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Boc-D-proline N-hydroxysuccinimide ester 98+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 10g. US Biological Life Sciences.
Worldwide
Boc-D-prolinol
N-Boc-D-prolinol (CAS# 83435-58-9) is used to prepare (azetidinyl)methoxy]pyridines and 2-(aryloxymethyl) azacyclic analogs with therapeutic potetials for the treatment of central nervous system (CNS) disorders. Synonyms: Boc-D-Pro-ol; N-tert-butoxycarbonyl-D-prolinol; N-Boc-D-prolinol; (R)-tert-butyl 2-(hydroxymethyl)pyrrolidine-1-carboxylate; (R)-(+)-1-Boc-2-pyrrolidinemethanol; 1-Boc-D-Prolinol; (R)-(+)-1-(tert-Butoxycarbonyl)-2-pyrrolidinemethanol; N-t-Boc-D-prolinol; 1-Pyrrolidinecarboxylic acid, 2-(hydroxymethyl)-, 1,1-dimethylethyl ester, (2R)-. Grade: ≥95%. CAS No. 83435-58-9. Molecular formula: C10H19NO3. Mole weight: 201.26.
Boc-D-Prolinol 98+% (HPLC)
Boc-D-Prolinol 98+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. CAS No. 83435-58-9. Pack Sizes: 1g, 5g, 25g, 100g, 250g. US Biological Life Sciences.
Worldwide
Boc-D-Propargylglycine
Boc-D-Propargylglycine. Group: Biochemicals. Grades: Highly Purified. CAS No. 63039-46-3. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. US Biological Life Sciences.
Worldwide
Boc-D-Propargylglycine
Boc-D-Propargylglycine. CAS No: 63039-46-3
Sarchem Laboratories New Jersey NJ
Boc-D-propraglycine dicyclohexylammonium salt
Boc-D-propraglycine dicyclohexylammonium salt. Group: Biochemicals. Alternative Names: Boc-D-propragyl-Gly-OH·DCHA; Boc-D-Pra-OH·DCHA; (R)-2-(Boc-amino)-4-pentynoic acid dicyclohexylamine salt. Grades: Highly Purified. CAS No. 63039-47-4. Pack Sizes: 500mg, 1g, 2g, 5g. US Biological Life Sciences.
Worldwide
Boc-D-propraglycine dicyclohexylammonium salt
Boc-D-propraglycine dicyclohexylammonium salt. Synonyms: Boc-D-propragyl-Gly-OH DCHA; Boc-D-Pra-OH DCHA; (R)-2-(Boc-amino)-4-pentynoic acid dicyclohexylamine salt; Boc D Pra OH DCHA. Grade: ≥ 98% (HPLC). CAS No. 63039-47-4. Molecular formula: C10H15NO4·C12H23N. Mole weight: 394.55.
Boc-D-propraglycine dicyclohexylammonium salt 99+%
Boc-D-propraglycine dicyclohexylammonium salt 99+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 250mg, 1g, 5g. US Biological Life Sciences.
Boc-D-trans-Hyp-OH is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). It is also an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs. Synonyms: (2R,4S)-1-(tert-butoxycarbonyl)-4-hydroxypyrrolidine-2-carboxylic acid; N-Boc-trans-4-hydroxy-d-proline. Grade: ≥ 97%. CAS No. 147266-92-0. Molecular formula: C10H17NO5. Mole weight: 231.25.
Boc-D-trans-Hyp-Ome
Boc-D-trans-Hyp-Ome is a non-cleavable ADC linker and also an alkyl chain-based PROTAC linker. Synonyms: (2R,4S)-1-tert-Butyl 2-methyl 4-hydroxypyrrolidine-1,2-dicarboxylate; 1-tert-butyl 2-methyl (2R,4S)-4-hydroxypyrrolidine-1,2-dicarboxylate; N-BOC-TRANS-4-HYDROXY-D-PROLINE METHYL ESTER. Grade: 98%. CAS No. 135042-17-0. Molecular formula: C11H19NO5. Mole weight: 245.27.
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. Synonyms: 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. Grade: ≥95%. Molecular formula: C48H59N5O9. Mole weight: 850.03.
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. Synonyms: 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. Grade: ≥90%. Molecular formula: C33H52N4O10. Mole weight: 664.80.
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. Synonyms: 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. Grade: ≥95%. Molecular formula: C22H34N2O6. Mole weight: 422.52.