BOC Sciences 8 - Products

BOC Sciences provides a wide range of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecule and chiral compounds.

Product
Boc-D-Trp-OMe Boc-D-Trp-OMe. Alternative Names: Methyl (2R)-3-(1H-indol-3-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate. CAS No. 151872-21-8. Molecular formula: C17H22N2O4. Mole weight: 318.4. BOC Sciences 8
Boc-D-Tryptophanol Boc-D-Tryptophanol. Alternative Names: (R)-tert-Butyl(1-hydroxy-3-(1H-indol-3-yl)propan-2-yl)carbamate; N-Boc-D-tryptophanol; tert-butyl N-[(2R)-1-hydroxy-3-(1H-indol-3-yl)propan-2-yl]carbamate. Grades: ≥ 95%. CAS No. 158932-00-4. Molecular formula: C16H22N2O3. Mole weight: 290.30. BOC Sciences 8
Boc-D-Tyr(3-I)-OH Boc-D-Tyr(3-I)-OH. Alternative Names: Boc-3-iodo-D-tyr-OH. CAS No. 478183-68-5. Molecular formula: C14H18NO5I. Mole weight: 407.2. BOC Sciences 8
Boc-D-Tyr(All)-OH DCHA Boc-D-Tyr(All)-OH DCHA. Molecular formula: C17H23NO5·C12H23N. Mole weight: 502.7. BOC Sciences 8
Boc-D-Tyr-Oet Boc-D-Tyr-Oet. Alternative Names: Boc-D-Tyr-Oet-OH; Ethyl (tert-butoxycarbonyl)-D-tyrosinate. CAS No. 1241680-28-3. Molecular formula: C16H23NO5. Mole weight: 309.36. BOC Sciences 8
Boc-D-tyrosine Boc-D-tyrosine. Alternative Names: Boc-D-Tyr-OH; N-(tert-Butoxycarbonyl)-D-tyrosine. Grades: ≥ 98% (HPLC). CAS No. 70642-86-3. Molecular formula: C14H19NO5. Mole weight: 281.30. BOC Sciences 8
Boc-D-tyrosine methyl ester Boc-D-tyrosine methyl ester. Alternative Names: Boc-D-Tyr-Ome; (R)-Methyl 2-((tert-butoxycarbonyl)amino)-3-(4-hydroxyphenyl)propanoate. Grades: ≥ 98% (HPLC). CAS No. 76757-90-9. Molecular formula: C15H21NO5. Mole weight: 295.34. BOC Sciences 8
Boc-D-Tyrosinol Boc-D-Tyrosinol. Alternative Names: Boc-D-Tyr-ol; (R)-tert-Butyl (1-hydroxy-3-(4-hydroxyphenyl)propan-2-yl)carbamate. Grades: ≥ 99% (HPLC). CAS No. 247018-46-8. Molecular formula: C14H21NO4. Mole weight: 267.33. BOC Sciences 8
Boc-D-Tyr(OtBu)-Aib-Gln(Trt)-Gly-OH Boc-D-Tyr(OtBu)-Aib-Gln(Trt)-Gly-OH is a protected tetrapeptide utilized in peptide synthesis. The Boc (tert-Butoxycarbonyl) group safeguards the N-terminus of the D-tyrosine (D-Tyr) residue, while the OtBu (tert-butyl) group protects the hydroxyl group on the D-tyrosine's side chain, preventing premature reactions during synthesis. The second residue, Aib (α-aminoisobutyric acid), is known for its ability to induce helical conformations in peptides. The Gln (Glutamine) residue has its side chain protected by a Trt (Trityl) group, allowing for selective deprotection later in the synthesis process. The final residue, Gly (Glycine), has a free carboxyl group at the C-terminus, denoted by -OH, which can be used for further coupling or modifications. This peptide is specifically designed to incorporate D-tyrosine, Aib, glutamine, and glycine into peptide structures, with carefully selected protective groups to ensure controlled and efficient synthesis. Alternative Names: yXQG; N2-(2-((R)-3-(4-(tert-Butoxy)phenyl)-2-((tert-butoxycarbonyl)amino)propanamido)-2-methylpropanoyl)-N5-trityl-L-glutaminylglycine; Boc-D-Tyr(tBu)-Aib-Gln(Trt)-Gly-OH. Grades: ≥95%. Molecular formula: C48H59N5O9. Mole weight: 850.03. BOC Sciences 8
Boc-D-Tyr(OtBu)-Aib-Glu(OtBu)-Gly-OH Boc-D-Tyr(OtBu)-Aib-Glu(OtBu)-Gly-OH is a protected tetrapeptide used in peptide synthesis. The Boc (tert-Butoxycarbonyl) group protects the N-terminus of the D-tyrosine (D-Tyr) residue, preventing it from reacting during synthesis. The side chain hydroxyl group of D-tyrosine and the carboxyl group of glutamic acid (Glu) are protected by OtBu (tert-butyl) groups, which shield these functional groups until selective deprotection is needed. Aib (α-aminoisobutyric acid), known for its ability to induce helical structures, is the third residue, and Gly (Glycine), the final amino acid, has a free carboxyl group at the C-terminus, indicated by -OH, allowing for further coupling or modifications. This peptide incorporates D-tyrosine, Aib, glutamic acid, and glycine into peptide sequences, with specific protections to ensure controlled and efficient synthesis. Alternative Names: yXEG; ((S)-5-(tert-Butoxy)-2-(2-((R)-3-(4-(tert-Butoxy)phenyl)-2-((tert-butoxycarbonyl)amino)propanamido)-2-methylpropanamido)-5-oxopentanoyl)glycine; Boc-D-Tyr(tBu)-Aib-Glu(tBu)-Gly-OH. Grades: ≥90%. Molecular formula: C33H52N4O10. Mole weight: 664.80. BOC Sciences 8
Boc-D-Tyr(OtBu)-Aib-OH Boc-D-Tyr(OtBu)-Aib-OH is a protected dipeptide used in peptide synthesis. The Boc (tert-Butoxycarbonyl) group protects the N-terminus of the D-tyrosine (D-Tyr) residue, preventing unwanted reactions during synthesis. The hydroxyl group on the D-tyrosine side chain is protected by an OtBu (tert-butyl) group, safeguarding it from reactivity until selective deprotection is desired. Aib (α-aminoisobutyric acid) is the second amino acid in the sequence, a non-natural amino acid known for inducing helical structures in peptides. The -OH at the C-terminus indicates a free carboxyl group, allowing for further peptide coupling. This compound is utilized to introduce D-tyrosine and Aib into peptides, with specific protections ensuring controlled and selective synthesis while incorporating structural constraints. Alternative Names: Boc-D-Tyr(tBu)-Aib-OH; N-tert-Butoxycarbonyl-O4-tert-butyl-D-tyrosyl-alpha-methyl-alanine; (R)-2-(3-(4-(tert-Butoxy)phenyl)-2-((tert-butoxycarbonyl)amino)propanamido)-2-methylpropanoic acid. Grades: ≥95%. Molecular formula: C22H34N2O6. Mole weight: 422.52. BOC Sciences 8
Boc-D-Val-aldehyde Boc-D-Val-aldehyde. Alternative Names: N-Boc-2(R)-2-amino-3-methyl-butanal; tert-butyl N-[(2R)-3-methyl-1-oxobutan-2-yl]carbamate; tert-butyl-1-formyl-2-methylpropylcarbamate. CAS No. 106391-88-2. Molecular formula: C10H19NO3. Mole weight: 201.26. BOC Sciences 8
Boc-D-valine Boc-D-valine. Alternative Names: Boc-D-Val-OH. Grades: ≥ 99% (HPLC). CAS No. 22838-58-0. Molecular formula: C10H19NO4. Mole weight: 217.30. BOC Sciences 8
Boc-D-valine 4-oxymethylphenylacetamidomethyl resin Boc-D-valine 4-oxymethylphenylacetamidomethyl resin. Alternative Names: Boc-D-Val-PAM resin. BOC Sciences 8
Boc-D-valine Merrifield resin Boc-D-valine Merrifield resin. Alternative Names: Boc-D-Val-Merrifield resin. BOC Sciences 8
Boc-D-Valinol Boc-D-Valinol (CAS# 106391-87-1) is a useful research chemical compound. Alternative Names: Boc-D-Val-ol; N-Boc-D-valinol; N-(tert-Butoxycarbonyl)-D-valinol; tert-butyl N-[(2R)-1-hydroxy-3-methylbutan-2-yl]carbamate. Grades: ≥ 97 % (NMR). CAS No. 106391-87-1. Molecular formula: C10H21NO3. Mole weight: 203.30. BOC Sciences 8
Boc-D-Val-Ome Boc-D-Val-Ome. Alternative Names: Boc-D-valine methyl ester; D-Boc valine methyl ester; (R)-methyl 2-(tert-butoxycarbonylamino)-3-methylbutanoate; Boc D Val Ome. Grades: 95%. CAS No. 106391-85-9. Molecular formula: C11H21NO4. Mole weight: 231.29. BOC Sciences 8
Boc-E-FMK Boc-E-FMK is a cell-permeable, irreversible pan-caspase inhibitor. Alternative Names: Boc-Glu-FMK; Boc-E-Fluoromethyl Ketone; Boc-E(OMe)-FMK. Grades: ≥95%. Molecular formula: C12H20FNO5. Mole weight: 277.29. BOC Sciences 8
Boc-ε-azido-Nle-OH Boc-ε-azido-Nle-OH is a click chemistry reagent containing an azide group. Alternative Names: Boc-Lys(N3)-OH; N-α-t-Butyloxycarbonyl-epsilon-azido-L-lysine; N-α-t-Butyloxycarbonyl-epsilon-azido-L-norleucine; (S)-2-t-Butyloxycarbonylamino-6-azidohexanoic acid; 6-Azido-N-Boc-L-Norleucine; (S)-6-azido-2-(Boc-amino)hexanoic acid; Boc-6-azido-L-norleucine; Nα-Boc-Nε-Azido-L-Lysine; N-tert-butoxycarbonyl-6-azido-L-norleucine. Grades: ≥95%. CAS No. 846549-33-5. Molecular formula: C11H20N4O4. Mole weight: 272.31. BOC Sciences 8
Boc,Et-Glycinol Boc,Et-Glycinol. Alternative Names: tert-butyl N-ethyl-N-(2-hydroxyethyl)carbamate. Grades: ≥ 95%. CAS No. 152192-95-5. Molecular formula: C9H19NO3. Mole weight: 189.25. BOC Sciences 8
Boc-GHK-OH Boc-GHK-OH. Alternative Names: Boc-Gly-His-Lys-OH; N-tert-butoxycarbonyl-glycyl-L-histidyl-L-lysine. Molecular formula: C19H32N6O6. Mole weight: 440.49. BOC Sciences 8
BOC-GLN-ALA-ARG-AMC HCL BOC-GLN-ALA-ARG-AMC is a highly reactive substrate for trypsin. Alternative Names: Boc-QAR-AMC. Grades: 95%. CAS No. 201849-55-0. Molecular formula: C29H43ClN8O8. Mole weight: 667.15. BOC Sciences 8
Boc-Gln-Ala-Arg-pNA Boc-Gln-Ala-Arg-pNA is a chromogenic substrate for trypsin and matriptase-2. Alternative Names: Boc-QAR-pNA; L-Argininamide, N2-[(1,1-dimethylethoxy)carbonyl]-L-glutaminyl-L-alanyl-N-(4-nitrophenyl)-; N2-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-glutaminyl-L-alanyl-N-(4-nitrophenyl)-L-argininamide; N-Boc-Gln-Ala-Arg-p-nitroanilide. Grades: ≥95% by HPLC. CAS No. 1926163-47-4. Molecular formula: C25H39N9O8. Mole weight: 593.63. BOC Sciences 8
Boc-Gln-Arg-Arg-AMC Boc-QRR-AMC is a substrate for the transmembrane serine protease hepsin, also is used for assaying kexin. Alternative Names: Boc-Gln-Arg-Arg-Mca; tert-butyl (S)-5-amino-1-((S)-5-guanidino-1-((S)-5-guanidino-1-(4-methyl-2-oxo-2H-chromen-7-ylamino)-1-oxopentan-2-ylamino)-1-oxopentan-2-ylamino)-1,5-dioxopentan-2-ylcarbamate; Boc-QRR-AMC. Grades: 95%. CAS No. 109376-05-8. Molecular formula: C32H49N11O8. Mole weight: 715.81. BOC Sciences 8
Boc-Gln-Gln-OH Boc-Gln-Gln-OH. Alternative Names: (2S)-5-amino-2-[[(2S)-5-amino-2-[(2-methylpropan-2-yl)oxycarbonylamino]-5-oxopentanoyl]amino]-5-oxopentanoic acid. Grades: ≥ 99.9% (GC, Chiral purity). CAS No. 250290-76-7. Molecular formula: C15H26N4O7. Mole weight: 374.39. BOC Sciences 8
Boc-Gln-Gly-Arg-AMC Boc-Gln-Gly-Arg-AMC is a peptide substrate for coagulation factor XIIa and trypsin. Alternative Names: Boc-Gln-Gly-Arg-MCA. CAS No. 113865-85-3. Molecular formula: C28H40N8O8. Mole weight: 616.67. BOC Sciences 8
BOC-GLN-GLY-ARG-AMC HCL A fluorogenic substrate for coagulation factor XIIa and trypsin. Alternative Names: N-tert-BOC-Gln-Gly-Arg 7-amido-4-methylcoumarin HCl. Grades: 95%. CAS No. 133448-21-2. Molecular formula: C28H41ClN8O8. Mole weight: 653.13. BOC Sciences 8
Boc-Gln-Otbu Boc-Gln-Otbu. Alternative Names: Boc-L-Gln-OtBu; N2-Boc-L-glutamine tert-butyl ester; L-Glutamine, N2-[(1,1-dimethylethoxy)carbonyl]-, 1,1-dimethylethyl ester. CAS No. 295325-99-4. Molecular formula: C14H26N2O5. Mole weight: 302.37. BOC Sciences 8
BOC-GLU-LYS-LYS-MCA BOC-GLU-LYS-LYS-MCA is a sensitive fluorogenic substrate for urokinase-activated plasmin. Alternative Names: T-BUTYLOXYCARBONYL-L-GLUTAMYL-L-LYSYL-L-LYSINE 4-METHYLCOUMARYL-7-AMIDE; BOC-GLU-LYS-LYS-AMC ACETATE SALT; BOC-GLU-LYS-LYS-AMC ACOH; BOC-GLU-LYS-LYS-MCA; Boc-Glu-Lys-Lys-AMC; N-T-boc-glu-lys-lys 7-amido-4-*methylcoumarin; N-tert-BOC-Glu-Lys 7-amido-4-methylcou. Grades: ≥97%. CAS No. 73554-85-5. Molecular formula: C32H48N6O9. Mole weight: 660.76. BOC Sciences 8
BOC-GLU(OBZL)-ALA-ARG-AMC HCL A fluorogenic substrate for coagulation factor XIa and trypsin. Alternative Names: N-BOC-gamma-benzyl-Glu-Ala-Arg-7-amido-4-methylcoumarin HCl; Boc-γ-benzyl-Glu-Ala-Arg-7-amido-4-methylcoumarin hydrochloride. Grades: 95%. CAS No. 133448-25-6. Molecular formula: C36H48ClN7O9. Mole weight: 758.26. BOC Sciences 8
Boc-Glu-Obzl DCHA Boc-Glu-Obzl DCHA. Alternative Names: Dicyclohexylamine (4S)-4-[(2-methylpropan-2-yl)oxycarbonylamino]-5-oxo-5-phenylmethoxypentanoic acid. CAS No. 30924-91-5. Molecular formula: C17H23NO6·C12H23N. Mole weight: 518.4. BOC Sciences 8
Boc-Glu(OBzl)-Gly-Arg-AMC HCl Substrate for coagulation factors IXa and XIIa as well as for trypsin and soybean trypsin-like enzyme. Alternative Names: benzyl (4S)-5-[[2-[[(2S)-5-(diaminomethylideneamino)-1-[(4-methyl-2-oxochromen-7-yl)amino]-1-oxopentan-2-yl]amino]-2-oxoethyl]amino]-4-[(2-methylpropan-2-yl)oxycarbonylamino]-5-oxopentanoate hydrochloride. Grades: ≥ 96% (HPLC). CAS No. 133448-22-3. Molecular formula: C35H45N7O9·HCl. Mole weight: 744.24. BOC Sciences 8
Boc-Glu(OBzl)-OH DCHA Boc-Glu(OBzl)-OH DCHA. Alternative Names: Boc-Glu(OBn)-OH.DCHA; N-tert-butoxycarbonyl-O5-benzyl-L-glutamic acid dicyclohexylamine; Dicyclohexylamine (S)-5-(benzyloxy)-2-((tert-butoxycarbonyl)amino)-5-oxopentanoate; Boc-Glu(OBzl)-OH (dicyclohexylammonium) salt; (2S)-5-(Benzyloxy)-2-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-5-oxopentanoic acid N-cyclohexylcyclohexanamine (1:1); L-Glutamic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 5-(phenylmethyl) ester, compd. with N-cyclohexylcyclohexanamine (1:1); Boc-L-glutamic acid 5-benzyl ester (dicyclohexylammonium) salt. Grades: ≥95%. CAS No. 13574-84-0. Molecular formula: C29H46N2O6. Mole weight: 518.69. BOC Sciences 8
Boc-Glu-OEt DCHA Boc-Glu-OEt DCHA. Alternative Names: N-α-(t-Butoxycarbonyl)-L-glutamic acid dicyclohexylammonium salt; Dicyclohexylamine (4S)-5-ethoxy-4-[(2-methylpropan-2-yl)oxycarbonylamino]-5-oxopentanoic acid. Molecular formula: C24H44N2O6. Mole weight: 456.62. BOC Sciences 8
Boc-Glu(OtBu)-ONp Boc-Glu(OtBu)-ONp. Alternative Names: BOC-GLU(OTBU)-ONP; BOC-L-GLUTAMIC ACID Y-T-BUTYL A-P-NITROPHENYL-DIESTER. Grades: ≥ 95%. CAS No. 69876-58-0. Molecular formula: C20H28N2O8. Mole weight: 424.45. BOC Sciences 8
Boc-Glu(Pip)-OH Boc-Glu(Pip)-OH. CAS No. 116596-43-1. Molecular formula: C15H26N2O5. Mole weight: 314.38. BOC Sciences 8
Boc-Glutaminol(OBzl) Boc-Glutaminol(OBzl). Molecular formula: C17H25NO5. Mole weight: 323.4. BOC Sciences 8
Boc-glycine 4-nitrophenyl ester A substrate for chymotrypsin and trypsin. Alternative Names: Boc-Gly-Onp; 4-nitrophenyl n-(tert-butoxycarbonyl)glycinate; 4-Nitrophenyl N-((1,1-dimethylethoxy)carbonyl)glycinate. Grades: ≥ 98% (TLC). CAS No. 3655-5-8. Molecular formula: C13H16N2O6. Mole weight: 296.30. BOC Sciences 8
Boc-glycine cesium salt Boc-glycine cesium salt. Alternative Names: Boc-Gly-OCs salt; Cesium 2-((tert-butoxycarbonyl)amino)acetate. Grades: ≥ 98% (HPLC). CAS No. 42538-64-7. Molecular formula: C7H12NO4Cs. Mole weight: 307.09. BOC Sciences 8
Boc-glycine methyl ester Boc-glycine methyl ester. Alternative Names: Boc-Gly-Ome; Methyl 2-[(tert-butoxycarbonyl)amino]acetate. Grades: ≥ 98% (GC). CAS No. 31954-27-5. Molecular formula: C8H15NO4. Mole weight: 189.21. BOC Sciences 8
Boc-glycine N-hydroxysuccinimide ester Boc-glycine N-hydroxysuccinimide ester. Alternative Names: Boc-Gly-OSu. Grades: ≥ 99% (HPLC). CAS No. 3392-7-2. Molecular formula: C11H16N2O6. Mole weight: 272.30. BOC Sciences 8
Boc-glycine tert-butyl ester Boc-glycine tert-butyl ester. Alternative Names: Boc-Gly-OtBu; tert-Butyl 2-((tert-butoxycarbonyl)amino)acetate. Grades: ≥ 98% (HPLC). CAS No. 111652-20-1. Molecular formula: C11H21NO4. Mole weight: 231.29. BOC Sciences 8
Boc-Glycinol A reagent used in the synthesis of phosphatidyl ethanolamines and ornithine. Alternative Names: 2-(Boc-amino)-ethanol; Boc-ethanolamine; N-Boc-ethanolamine; tert-Butyl N-(2-hydroxyethyl)carbamate; tert-butyl (2-hydroxyethyl)carbamate. Grades: ≥ 97 % (Assay). CAS No. 26690-80-2. Molecular formula: C7H15NO3. Mole weight: 161.2. BOC Sciences 8
Boc-Gly-Gly-Gly-OH Boc-Gly-Gly-Gly-OH. Alternative Names: Nα-τ-Butoxycarbonyl-glycyl-glycyl-glycine; Boc-(Gly)3-OH. Grades: ≥ 99% (HPLC). CAS No. 28320-73-2. Molecular formula: C11H19N3O6. Mole weight: 289.29. BOC Sciences 8
Boc-Gly-Gly-OH Boc-Gly-Gly-OH. Alternative Names: N-(2-N-Boc-aminoacetyl)glycine. Grades: ≥ 98% (HPLC). CAS No. 31972-52-8. Molecular formula: C9H16N2O5. Mole weight: 232.24. BOC Sciences 8
Boc-Gly-Gly-OSu Boc-Gly-Gly-OSu. Alternative Names: 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 Sciences 8
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). Alternative Names: 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. Grades: >95%. CAS No. 187794-49-6. Molecular formula: C20H28N4O7. Mole weight: 436.46. BOC Sciences 8
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). Alternative Names: Boc-Gly-Gly-Phe-Gly-OH trifluoroacetic acid; N-tert-butoxycarbonyl-glycyl-glycyl-L-phenylalanyl-glycine trifluoroacetic acid. Grades: >98%. Molecular formula: C22H29F3N4O9. Mole weight: 550.48. BOC Sciences 8
Boc-Gly-Gly-Tyr-OH Boc-Gly-Gly-Tyr-OH. Molecular formula: C18H25N3O7. Mole weight: 395.4. BOC Sciences 8
Boc-Gly-Leu-OH Boc-Gly-Leu-OH. Alternative Names: (2S)-4-methyl-2-[[2-[(2-methylpropan-2-yl)oxycarbonylamino]acetyl]amino]pentanoic acid. Grades: ≥ 95%. CAS No. 51871-42-2. Molecular formula: C13H24N2O5. Mole weight: 288.30. BOC Sciences 8
Boc-Gly-Oipr Boc-Gly-Oipr. Alternative Names: 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 Sciences 8
Boc-Gly-Tyr-Ome Boc-Gly-Tyr-Ome. CAS No. 65160-62-5. Molecular formula: C17H24N2O6. Mole weight: 352.38. BOC Sciences 8
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. Alternative Names: 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. Grades: 95%. CAS No. 113866-14-1. Molecular formula: C29H44N10O7. Mole weight: 644.72. BOC Sciences 8
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. Grades: 98%. Molecular formula: C29H44N10O7.xC2HF3O2. Mole weight: 644.72 (free base). BOC Sciences 8
Boc-His(1-Me)-OH Boc-His(1-Me)-OH. Alternative Names: Boc-L-His(Nim-Me)-OH; Boc-His(τ-Me)-OH. Grades: ≥ 99% (HPLC). CAS No. 61070-20-0. Molecular formula: C12H19N3O4. Mole weight: 269.30. BOC Sciences 8
Boc-His(3-Bom)-OH Boc-His(3-Bom)-OH. Alternative Names: Boc-L-His(p-Bom)-OH; Boc-N-p-benzyloxymethyl-L-histidine; Nalpha-Boc-3-[(benzyloxy)methyl]-L-histidine. Grades: ≥ 98.5% (HPLC). CAS No. 79950-65-5. Molecular formula: C19H25N3O5. Mole weight: 375.43. BOC Sciences 8
Boc-His(3-Me)-OH Boc-His(3-Me)-OH. Alternative Names: Boc-L-His(p-Me)-OH; Boc-N-p-methyl-L-histidine; (S)-2-(Boc-amino)-3-(1-methyl-5-imidazolyl)propanoic Acid. Grades: ≥ 99% (HPLC). CAS No. 61070-22-2. Molecular formula: C12H19N3O4. Mole weight: 269.30. BOC Sciences 8
Boc-His(Boc)-OH Benzene Boc-His(Boc)-OH Benzene. Alternative Names: 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 Sciences 8
Boc-His(Boc)-OMe Boc-His(Boc)-OMe. Alternative Names: 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 Sciences 8
Boc-His(Dnp)-OH IPA Boc-His(Dnp)-OH IPA. Alternative Names: 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 Sciences 8
Boc-His(Fmoc)-OH Boc-His(Fmoc)-OH. Molecular formula: C26H27N3O6. Mole weight: 477.5. BOC Sciences 8
Boc-His-Gly-OH Boc-His-Gly-OH. Alternative Names: 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 Sciences 8
Boc-His-Met-OH Boc-His-Met-OH. Grades: ≥ 98%. CAS No. 248921-84-8. Molecular formula: C16H26N4O5S. Mole weight: 386.47. BOC Sciences 8
Boc-His(Mts)-aldehyde Boc-His(Mts)-aldehyde. Alternative Names: 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 Sciences 8
Boc-Histidinol(Tos) Boc-Histidinol(Tos). Alternative Names: Boc-His(1-Tos)-ol. CAS No. 1169760-85-3. Molecular formula: C18H25N3O5S. Mole weight: 395.5. BOC Sciences 8
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. Alternative Names: HXQGG; N2-(2-((S)-2-((tert-Butoxycarbonyl)amino)-3-(1-trityl-1H-imidazol-4-yl)propanamido)-2-methylpropanoyl)-N5-trityl-L-glutaminylglycylglycine. Grades: ≥96%. Molecular formula: C62H66N8O9. Mole weight: 1067.26. BOC Sciences 8
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. Alternative Names: HXQ; N2-(2-((S)-2-((tert-Butoxycarbonyl)amino)-3-(1-trityl-1H-imidazol-4-yl)propanamido)-2-methylpropanoyl)-N5-trityl-L-glutamine. Grades: ≥95%. Molecular formula: C58H60N6O7. Mole weight: 953.15. BOC Sciences 8
Boc-His(Trt)-Aib-Glu(OBtu)-Gly-OH Boc-His(Trt)-Aib-Glu(OBtu)-Gly-OH. Alternative Names: ((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 Sciences 8
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. Alternative Names: HXG; (S)-(2-(2-((tert-Butoxycarbonyl)amino)-3-(1-trityl-1H-imidazol-4-yl)propanamido)-2-methylpropanoyl)glycine. Grades: ≥97%. Molecular formula: C36H41N5O6. Mole weight: 639.75. BOC Sciences 8
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. Alternative Names: HQG; N2-(Na-(tert-Butoxycarbonyl)-Nt-trityl-L-histidyl)-N5-trityl-L-glutaminylglycine. Grades: ≥96%. Molecular formula: C56H56N6O7. Mole weight: 925.10. BOC Sciences 8

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