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| Product | Description | |
|---|---|---|
| FMOC NH2-PEG3500-NH2TFA | 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). |  |
| Fmoc-NH-3,3-difluorocyclobutane-COOH | Synonyms: 1-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3,3-difluorocyclobutanecarboxylic acid. CAS No. 1936532-04-5. Molecular formula: C20H17F2NO4. Mole weight: 373.3. |  |
| Fmoc-NH-4,4-difluorocyclohexane-COOH | Synonyms: 1-(((9H-fluoren-9-yl)methoxy)carbonylamino)-4,4-difluorocyclohexanecarboxylic acid. CAS No. 1986905-26-3. Molecular formula: C22H21F2NO4. Mole weight: 401.4. | |
| Fmoc-NH-BCP-COOH | Synonyms: 3- ( (9-fluorenylmethoxy) carbonylamino) bicyclo[1. 1. 1]pentane-1-carboxylic acid. CAS No. 676371-66-7. Molecular formula: C21H19NO4. Mole weight: 349.4. | |
| Fmoc-NH-cis-2-Me-cyclohexane-COOH | Synonyms: (1S,2R/1R,2S)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-2-methylcyclohexanecarboxylic acid. Molecular formula: C23H25NO4. Mole weight: 379.4. | |
| Fmoc-NH-cis-2-Me-cyclopentane-COOH | Synonyms: (1S,2R/1R,2S)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-2-methylcyclopentanecarboxylic acid. Molecular formula: C22H23NO4. Mole weight: 365.4. | |
| Fmoc-NH-cis-BCheptane-COOH | Synonyms: (1S, 2R, 3S, 4R/1R, 2S, 3R, 4S)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}bicyclo[2. 2. 1]heptane-2-carboxylic acid; Fmoc-3-exo-aminobicyclo[2.2.1]-heptane-2-exo-carboxylic acid; 3-(9H-fluoren-9-ylmethoxycarbonylamino)bicyclo[2. 2. 1]heptane-2-carboxylic acid. Grades: ≥ 99% (HPLC). CAS No. 352707-75-6. Molecular formula: C23H23NO4. Mole weight: 377.43. | |
| Fmoc-NH-cis-BCheptene-COOH | Synonyms: (1S, 2S, 3R, 4R/1R, 2R, 3S, 4S)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}bicyclo[2. 2. 1]hept-5-ene-2-carboxylic acid. CAS No. 1217848-39-9. Molecular formula: C23H21NO4. Mole weight: 375.4. | |
| Fmoc-NH-cis-cycloheptane-COOH | Synonyms: (1S, 2R / 1R, 2S) -2-{ [ (9H-fluoren-9-ylmethoxy) carbonyl] amino}cycloheptanecarboxylic acid. Molecular formula: C23H25NO4. Mole weight: 379.4. | |
| Fmoc-NH-cis-cyclooct-3-ene-1-COOH | Synonyms: (1S,2R,3Z/1R,2S,3Z)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}cyclooct-3-ene-1-carboxylic acid. Molecular formula: C24H25NO4. Mole weight: 391.5. | |
| Fmoc-NH-cis-cyclooct-4-ene-COOH | Synonyms: (1S,4Z,8R/1R,4Z,8S)-8-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}cyclooct-4-ene-1-carboxylic acid. Molecular formula: C24H25NO4. Mole weight: 391.5. | |
| Fmoc-NH-cis-cyclooctane-COOH | Synonyms: (1S,2R/1R,2S)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}cyclooctane-1-carboxylic acid. Molecular formula: C24H27NO4. Mole weight: 393.5. | |
| Fmoc-NH-cis-cyclopent-3-ene-COOH | Synonyms: (1R,2S/1S,2R)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}cyclopent-3-ene-1-carboxylic acid. Molecular formula: C21H19NO4. Mole weight: 349.4. | |
| Fmoc-NH-cis-cyclopentane-COOH | Synonyms: (1S, 2R / 1R, 2S) -2-{ [ (9H-fluoren-9-ylmethoxy) carbonyl] amino}cyclopentanecarboxylic acid; (1R,2S)-Fmoc-2-amino-1-cyclopentanecarboxylic acid; cis-2-Aminocyclopentanecarboxylic acid,N-FMOC protected; CIS-2- (9-FLUORENYLMETHOXYCARBONYLAMINO) CYCLOPENTANECARBOXYLIC ACID; (+/-)-Fmoc-cis-2-aminocyclopentane carboxylic acid; Fmoc-cis-Acpc; Fmoc-cis-2-aminocyclopentane carboxylic acid. Grades: ≥ 98% (HPLC). CAS No. 352707-76-7. Molecular formula: C21H21NO4. Mole weight: 351.41. | |
| Fmoc-nh-dpeg(4)-cooh | Fmoc-nh-dpeg(4)-cooh. Group: Biochemicals. Grades: Highly Purified. CAS No. 557756-85-1. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. US Biological Life Sciences. |  Worldwide |
| Fmoc-NH-hex-5-enal | Synonyms: 9H-fluoren-9-ylmethyl (1-oxohex-5-en-3-yl)carbamate; N-Fmoc-(+/-)-3-aminohex-5-enal. Molecular formula: C21H21NO3. Mole weight: 335.4. | |
| Fmoc-NH-OH | Synonyms: 9H-fluoren-9-ylmethyl N-hydroxycarbamate; N- (9-Fluorenylmethoxycarbonyl) hydroxylamine; (9H-fluoren-9-yl)methyl N-hydroxycarbamate; (9H-fluoren-9-yl)methyl hydroxycarbamate; 9-Fluorenylmethyl N-hydroxycarbamate. Grades: 98%. CAS No. 190656-01-0. Molecular formula: C15H13NO3. Mole weight: 255.27. | |
| Fmoc-NH-(PEG)10-CH2CH2COOH | Fmoc-NH-PEG10-CH2CH2COOH is a derivative of polyethylene glycol (PEG) that has been modified with a terminal carboxylic acid group and a base-labile 9-Fluorenylmethoxycarbonyl (Fmoc) protecting group. PEG is a biocompatible and highly hydrophilic polymer that is widely used in various biomedical applications due to its excellent solubility, low toxicity, and resistance to protein binding. The addition of a carboxylic acid group to PEG improves its water solubility and allows for conjugation to amino-containing molecules, such as peptides or proteins. The Fmoc protecting group is widely used in solid-phase peptide synthesis to protect the N-terminal amine group of amino acids from undesired side reactions during chain assembly. Uses: Fmoc-nh-peg10-ch2ch2cooh has a wide range of applications in scientific experiments, including drug delivery, diagnostics, and imaging. its hydrophilic and biocompatible nature makes it an ideal polymer for the synthesis of nanoparticles or micelles that can carry hydrophobic drugs and improve their solubility and bioavailability in biological systems. its carboxylic acid group can also be used fo. Additional or Alternative Names: 1-(9H-Fluoren-9-yl)-3-oxo-2,7,10,13,16,19,22,25,28,31,34-undecaoxa-4-azaheptatriacontan-37-oic acid. Product Category: Amino Acids. CAS No. 2101563-45-3. Molecular formula: C38H57NO14. Mole weight: 751.8. Purity: Peak Area by HPLC ≥95%. IUPACName: 3-[2- |  |
| Fmoc-NH-(PEG)12-CH2CH2COOH | Fmoc-NH-(PEG)12-CH2CH2COOH. Uses: Peptide synthesis. Product Category: Amino Acids. CAS No. 756526-01-9. Molecular formula: C42H65NO16. Mole weight: 839.8. Purity: Peak Area by HPLC ≥95%. IUPACName: 3-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(9H-fluoren-9-ylmethoxycarbonylamino)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]propanoic acid. Canonical SMILES: C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCC(=O)O. Product ID: ACM756526019-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-NH-PEG12-CH2CH2COOH | Fmoc-NH-PEG12-CH2CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1952360-91-6. Pack Sizes: 250 mg; 1 g. Product ID: HY-135821. |  |
| Fmoc-NH-PEG3-CH2COOH | Fmoc-NH-PEG3-CH2COOH. Uses: Designed for use in research and industrial production. Product Category: Fmoc PEG Linkers. CAS No. 139338-72-0. Molecular formula: C23H27NO7. Mole weight: 429.46. Purity: 95%+. Product ID: ACM139338720. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-NH-PEG4-CH2COOH | Fmoc-NH-PEG4-CH2COOH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Uses: Designed for use in research and industrial production. Additional or Alternative Names: 5,8,11,14-Tetraoxa-2-azahexadecanedioic acid. Product Category: Fmoc PEG Linkers. Appearance: Liquid. CAS No. 437655-95-3. Molecular formula: C25H31NO8. Mole weight: 473.5. Purity: >90%. IUPACName: 2-[2-[2-[2-[2-(9H-Fluoren-9-ylmethoxycarbonylamino)ethoxy]ethoxy]ethoxy]ethoxy]acetic acid. Canonical SMILES: C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NCCOCCOCCOCCOCC(=O)O. Density: 1.235±0.06 g/cm3. Product ID: ACM437655953. Alfa Chemistry ISO 9001:2015 Certified. | |
| FmocNH-PEG5-acid | FmocNH-PEG5-acid. Uses: Designed for use in research and industrial production. Product Category: Fmoc PEG Linkers. CAS No. 557756-85-1. Molecular formula: C26H33NO8. Mole weight: 487.54. Purity: 95%+. Product ID: ACM557756851. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-NH-PEG5-CH2COOH | Fmoc-NH-PEG5-CH2COOH. Uses: Designed for use in research and industrial production. Product Category: Fmoc PEG Linkers. CAS No. 635287-26-2. Molecular formula: C27H35NO9. Mole weight: 517.23. Purity: 95%+. Product ID: ACM635287262. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-NH-PEG8-CH2COOH | Fmoc-NH-PEG8-CH2COOH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Fmoc-NH-PEG8-CH2COOH is also a PEG-based PROTAC linker that can be used in the synthesis of PROTACs [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 868594-52-9. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-133063. | |
| Fmoc-NH-pent-4-enal | Synonyms: 9H-fluoren-9-ylmethyl (5-oxopent-1-en-3-yl)carbamate; N-Fmoc-(+/-)-3-aminopent-4-enal. CAS No. 1824023-93-9. Molecular formula: C20H19NO3. Mole weight: 321.4. | |
| Fmoc-NH-SAL-PEGA Resin | Synonyms: 4-[ (2, 4-Dimethoxyphenyl) -N- (9-fluorenylmethoxycarbonyl) aminomethyl]phenoxyacetamido polyethyleneglycol polyacrylamide copolymer; N-α-(9-Fluorenylmethoxycarbonyl)-Rinkamide handled bis-2-acrylamidoprop-1-yl polyethyleneglycol crosslinked dimethyl acrylamide and acryloyl sarcosine methyl ester. | |
| Fmoc-NH-SAL-PEG Resin XV | TentaGel resins are grafted copolymers consisting of a low crosslinked polystyrene matrix on which poly(ethylene glycol) (PEG or POE) is grafted. Synonyms: TentaGel XV RAM; 4-[ (2, 4-Dimethoxyphenyl) -N- (9-fluorenylmethoxycarbonyl) aminomethyl]phenoxyacetamido polyethyleneglycol resin. | |
| Fmoc N-hydroxysuccinimide ester | Fmoc N-hydroxysuccinimide ester. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 9-Fluorenylmethyl N-succinimidyl carbonate, N-(9-Fluorenylmethoxycarbonyloxy)succinimide, Fmoc-OSu. Product Category: 9-Fluorenylmethyloxycarbonylation (Fmoc) Reagents. CAS No. 82911-69-1. Molecular formula: C19H15NO5. Mole weight: 337.33. Purity: 0.98. Product ID: ACM82911691-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-N-im-trityl-L-Histidine (Fmoc-L-His(Trt)-OH) | 5g Pack Size. Group: Amino Acids. Formula: C40H33N3O4. CAS No. 109425-51-6. Prepack ID 90028506-5g. Molecular Weight 619.71. See USA prepack pricing. |  |
| Fmoc-N-(isobutyl)glycine | Fmoc-N-(isobutyl)glycine. Group: Biochemicals. Alternative Names: Fmoc-N-(isobutyl)-Gly-OH; Fmoc-Nleu-OH. Grades: Highly Purified. Pack Sizes: 500mg, 1g, 2g, 5g. US Biological Life Sciences. | Worldwide |
| Fmoc-N-(isobutyl)glycine 99+% (HPLC) | Fmoc-N-(isobutyl)glycine 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g. US Biological Life Sciences. | Worldwide |
| Fmoc-N-isobutyl-hydroxylamine | Fmoc-N-isobutyl-hydroxylamine. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Fmoc-Nle-OH | Standard building block for introduction of norleucine amino-acid residues by Fmoc SPPS. Uses: Peptide synthesis. Additional or Alternative Names: Fmoc-Nle-OH, N-α-Fmoc-L-norleucine. Product Category: Amino Acids. CAS No. 77284-32-3. Molecular formula: C21H23NO4. Mole weight: 353.41. Product ID: ACM77284323. Alfa Chemistry ISO 9001:2015 Certified. Categories: (2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)hexanoic acid. | |
| Fmoc-N-Me-3-(4-py)-L-Ala | Fmoc-N-Me-3-(4-py)-L-Ala, a synthetic molecule, finds widespread use in the synthesis of peptides and proteins. Owing to its crucial role as a fundamental building block in solid-phase peptide synthesis, it has emerged as a potent weapon in the battle against numerous human maladies such as cancer and infectious diseases. With versatile functionality and chemical reactivity, the compound facilitates modifications and attachment to the peptide chain, rendering it a prized asset in the biomedical industry and a tool much sought after by researchers. Synonyms: Fmoc-N(Me)4Pal-OH; (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-(pyridin-4-yl)propanoic acid. CAS No. 2381854-90-4. Molecular formula: C24H22N2O4. Mole weight: 402.4. | |
| Fmoc-N-Me-Aib-OH | Synonyms: 2-((((9H-Fluoren-9-Yl)Methoxy)Carbonyl)(Methyl)Amino)-2-Methylpropanoic Acid. CAS No. 400779-65-9. Molecular formula: C20H21NO4. Mole weight: 339.4. | |
| Fmoc-N-Me-Ala-OH | Fmoc-N-Me-Ala-OH can be used for peptide coupling reactions. Synonyms: Fmoc-N-methyl-L-alanine; (S)-2- ( ( ( (9H-Fluoren-9-yl)methoxy)carbonyl) (methyl)amino)propanoic acid; Fmoc-Nalpha-methyl-L-alanine; Fmoc-L-MeAla-OH; Fmoc-N-Methyl-Ala-OH; Fmoc-N-a-methyl-L-alanine. Grades: ≥99% by HPLC. CAS No. 84000-07-7. Molecular formula: C19H19NO4. Mole weight: 325.36. | |
| Fmoc-N-Me-Ala-OH | Building block for introduction of N-α-methyl-alanine amino-acid residues by Fmoc SPPS. Uses: Peptide synthesis. Additional or Alternative Names: Fmoc-N-Me-Ala-OH, N-α-Fmoc-N-α-methyl-L-alanine. Product Category: Amino Acids. CAS No. 84000-07-7. Mole weight: 325.36. Product ID: ACM84000077. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-N-Me-Ala-OH | Fmoc-N-Me-Ala-OH, an N-Fmoc-N-methyl amino acid, is available for the peptide-coupling reaction. Uses: Scientific research. Group: Signaling pathways. CAS No. 84000-07-7. Pack Sizes: 10 mM * 1 mL; 1 g; 5 g. Product ID: HY-W008235. | |
| Fmoc-N-Me-Arg(pbf)-OH | Fmoc-N-Me-Arg(pbf)-OH. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Fmoc-N-Me-Arg(Pbf)-OH. Appearance: White to off-white powder. CAS No. 913733-27-4. Molecular formula: C35H42N4O7S. Mole weight: 662.79. Purity: 0.98. Product ID: ACM913733274. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-N-Me-Arg(Pbf)-OH | Fmoc-N-Me-Arg(Pbf)-OH is an amino acid derivative containing a guanidinium protecting group on the arginine side chain. Fmoc-N-Me-Arg(Pbf)-OH is used in the synthesis of neurotensin-derived NTS1 ligands for PET imaging [1]. Uses: Scientific research. Group: Peptides. CAS No. 913733-27-4. Pack Sizes: 500 mg; 1 g. Product ID: HY-137002. | |
| Fmoc-N-Me-Asn(Trt)-OH | Building block for introduction of N-α-methyl-asparagine amino-acid residues by Fmoc SPPS. Uses: Peptide synthesis. Additional or Alternative Names: Fmoc-N-Me-Asn(Trt)-OH, N-α-Fmoc-N-α-methyl-N-β-trityl-L-asparagine. Product Category: Amino Acids. CAS No. 941296-80-6. Mole weight: 610.7. Product ID: ACM941296806-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-N-Me-Asp(OtBu)-OH | Synonyms: Fmoc-N-methyl-L-aspartic acid β-tert-butyl ester; Fmoc-N-methyl-L-aspartic acid 4-tert-butyl ester; N-Methyl aspartic acid; Fmoc-N-Me-Asp(OtBu)-OH. Grades: ≥ 99.5% (Chiral HPLC). CAS No. 152548-66-8. Molecular formula: C24H27NO6. Mole weight: 425.50. | |
| Fmoc-N-Me-Asp(OtBu)-OH | Building block for introduction of N-α-methyl-aspartic acid amino-acid residues by Fmoc SPPS. Uses: Fmoc protected n-methyl amino acid suitable for solid phase peptide synthesis. n-methyl amino acids have been shown to improve proteolytic stability of peptides. Additional or Alternative Names: N-Methyl aspartic acid, N-α-Fmoc-N-α-methyl-L-aspartic acid β-tert butyl ester. Product Category: Amino Acids. CAS No. 152548-66-8. Mole weight: 425.47. Canonical SMILES: OC([C@@H](N(C(OCC1C2=C(C=CC=C2)C3=C1C=CC=C3)=O)C)CC(OC(C)(C)C)=O)=O. Product ID: ACM152548668-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-N-Me-Asp(OtBu)-OH | Fmoc protected N-methyl amino acid suitable for solid phase peptide synthesis. N-methyl amino acids have been shown to improve proteolytic stability of peptides. Group: Biochemicals. Alternative Names: N-α-Fmoc-N-α-methyl-L-aspartic acid β-tert butyl ester. Grades: Purified. CAS No. 152548-66-8. Pack Sizes: 250mg, 1g. US Biological Life Sciences. | Worldwide |
| Fmoc-N-Me-Asp(OtBu)-OH | Fmoc-N-Me-Asp(OtBu)-OH is an aspartic acid derivative [1]. Uses: Scientific research. Group: Peptides. CAS No. 152548-66-8. Pack Sizes: 500 mg; 1 g; 5 g. Product ID: HY-W013740. | |
| Fmoc-N-Me-Cys(Trt)-OH | Molecular Weight: Group: Biochemicals. Grades: Highly Purified. CAS No. 944797-51-7. Pack Sizes: 250mg, 1g. US Biological Life Sciences. | Worldwide |
| Fmoc-N-Me-Cys(Trt)-OH | Building block for introduction of N-α-methyl-cysteine amino-acid residues by Fmoc SPPS. Fmoc SPPS of Cysteine-Containing Peptides. Uses: Fmoc-n-me-cys(trt)-oh is a fmoc-protected derivative of n-methyl cysteine used as a building block to prepare peptide thioesters under acidic conditions. the residue attached to the amino group of n-methylcysteine can migrate to the cysteinyl thiol group, resulting in the formation of a peptide thioester. the introduction of this fmoc-protected derivative is best achieved using hatu as a coupling reagent in the presence of dipea (n, n-diisopropylethylamine). it can also be used to prepare fmoc-n-me-cys(trt)-oallyl intermediate for the solid-phase synthesis of dithiol triostin a. Additional or Alternative Names: N-α-Fmoc-N-α-methyl-S-trityl-L-cysteine. Product Category: Amino Acids. CAS No. 944797-51-7. Mole weight: 599.74. Product ID: ACM944797517. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-N-Me-Dab(Boc)-OH | Fmoc-N-Me-Dab(Boc)-OH, a peptide derivative, finds extensive applications in the pharmaceutical and biologically active compound synthesis arena. One can leverage it as a fundamental building block to engineer peptide-based drugs with proven anti-tumor activity. The versatility of Fmoc-N-Me-Dab(Boc)-OH renders it an indispensable tool in the scientific community, and its intricate molecular structure continues to inspire novel applications in the field of drug discovery and development. Synonyms: (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-4-((tert-butoxycarbonyl)amino)butanoic acid. CAS No. 2044702-38-5. Molecular formula: C25H30N2O6. Mole weight: 454.5. | |
| Fmoc-N-Me-D-Ala(2-naphthyl)-OH | Fmoc-N-Me-D-Ala(2-naphthyl)-OH. Group: Biochemicals. Grades: Reagent Grade. CAS No. 179385-30-9. Pack Sizes: 250mg, 1g, 5g. US Biological Life Sciences. | Worldwide |
| Fmoc-N-Me-Dap(Boc)-OH | Molecular formula: C25H30N2O6. Mole weight: 454.52. | |
| Fmoc-N-Me-D-Cys(Trt)-OH | Fmoc-N-Me-D-Cys(Trt)-OH. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. US Biological Life Sciences. | Worldwide |
| Fmoc-N-Me-D-Leu-OH | Fmoc-N-Me-D-Leu-OH. Uses: Peptide synthesis. Additional or Alternative Names: Fmoc-N-methyl-D-leucine. Product Category: Amino Acids. CAS No. 103478-63-3. Mole weight: 367.44. Canonical SMILES: CC(C)C[C@@H](N(C)C(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O. Product ID: ACM103478633-1. Alfa Chemistry ISO 9001:2015 Certified. Categories: N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N-methyl-D-leucine. | |
| Fmoc-N-Me-D-Lys(Boc)-OH | Fmoc-N-Me-D-Lys(Boc)-OH is a multifaceted chemical agent that is employed in the synthetic production of proteins and peptides. This chemical is highly valued in the medical industry for its efficacy in treating infectious diseases and cancers. Scientists have also harnessed its potential for biochemical research pertaining to the design of pharmaceuticals directed towards targeted proteins. Synonyms: Fmoc-D-N(Me)Lys(Boc)-OH. CAS No. 1793105-27-7. Molecular formula: C27H34N2O6. Mole weight: 482.6. | |
| Fmoc-N-Me-D-Phe-OH | Fmoc-N-Me-D-Phe-OH. Uses: Peptide synthesis. Additional or Alternative Names: Fmoc-N-methyl-D-phenylalanine. Product Category: Amino Acids. CAS No. 138775-05-0. Mole weight: 401.45. Canonical SMILES: CN([C@H](Cc1ccccc1)C(O)=O)C(=O)OCC2c3ccccc3-c4ccccc24. Product ID: ACM138775050-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-N-Me-D-Trp(Boc)-OH | Synonyms: Fmoc-DL-N(Me)Trp(Boc)-OH. CAS No. 2044709-90-0. Molecular formula: C32H32N2O6. Mole weight: 540.6. | |
| Fmoc-N-Me-Glu(OtBu)-OH | Building block for introduction of N-α-methyl-glutamic acid amino-acid residues by Fmoc SPPS. Uses: Peptide synthesis. Additional or Alternative Names: Fmoc-N-Me-Glu(OtBu)-OH, N-α-Fmoc-N-α-methyl-Lglutamic acid γ-tert butyl ester. Product Category: Amino Acids. CAS No. 200616-40-6. Mole weight: 439.5. Product ID: ACM200616406-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-N-Me-His(Trt)-OH | Building block for introduction of N-α-methyl-histidine amino-acid residues by Fmoc SPPS. Product has poor solubility but does dissolve upon activation in NMP with HBTU/DIPEA. Uses: Peptide synthesis. Additional or Alternative Names: Fmoc-N-Me-His(Trt)-OH, N-α-Fmoc-N-α-methyl-im-trityl-L-histidine. Product Category: Amino Acids. CAS No. 1217840-61-3. Mole weight: 633.73. Product ID: ACM1217840613-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-N-Me-His(Trt)-OH | Fmoc-N-Me-His(Trt)-OH (Fmoc-MeHis(Trt)-OH) is a is an amino acid derivative containing amino and carboxyl groups. Fmoc-N-Me-His(Trt)-OH for the synthesis of Fmoc-MeHis (Trt) -Leu-OH [1]. Uses: Scientific research. Group: Peptides. Alternative Names: Fmoc-MeHis(Trt)-OH. CAS No. 1217840-61-3. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-W142161. | |
| Fmoc-N-Me-Homocys(Trt)-OH | Fmoc-N-Me-Homocys(Trt)-OH has been incorporated in cyclic somatostatin analogs. Synonyms: (S)-2-(N-Fmoc-N-methyl-amino)-4-tritylsulfanyl-butyric acid; (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-4-(tritylthio)butanoic acid; N-{[(9H-Fluoren-9-yl)methoxy]carbonyl}-N-methyl(triphenyl)-L-methionine; N-alpha-(9-Fluorenylmethyloxycarbonyl)-N-alpha-methyl-S-trityl-L-homocysteine; MeHcy. Grades: 95%. CAS No. 526210-71-9. Molecular formula: C39H35NO4S. Mole weight: 613.76. | |
| Fmoc-N-Me-Ile-OH | Building block for introduction of N-α-methyl-isoleucine amino-acid residues by Fmoc SPPS. Uses: Peptide synthesis. Additional or Alternative Names: Fmoc-N-Me-Ile-OH, N-α-Fmoc-N-α-methyl-L-isoleucine. Product Category: Amino Acids. CAS No. 138775-22-1. Mole weight: 367.44. Product ID: ACM138775221. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-N-Me-L-Cys(Trt)-OH | Fmoc-N-Me-L-Cys(Trt)-OH. Group: Biochemicals. Alternative Names: Fmoc-N-Me-Cys(Trt)-OH. Grades: Highly Purified. CAS No. 944797-51-7. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C38H33NO4S. US Biological Life Sciences. | Worldwide |
| Fmoc-N-Me-Leu-OH | Fmoc-N-Me-Leu-OH can be used for peptide coupling reactions. Synonyms: N-(fluorenylmethoxycarbonyl)-N-methyl-L-leucine; Fmoc-N-methyl-L-leucine; N-Fmoc-N-methyl-L-leucine; FMOC-MeLeu-OH; L-Leucine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methyl-; Fmoc-N-alpha-methyl-L-leucine; N-Methyl-N-Fmoc-L-Leu-OH. Grades: ≥99.5% by Chiral HPLC. CAS No. 103478-62-2. Molecular formula: C22H25NO4. Mole weight: 367.44. | |
| Fmoc-N-Me-Leu-OH | Fmoc-N-Me-Leu-OH, an N-Fmoc-N-methyl amino acid, is available for the peptide-coupling reaction. Uses: Scientific research. Group: Signaling pathways. CAS No. 103478-62-2. Pack Sizes: 10 mM * 1 mL; 1 g. Product ID: HY-W008558. | |
| Fmoc-N-Me-Leu-OH | Building block for introduction of N-α-methyl-leucine amino-acid residues by Fmoc SPPS. Uses: Peptide synthesis. Additional or Alternative Names: Fmoc-N-Me-Leu-OH, N-α-Fmoc-N-α-methyl-L-leucine. Product Category: Amino Acids. CAS No. 103478-62-2. Molecular formula: C22H25NO4. Mole weight: 367.44. Product ID: ACM103478622. Alfa Chemistry ISO 9001:2015 Certified. Categories: (2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}(methyl)amino)-4-methylpentanoic acid. | |
| Fmoc-N-MeLeu-Wang Resin | Fmoc-N-MeLeu-Wang Resin. Group: Fmoc-amino acid-wang resins. Pack Sizes: 1g, 5g. | |
| Fmoc-N-Me-L-Lys(Boc)-OH | Fmoc-N-Me-L-Lys(Boc)-OH. Group: Biochemicals. Grades: Highly Purified. CAS No. 197632-76-1. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C27H34N2O6. US Biological Life Sciences. | Worldwide |
| Fmoc-N-Me-L-Met-OH | Fmoc-N-Me-L-Met-OH. Group: Biochemicals. Alternative Names: Fmoc-N-methyl-L-methionine. Grades: Highly Purified. CAS No. 84000-12-4. Pack Sizes: 250mg, 500mg, 1g. US Biological Life Sciences. | Worldwide |
| Fmoc-N-Me-L-Met-OH 99+% (HPLC) | Fmoc-N-Me-L-Met-OH 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100mg, 250mg, 1g. US Biological Life Sciences. | Worldwide |
| Fmoc-N-Me-L-norvaline | Fmoc-N-Me-L-norvaline. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
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