peptide for solid-phase peptide synthesis. The D-glutamic acid residue has a higher chemical stability compared to L-glutamic acid, which makes it a suitable component for peptide synthesis. The Fmoc group serves as a protecting group for the amino group, which is removed during the peptide elongation process. The ODmab group serves as a C-terminal protecting group that can be removed using mild acidic conditions. Uses: Peptide synthesis. Additional or Alternative Names: Fmoc-D-Glu-ODmab, N-α-Fmoc-D-glutamic acid α-4-{N-[1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl]-amino} benzyl ester. Product Category: Amino Acids. CAS No. 874486-65-4. Molecular formula: C40H44N2O8. Mole weight: 680.79. IUPACName: (4R)-4-(9H-fluoren-9-ylmethoxycarbonylamino)-5-[[4-[[1-(2-hydroxy-4,4-dimethyl-6-oxocyclohexen-1-yl)-3-methylbutylidene]amino]phenyl]methoxy]-5-oxopentanoic acid. Canonical SMILES: CC(C)CC(=NC1=CC=C(C=C1)COC(=O)C(CCC(=O)O)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24)C5=C(CC(CC5=O)(C)C)O. Product ID: ACM874486654. Alfa Chemistry ISO 9001:2015 Certified.
Fmoc-D-Glu-OH
N-Fmoc-D-glutamic acid is an N-Fmoc-protected form of D-Glutamic acid. D-Glutamic Acid is the unnatural (R)-enantiomer of Glutamic Acid, a non-essential amino acid. Its salt form (glutamate) is an important neurotransmitter that plays a key role in long-term potentiation and is important for learning and memory. Glutamic Acid is also a key molecule in cellular metabolism. Synonyms: N-[(9H-Fluoren-9-ylMethoxy)carbonyl]-D-glutaMic Acid; Fmoc-D-Glu-OH; N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-glutamic Acid; N-Fmoc-D-glutamic Acid; (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)pentanedioic acid. Grades: ≥ 95%. CAS No. 104091-09-0. Molecular formula: C20H19NO6. Mole weight: 369.38.
Fmoc-D-glutamine 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g, 100g. US Biological Life Sciences.
Worldwide
Fmoc-Dha-OH
Fmoc-Dha-OH, a pivotal intermediate, is used for synthesizing a plethora of biologically active compounds encompassing antimicrobial peptides, dipeptidyl peptidase IV inhibitors, and enzyme inhibitors. Researchers have employed it to fabricate Fmoc-Dha-OH-derived peptidomimetics manifested by the impeding activity against a myriad of cancer cell lines. The said compound holds sheer potential for the design and development of novel pharmaceutical agents targeting numerous diseases. Synonyms: Fmoc-dehydro-Ala-OH; N-(9H-Fluorene-9-ylmethoxycarbonyl)-2,3-didehydro-L-alanine; 2-(((9H-fluoren-9-yl)methoxy)carbonylamino)acrylic acid. CAS No. 261522-33-2. Molecular formula: C18H15NO4. Mole weight: 309.3.
Fmoc-Dha-OH
Fmoc-Dha-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Signaling pathways. CAS No. 261522-33-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W348896.
Building block for introduction of D-histidine by Fmoc SPPS. The Clt group is more stable to acid than Trt and its use avoids the formation of partially protected histidine peptides during the preparation of protected fragments. Uses: Peptide synthesis. Additional or Alternative Names: Fmoc-D-His(Clt)-OH, N-α-Fmoc-N-im-2-chlorotrityl-D-histidine. Product Category: Amino Acids. CAS No. 1272755-56-2. Molecular formula: C40H32ClN3O4. Mole weight: 654.15. IUPACName: (2R)-3-[1-[(2-chlorophenyl)-diphenylmethyl]imidazol-4-yl]-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoic acid. Canonical SMILES: C1=CC=C(C=C1)C(C2=CC=CC=C2)(C3=CC=CC=C3Cl)N4C=C(N=C4)CC(C(=O)O)NC(=O)OCC5C6=CC=CC=C6C7=CC=CC=C57. Product ID: ACM1272755562. Alfa Chemistry ISO 9001:2015 Certified.
Fmoc-D-his(fmoc)-oh
Fmoc-D-his(fmoc)-oh. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Fmoc-D-His(Fmoc)-OH, AKOS015950652, AK131099, AB1002870, 200926-18-7. Product Category: Heterocyclic Organic Compound. CAS No. 200926-18-7. Molecular formula: C36H29N3O6. Mole weight: 599.64. Purity: 0.96. IUPACName: (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-[1-(9H-fluoren-9-ylmethoxycarbonyl)imidazol-4-yl]propanoic acid. Canonical SMILES: C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NC(CC4=CN(C=N4)C(=O)OCC5C6=CC=CC=C6C7=CC=CC=C57)C(=O)O. Product ID: ACM200926187. Alfa Chemistry ISO 9001:2015 Certified.
Fmoc-D-His(Trt)-OH
Standard building block of introduction of D-histidine amino-acid residues by Fmoc SPPS. Uses: Peptide synthesis. Additional or Alternative Names: Fmoc-N(im)-trityl-D-histidine. Product Category: Amino Acids. CAS No. 135610-90-1. Molecular formula: C40H33N3O4. Mole weight: 619.71. Canonical SMILES: OC(=O)[C@@H](Cc1cn(cn1)C(c2ccccc2)(c3ccccc3)c4ccccc4)NC(=O)OCC5c6ccccc6-c7ccccc57. Product ID: ACM135610901. Alfa Chemistry ISO 9001:2015 Certified. Categories: (2R)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-[1-(triphenylmethyl)-1H-imidazol-4-yl]propanoic acid.