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| Product | Description | |
|---|---|---|
| Boc-Gly-Gly-Gly-OH ≥97.5% (HPLC) | Boc-Gly-Gly-Gly-OH ≥97.5% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. |  Worldwide |
| Boc-Gly-Gly-OH | Boc-Gly-Gly-OH. Group: Biochemicals. Alternative Names: N-(2-N-Boc-aminoacetyl)glycine; Boc-L-glycyl glycine. Grades: Highly Purified. CAS No. 31972-52-8. Pack Sizes: 5g, 10g, 25g, 50g, 100g. US Biological Life Sciences. | Worldwide |
| Boc-Gly-Gly-OH | Boc-Gly-Gly-OH. Synonyms: N-(2-N-Boc-aminoacetyl)glycine. Grade: ≥ 98% (HPLC). CAS No. 31972-52-8. Molecular formula: C9H16N2O5. Mole weight: 232.24. |  |
| Boc-Gly-Gly-OH 98+% (HPLC) | Boc-Gly-Gly-OH 98+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 5g, 25g, 100g. US Biological Life Sciences. | Worldwide |
| Boc-Gly-Gly-OSu | Boc-Gly-Gly-OSu. Synonyms: Boc-Gly-Gly-NHS ester; Glycine, N-[(1,1-dimethylethoxy)carbonyl]glycyl-, 2,5-dioxo-1-pyrrolidinyl ester. CAS No. 29248-48-4. Molecular formula: C13H19N3O7. Mole weight: 329.31. | |
| Boc-Gly-Gly-Phe-Gly-OH | Boc-Gly-Gly-Phe-Gly-OH is a self-assembly of N- and C-protected tetrapeptide. It is also a protease-cleavable linker for antibody-drug conjugates (ADCs). Synonyms: N-tert-butoxycarbonyl-glycyl-glycyl-L-phenylalanyl-glycine; N-(tert-butoxycarbonyl)-glycylglycyl-L-phenylalanylglycine; (S)-12-Benzyl-2,2-dimethyl-4,7,10,13-tetraoxo-3-oxa-5,8,11,14-tetraazahexadecan-16-oic acid. Grade: >95%. CAS No. 187794-49-6. Molecular formula: C20H28N4O7. Mole weight: 436.46. | |
| Boc-Gly-Gly-Phe-Gly-OH | Boc-Gly-Gly-Phe-Gly-OH, a self-assembly of N- and C-protected tetrapeptide, is a protease cleavable linker used for the antibody-drug conjugate (ADC). Uses: Scientific research. Group: Peptides. CAS No. 187794-49-6. Pack Sizes: 100 mg; 250 mg; 1 g; 5 g; 10 g. Product ID: HY-P1449. |  |
| Boc-Gly-Gly-Phe-Gly-OH TFA | Boc-Gly-Gly-Phe-Gly-OH TFA, a self-assembly of N- and C-protected tetrapeptide, is a protease cleavable linker used for the antibody-drug conjugate (ADC). Synonyms: Boc-Gly-Gly-Phe-Gly-OH trifluoroacetic acid; N-tert-butoxycarbonyl-glycyl-glycyl-L-phenylalanyl-glycine trifluoroacetic acid. Grade: >98%. Molecular formula: C22H29F3N4O9. Mole weight: 550.48. | |
| Boc-Gly-Gly-Tyr-OH | Boc-Gly-Gly-Tyr-OH. Molecular formula: C18H25N3O7. Mole weight: 395.4. | |
| Boc-Gly-Leu-OH | Boc-Gly-Leu-OH. Synonyms: (2S)-4-methyl-2-[[2-[(2-methylpropan-2-yl)oxycarbonylamino]acetyl]amino]pentanoic acid. Grade: ≥ 95%. CAS No. 51871-42-2. Molecular formula: C13H24N2O5. Mole weight: 288.30. | |
| Boc-Gly-OH | Standard building block for introduction of glycine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Additional or Alternative Names: Boc-Gly-OH, N-α-t.-Boc-glycine. Product Category: Amino Acids. CAS No. 4530-20-5. Molecular formula: C7H13NO4. Mole weight: 175.18. Product ID: ACM4530205. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Boc-Gly-OH-[1-13C] | Boc-Gly-OH-[1-13C] is a labelled Glycine-N-T-BOC. Glycine is one of the non-essential amino acids for humans. Glycine is an inhibitory neurotransmitter in the central nervous system. Synonyms: Glycine-N-T-Boc 1-13C; Glycine-1-13C-N-T-BOC. Grade: 98% by CP; 99% atom 13C. CAS No. 97352-64-2. Molecular formula: C6[13C]H13NO4. Mole weight: 176.18. | |
| Boc-Gly-OH-1-13C | 99 atom % 13C. Group: Fluorescence/luminescence spectroscopy. |  |
| Boc-Gly-OH-1-13C | Boc-Gly-OH-1-13C. Uses: Peptide synthesis. Additional or Alternative Names: N-(tert-Butoxycarbonyl)glycine-1-13C, Glycine-1-13C, N-t-Boc derivative. Product Category: Amino Acids. CAS No. 97352-64-2. Molecular formula: Boc-NHCH213CO2H. Mole weight: 176.18. Canonical SMILES: CC(C)(C)OC(=O)NC[13C](O)=O. Product ID: ACM97352642-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Boc-Gly-OH-1-13C,15N | Boc-Gly-OH-1-13C,15N. Uses: Peptide synthesis. Additional or Alternative Names: N-(tert-Butoxycarbonyl)glycine-1-13C,15N, Glycine-1-13C,15N, N-t-Boc derivative. Product Category: Amino Acids. CAS No. 145143-00-6. Molecular formula: Boc-15NHCH213CO2H. Mole weight: 177.17. Canonical SMILES: CC(C)(C)OC(=O)[15NH]C[13C](O)=O. Product ID: ACM145143006. Alfa Chemistry ISO 9001:2015 Certified. | |
| Boc-Gly-OH-13C2,15N | Boc-Gly-OH-13C2,15N. Uses: Peptide synthesis. Additional or Alternative Names: N-(tert-Butoxycarbonyl)glycine-13C2,15N, Glycine-13C2,15N, N-t-Boc derivative. Product Category: Amino Acids. CAS No. 145142-99-0. Molecular formula: Boc-15NH13CH213CO2H. Mole weight: 178.16. Canonical SMILES: CC(C)(C)OC(=O)[15NH][13CH2][13C](O)=O. Product ID: ACM145142990-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Boc-Gly-OH-15N | 98 atom % 15N, 99% (CP). Group: Fluorescence/luminescence spectroscopy. | |
| Boc-Gly-OH-15N | Boc-Gly-OH-15N. Uses: Peptide synthesis. Additional or Alternative Names: N-(tert-Butoxycarbonyl)glycine-15N, 15N Labeled Boc-Gly-OH, 15N Labeled N-(tert-butoxycarbonyl)glycine, Glycine-15N, N-t-Boc derivative. Product Category: Amino Acids. CAS No. 106665-75-2. Molecular formula: Boc-15NHCH2CO2H. Mole weight: 176.18. Canonical SMILES: CC(C)(C)OC(=O)[15NH]CC(O)=O. Product ID: ACM106665752-2. Alfa Chemistry ISO 9001:2015 Certified. | |
| Boc-Gly-OH-[2-13C] | Boc-Gly-OH-[2-13C] is a labelled Glycine-N-T-BOC. Glycine is one of the non-essential amino acids for humans. Glycine is an inhibitory neurotransmitter in the central nervous system. Synonyms: Glycine-N-T-Boc 2-13C. Grade: 98% by CP; 99% atom 13C. CAS No. 145143-02-8. Molecular formula: C6[13C]H13NO4. Mole weight: 176.18. | |
| Boc-Gly-OH-[2-13C,15N] | Boc-Gly-OH-[2-13C,15N] is a labelled Glycine-N-T-BOC. Glycine is one of the non-essential amino acids for humans. Glycine is an inhibitory neurotransmitter in the central nervous system. Synonyms: Glycine-N-T-Boc 2-13C,15N; N-(Tert-butoxycarbonyl)glycine-2-13C-15N. Grade: 98% by CP; 99% atom 13C; 98% atom 15N. CAS No. 145143-01-7. Molecular formula: C6[13C]H13[15N]O4. Mole weight: 177.17. | |
| Boc-Gly-OH-2-13C,15N | Boc-Gly-OH-2-13C,15N. Uses: Peptide synthesis. Additional or Alternative Names: N-(tert-Butoxycarbonyl)glycine-2-13C,15N, Glycine-2-13C,15N, N-t-Boc derivative. Product Category: Amino Acids. CAS No. 145143-01-7. Molecular formula: Boc-15NH13CH2CO2H. Mole weight: 177.17. Canonical SMILES: CC(C)(C)OC(=O)[15NH][13CH2]C(O)=O. Product ID: ACM145143017-2. Alfa Chemistry ISO 9001:2015 Certified. | |
| Boc-Gly-OH-2-13C,15N | 99 atom % 13C, 98 atom % 15N. Group: Fluorescence/luminescence spectroscopy. | |
| Boc-Gly-OH-2,2-d2 | Boc-Gly-OH-2,2-d2. Uses: Peptide synthesis. Additional or Alternative Names: N-(tert-Butoxycarbonyl)glycine-2,2-d2, Glycine-2,2-d2, N-t-Boc derivative. Product Category: Amino Acids. CAS No. 42492-65-9. Molecular formula: Boc-NHCD2CO2H. Mole weight: 177.19. Canonical SMILES: [2H]C([2H])(NC(=O)OC(C)(C)C)C(O)=O. Product ID: ACM42492659-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Boc-Gly-OH-2,2-d2 | 98 atom % D. Group: Fluorescence/luminescence spectroscopy. | |
| Boc-Gly-Oipr | Boc-Gly-Oipr. Synonyms: N-Boc-glycine isopropylester; Isopropyl (tert-butoxycarbonyl)glycinate; N-[(1,1-Dimethylethoxy)carbonyl]glycine 1-methylethyl ester; Glycine, N-[(1,1-dimethylethoxy)carbonyl]-, 1-methylethyl ester. CAS No. 197579-95-6. Molecular formula: C10H19NO4. Mole weight: 217.26. | |
| Boc-Gly-Pro-OH | Boc-Gly-Pro-OH. Synonyms: Boc-L-glycyl proline. Grade: ≥ 99% (HPLC). CAS No. 14296-92-5. Molecular formula: C12H20N2O5. Mole weight: 272.3. | |
| Boc-Gly-Pro-OH | Boc-Gly-Pro-OH. Group: Biochemicals. Alternative Names: Boc-L-glycyl proline. Grades: Highly Purified. CAS No. 14296-92-5. Pack Sizes: 2g, 5g, 10g, 25g. US Biological Life Sciences. | Worldwide |
| Boc-Gly-Pro-OH | Boc-Gly-Pro-OH is a Glycine (HY-Y0966) derivative [1]. Uses: Scientific research. Group: Peptides. CAS No. 14296-92-5. Pack Sizes: 5 g; 10 g; 25 g; 100 g. Product ID: HY-W018717. | |
| Boc-Gly-Pro-OH 99+% (HPLC) | Boc-Gly-Pro-OH 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| Boc-Gly-Tyr-Ome | Boc-Gly-Tyr-Ome. CAS No. 65160-62-5. Molecular formula: C17H24N2O6. Mole weight: 352.38. | |
| Boc-Gly-Val-OH | Boc-Gly-Val-OH. Uses: Peptide synthesis. Product Category: Amino Acids. CAS No. 28334-73-8. Mole weight: 274.31. Canonical SMILES: OC([C@H](C(C)C)NC(CNC(OC(C)(C)C)=O)=O)=O. Product ID: ACM28334738. Alfa Chemistry ISO 9001:2015 Certified. | |
| BOC-GRR-AMC | BOC-GRR-AMC is cleaved by type II Metacaspases Atmc4 and Atmc9 of Arabidopsis thaliana. It is a substrate for flavivirus proteases such as West Nile virus protease, yellow fever virus NS3 protease, and dengue virus NS2B-NS3 protease. Synonyms: tert-butyl 2-((S)-5-guanidino-1-((S)-5-guanidino-1-(4-methyl-2-oxo-2H-chromen-7-ylamino)-1-oxopentan-2-ylamino)-1-oxopentan-2-ylamino)-2-oxoethylcarbamate. Grade: 95%. CAS No. 113866-14-1. Molecular formula: C29H44N10O7. Mole weight: 644.72. | |
| Boc-GRR-AMC TFA | Boc-GRR-AMC (TFA) is a tri-peptide Substrate. BOC-GRR-AMC is cleaved by type II Metacaspases Atmc4 and Atmc9 of Arabidopsis thaliana. It is a substrate for flavivirus proteases such as West Nile virus protease, yellow fever virus NS3 protease, and dengue virus NS2B-NS3 protease. Grade: 98%. Molecular formula: C29H44N10O7.xC2HF3O2. Mole weight: 644.72 (free base). | |
| Boc-guanidine | Boc-guanidine. Group: Biochemicals. Grades: Highly Purified. CAS No. 219511-71-4. Pack Sizes: 2g, 5g, 10g, 25g. US Biological Life Sciences. | Worldwide |
| Boc-His(1-Me)-OH | Boc-His(1-Me)-OH. Synonyms: Boc-L-His(Nim-Me)-OH; Boc-His(τ-Me)-OH. Grade: ≥ 99% (HPLC). CAS No. 61070-20-0. Molecular formula: C12H19N3O4. Mole weight: 269.30. | |
| Boc-His(1-Me)-OH | Boc-His(1-Me)-OH. Group: Biochemicals. Alternative Names: Boc-L-His(Nim-Me)-OH; Boc-His(?-Me)-OH. Grades: Highly Purified. CAS No. 61070-20-0. Pack Sizes: 25mg, 50mg, 100mg, 250mg, 500mg. Molecular Formula: C12H19N3O4. US Biological Life Sciences. | Worldwide |
| Boc-His(1-Me)-OH 99+% (HPLC) | Boc-His(1-Me)-OH 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100mg, 250mg, 1g. US Biological Life Sciences. | Worldwide |
| Boc-His(3-Bom)-OH | Boc-His(3-Bom)-OH. Synonyms: Boc-L-His(p-Bom)-OH; Boc-N-p-benzyloxymethyl-L-histidine; Nalpha-Boc-3-[(benzyloxy)methyl]-L-histidine. Grade: ≥ 98.5% (HPLC). CAS No. 79950-65-5. Molecular formula: C19H25N3O5. Mole weight: 375.43. | |
| Boc-His(3-Bom)-OH 98+% (HPLC) | Boc-His(3-Bom)-OH 98+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| Boc-His(3-Me)-OH | Boc-His(3-Me)-OH. Synonyms: Boc-L-His(p-Me)-OH; Boc-N-p-methyl-L-histidine; (S)-2-(Boc-amino)-3-(1-methyl-5-imidazolyl)propanoic Acid. Grade: ≥ 99% (HPLC). CAS No. 61070-22-2. Molecular formula: C12H19N3O4. Mole weight: 269.30. | |
| Boc-His(3-Me)-OH | Boc-His(3-Me)-OH. Group: Biochemicals. Alternative Names: Boc-L-His(p-Me)-OH; Boc-N-p-methyl-L-histidine. Grades: Highly Purified. CAS No. 61070-22-2. Pack Sizes: 100mg, 250mg, 500mg, 1g. US Biological Life Sciences. | Worldwide |
| Boc-His(3-Me)-OH 99+% (HPLC) | Boc-His(3-Me)-OH 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100mg, 250mg, 1g. US Biological Life Sciences. | Worldwide |
| Boc-His(Boc)-Aib-OH | Boc-His(Boc)-Aib-OH. CAS No. 1169630-98-1. Molecular formula: C20H32N4O7. Mole weight: 440.50. | |
| Boc-His(Boc)-OH Benzene | Boc-His(Boc)-OH Benzene. Synonyms: N-α,N-τ-Di(t-butoxycarbonyl)-L-histidine benzene solvate; (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-[1-[(2-methylpropan-2-yl)oxycarbonyl]imidazol-4-yl]propanoic acid benzene solvate. Molecular formula: C22H31N3O6. Mole weight: 433.51. | |
| Boc-His(Boc)-OH. DCHA | A protected histidine derivative for only the critical coupling step in Boc SPPS. After coupling the two Boc-groups are cleaved simultaneously by TFA. Associated Protocols and Technical Articles Cleavage and Deprotection Protocols for Boc SPPS. Uses: Peptide synthesis. Additional or Alternative Names: Boc-His(Boc)-OH. DCHA, N-α-N-im-di-t.-Boc-L-histidine dicyclohexylammonium salt. Product Category: Amino Acids. CAS No. 31687-58-8. Mole weight: 355.39. Product ID: ACM31687588. Alfa Chemistry ISO 9001:2015 Certified. | |
| Boc-His(Boc)-OMe | Boc-His(Boc)-OMe. Synonyms: Tert-butyl 4-(2-((tert-butoxycarbonyl)amino)-3-methoxy-3-oxopropyl)-1H-imidazole-1-carboxylate. CAS No. 20898-43-5. Molecular formula: C17H27N3O6. Mole weight: 369.4. | |
| Boc-His(Bom)-OH | Boc-His(Bom)-OH. Uses: Peptide synthesis. Product Category: Amino Acids. CAS No. 79950-65-5. Molecular formula: C19H25N3O5. Mole weight: 375.4. Purity: 0.97. IUPACName: (2S)-3-{1-[(benzyloxy)methyl]-1H-imidazol-5-yl}-2-[(tert-butoxycarbonyl)amino]propanoic acid. Density: 1.2±0.1 g/cm3. Product ID: ACM79950655. Alfa Chemistry ISO 9001:2015 Certified. | |
| Boc-His(Dnp)-OH IPA | Boc-His(Dnp)-OH IPA. Synonyms: N-α-(t-Butoxycarbonyl)-N-τ-(2,4-dinitrophenyl)-L-histidine isopropanol solvate. CAS No. 1260247-63-9. Molecular formula: C20H27N5O9. Mole weight: 481.47. | |
| Boc-His(Fmoc)-OH | Boc-His(Fmoc)-OH. Molecular formula: C26H27N3O6. Mole weight: 477.5. | |
| Boc-His-Gly-OH | Boc-His-Gly-OH. Synonyms: 2-[[(2S)-3-(1H-imidazol-5-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoyl]amino]acetic acid. CAS No. 1998701-32-8. Molecular formula: C13H20N4O5. Mole weight: 312.32. | |
| Boc-His-Met-OH | Boc-His-Met-OH. Grade: ≥ 98%. CAS No. 248921-84-8. Molecular formula: C16H26N4O5S. Mole weight: 386.47. | |
| Boc-His-Met-OH | Boc-His-Met-OH. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 250mg. US Biological Life Sciences. | Worldwide |
| Boc-His-Met-OH 99+% (TLC) | Boc-His-Met-OH 99+% (TLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100mg, 250mg. US Biological Life Sciences. | Worldwide |
| Boc-His(Mts)-aldehyde | Boc-His(Mts)-aldehyde. Synonyms: tert-butyl [(2R)-1-oxo-3-{1-[(2,4,6-trimethylphenyl)sulfonyl]-1H-imidazol-4-yl}propan-2-yl]carbamate; N-Boc-2(S)-2-amino-3-{1-[(2,4,6-trimethylphenyl)sulfonyl]-1H-imidazol-4-yl}propanal. CAS No. 1379797-43-9. Molecular formula: C20H27N3O5S. Mole weight: 421.51. | |
| Boc-His-OH | Building block for introduction of histidine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Additional or Alternative Names: Boc-His-OH, N-α-t.-Boc-L-histidine. Product Category: Amino Acids. CAS No. 17791-52-5. Mole weight: 255.27. Product ID: ACM17791525. Alfa Chemistry ISO 9001:2015 Certified. | |
| Boc-Histidinol(Tos) | Boc-Histidinol(Tos). Synonyms: Boc-His(1-Tos)-ol. CAS No. 1169760-85-3. Molecular formula: C18H25N3O5S. Mole weight: 395.5. | |
| Boc-His(Tos)-OH | Standard building block for introduction of histidine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Additional or Alternative Names: Boc-His(Tos)-OH, N-α-t.-Boc-N-im-tosyl-L-histidine. Product Category: Amino Acids. CAS No. 35899-43-5. Mole weight: 409.46. Product ID: ACM35899435-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Boc-His(Trt)-Aib-Gln(Trt)-Gly-Gly-OH | Boc-His(Trt)-Aib-Gln(Trt)-Gly-Gly-OH is a protected pentapeptide used in peptide synthesis. It includes histidine (His), α-aminoisobutyric acid (Aib), glutamine (Gln), and two glycine (Gly) residues. The Boc (tert-Butyloxycarbonyl) group protects the N-terminus of the histidine residue, while the Trt (Trityl) groups shield the side chains of histidine and glutamine, preventing premature reactions. The Aib residue adds conformational rigidity, and the two glycine residues at the C-terminus are free, indicated by -OH, allowing for further coupling or modifications. This peptide is designed to ensure controlled reactivity and stability throughout the synthesis process. Synonyms: HXQGG; N2-(2-((S)-2-((tert-Butoxycarbonyl)amino)-3-(1-trityl-1H-imidazol-4-yl)propanamido)-2-methylpropanoyl)-N5-trityl-L-glutaminylglycylglycine. Grade: ≥96%. Molecular formula: C62H66N8O9. Mole weight: 1067.26. | |
| Boc-His(Trt)-Aib-Gln(Trt)-Gly-OH | It is the PDC linker targeting moietie of peptide drug conjugates (PDCs). Synonyms: N2-(2-((S)-2-((tert-Butoxycarbonyl)amino)-3-(1-trityl-1H-imidazol-4-yl)propanamido)-2-methylpropanoyl)-N5-trityl-L-glutaminylglycine. Grade: 95%. CAS No. 3034670-38-4. Molecular formula: C60H63N7O8. Mole weight: 1010.19. | |
| Boc-His(Trt)-Aib-Gln(Trt)-OH | Boc-His(Trt)-Aib-Gln(Trt)-OH is a protected tripeptide used in peptide synthesis. The Boc (tert-Butoxycarbonyl) group protects the N-terminus of the histidine (His) residue, preventing it from reacting during synthesis. The side chain imidazole group of histidine and the amide group of glutamine (Gln) are protected by Trt (Trityl) groups, shielding these functional groups from unwanted reactions until selective deprotection is performed. Aib (α-aminoisobutyric acid), known for inducing helical structures, is the middle residue. The -OH at the C-terminus of glutamine indicates a free carboxyl group, allowing for further coupling or modifications. This peptide is used to incorporate histidine, Aib, and glutamine into peptides, with specific protections to ensure controlled and efficient peptide synthesis. Synonyms: HXQ; N2-(2-((S)-2-((tert-Butoxycarbonyl)amino)-3-(1-trityl-1H-imidazol-4-yl)propanamido)-2-methylpropanoyl)-N5-trityl-L-glutamine. Grade: ≥95%. Molecular formula: C58H60N6O7. Mole weight: 953.15. | |
| Boc-His(Trt)-Aib-Glu(OBtu)-Gly-OH | Boc-His(Trt)-Aib-Glu(OBtu)-Gly-OH. Synonyms: ((S)-5-(tert-Butoxy)-2-(2-((S)-2-((tert-butoxycarbonyl)amino)-3-(1-trityl-1H-imidazol-4-yl)propanamido)-2-methylpropanamido)-5-oxopentanoyl)glycine. CAS No. 1890228-73-5. Molecular formula: C45H56N6O9. Mole weight: 824.98. | |
| Boc-His(Trt)-Aib-Gly-OH | Boc-His(Trt)-Aib-Gly-OH is a protected tripeptide used in peptide synthesis. The Boc (tert-Butoxycarbonyl) group protects the N-terminus of the histidine (His) residue, preventing it from reacting during synthesis. The imidazole side chain of histidine is protected by a Trt (Trityl) group, which shields it from unwanted reactions until deprotection is performed. Aib (α-aminoisobutyric acid), known for its helical structure-inducing properties, is the middle residue. Gly (Glycine), the final amino acid, has a free carboxyl group at the C-terminus, indicated by -OH, allowing for further peptide coupling or modifications. This peptide is used to introduce histidine, Aib, and glycine into peptide sequences, with specific protections to ensure controlled and efficient peptide synthesis. Synonyms: HXG; (S)-(2-(2-((tert-Butoxycarbonyl)amino)-3-(1-trityl-1H-imidazol-4-yl)propanamido)-2-methylpropanoyl)glycine. Grade: ≥97%. Molecular formula: C36H41N5O6. Mole weight: 639.75. | |
| Boc-His(Trt)-Aib-OH | Boc-His(Trt)-Aib-OH, a highly specialized peptide synthesis reagent employed within the biomedical industry, presents a powerful capability for the creation of peptide sequences inclusive of unconventional amino acids. Its steadfast utilization helps to promote the generation of distinct and optimal peptide architectures, critical for the progression of targeted drug development, including the likes of Alzheimer's disease, cancer and many other diseases. Synonyms: (S)-2-(2-((tert-Butoxycarbonyl)amino)-3-(1-trityl-1H-imidazol-4-yl)propanamido)-2-methylpropanoic acid. CAS No. 2061897-68-3. Molecular formula: C34H38N4O5. Mole weight: 582.7. | |
| Boc-His(Trt)-Aib-OH | Boc-His(Trt)-Aib-OH. Alternative Names: (Tert-Butoxy)CarbonylL-His(Trt)-Aib-OH;BOC-L-HIS(TRT)-AIB-OH;2-[(2S)-2-{[(tert-butoxy)carbonyl]amino}-3-[1-(triphenylmethyl)-1H-imidazol-4-Chemicalbookyl]propanamido]-2-methylpropanoicacid;(S)-2-(2-((tert-Butoxycarbonyl)amino)-3-(1-trityl-1H-imidazol-4-yl)propanamido)-2-methylpropanoicacid. CAS No. 2061897-68-3. Product ID: INT2061897683. Mole weight: 582.7. InChIKey: POZCMPSLNOUKQN-NPFCIKOQNA-N. SMILES: C(C1C=CC=CC=1)(C1C=CC=CC=1)(C1C=CC=CC=1)N1C=NC(C[C@H](NC(=O)OC(C)(C)C)C(=O)NC(C)(C)C(=O)O)=C1 |&1:24,r|. Category: Intermediates. |  |
| Boc-His(Trt)-Gln(Trt)-Gly-OH | Boc-His(Trt)-Gln(Trt)-Gly-OH is a protected tripeptide used in peptide synthesis. The Boc (tert-Butoxycarbonyl) group protects the N-terminus of the histidine (His) residue, preventing premature reactions during synthesis. The side chain imidazole group of histidine and the amide group of glutamine (Gln) are protected by Trt (Trityl) groups, shielding these functional groups until selective deprotection is required. Gly (Glycine), the final amino acid in the sequence, has a free carboxyl group at the C-terminus, indicated by -OH, which allows for further peptide coupling or modifications. This compound is used to introduce histidine, glutamine, and glycine into peptides, with controlled protection of functional groups to ensure efficient and precise peptide synthesis. Synonyms: HQG; N2-(Na-(tert-Butoxycarbonyl)-Nt-trityl-L-histidyl)-N5-trityl-L-glutaminylglycine. Grade: ≥96%. Molecular formula: C56H56N6O7. Mole weight: 925.10. | |
| Boc-His(Trt)-Gly-OH | Boc-His(Trt)-Gly-OH. Synonyms: 2-[[(2S)-2-[(2-Methylpropan-2-yl)oxycarbonylamino]-3-(1-tritylimidazol-4-yl)propanoyl]amino]acetic acid. CAS No. 1428125-85-2. Molecular formula: C32H34N4O5. Mole weight: 554.6. | |
| Boc-His(Trt)-OH | A protected histidine derivative for only the critical coupling step in Boc SPPS. After coupling the Boc- and Trt-groups are cleaved simultaneously by TFA. Uses: Peptide synthesis. Additional or Alternative Names: Boc-His(Trt)-OH, N-α-t.-Boc-N-im-trityl-L-histidine. Product Category: Amino Acids. CAS No. 32926-43-5. Mole weight: 497.58. Product ID: ACM32926435. Alfa Chemistry ISO 9001:2015 Certified. | |
| Boc-His(Trt)-OH | Boc-His(Trt)-OH is a histidine derivative [1]. Uses: Scientific research. Group: Peptides. CAS No. 32926-43-5. Pack Sizes: 25 g; 100 g; 500 g. Product ID: HY-W010788. | |
| Boc-His(Z)-OH | Boc-His(Z)-OH. Group: Biochemicals. Alternative Names: Boc-Nim-Z-L-histidine. Grades: Highly Purified. CAS No. 50305-43-6. Pack Sizes: 1g, 2g, 5g, 10g, 25g. US Biological Life Sciences. | Worldwide |
| Boc-His(Z)-OH | Boc-His(Z)-OH. Synonyms: Boc-Nim-Z-L-Histidine; (S)-3-(1-((Benzyloxy)carbonyl)-1H-imidazol-4-yl)-2-((tert-butoxycarbonyl)amino)propanoic acid; Nt-((benzyloxy)carbonyl)-Na-(tert-butoxycarbonyl)-L-histidine. Grade: ≥ 99% (HPLC). CAS No. 50305-43-6. Molecular formula: C19H23N3O6. Mole weight: 389.41. | |
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