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Protective agent of peptide synthesis. Synonyms: TIPS. Grades: ≥ 99% (GC). CAS No. 6485-79-6. Molecular formula: C9H22Si. Mole weight: 158.36.
Triisopropylsilane
Triisopropylsilane. Group: Biochemicals. Grades: Highly Purified. CAS No. 6485-79-6. Pack Sizes: 100g, 200g, 300g, 500g, 1kg. Molecular Formula: C9H22Si. US Biological Life Sciences.
Worldwide
Triisopropylsilane
Triisopropylsilane. Group: Salt. Alternative Names: TIS. CAS No. 6485-79-6. Pack Sizes: 10 g; 100 g. Product ID: tri(propan-2-yl)silicon. Molecular formula: 158.36. Mole weight: C9H22Si. CC(C)[Si](C(C)C)C(C)C. ZGYICYBLPGRURT-UHFFFAOYSA-N. 98%.
Triisopropylsilane, 98%
Triisopropylsilane, 98% is a strong reducing agent. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: TIS, 98%. CAS No. 6485-79-6. Pack Sizes: 25 g. Product ID: HY-Y1410.
Triisopropylsilane 99+% (GC)
Triisopropylsilane 99+% (GC). Group: Biochemicals. Grades: GC. CAS No. 6485-79-6. Pack Sizes: 5g, 25g, 100g, 250g, 1Kg. US Biological Life Sciences.
Worldwide
(2- (3-Bromophenyl) propoxy) triisopropylsilane
(2- (3-Bromophenyl) propoxy) triisopropylsilane is an intermediate in the synthesis of Ketoprofen (K200800) related compounds. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg, 25mg. Molecular Formula: C18H31BrOSi. US Biological Life Sciences.
Worldwide
(Bromoethynyl)Triisopropylsilane
OrganosiliconeSilane Compound. CAS No. 111409-79-1. Molecular formula: C11H21BrSi. Mole weight: 261.27 g/mol. Appearance: Colorless to Red to Green clear liquid. Purity: ≥95%. Catalog: ACM111409791.
Chloro-(2'-chloro)trityl Polystyrene, Type1
A very acid-sensitive resin is suitable for the synthesis of protected peptide fragments by the Fmoc strategy. In particular suitable for the preparation of C-terminal prolyl and cysteinyl peptides. Cleavage from this resin is achieved by using 1-95% TFA in CH2Cl2 (containing 8% triisopropylsilane), AcOH/CF3OH/CH2Cl2, 0.5% TFA or hexafluoroisopropanol. Uses: Recently, this resin has been used in cyclization reactions under heck reaction conditions, the solid phase synthesis of b-peptides via the arndt-eistert homologation of fmoc-protected amino acid diazoketones and in mannich reactions of alkynes, secondary amines and aldehydes in the presence of a copper (I) salt leading to the corresponding aminomethylalkynyl adducts. this resin can also be used in fmoc peptide synthesis. carboxylic acids can be released under very mild acidic conditions by treatment with acoh/tfe/dcm or hfip in dcm. completely protected peptides are generated under these conditions. Group: Chloro-(2-chloro)trityl polystyrene resins. Pack Sizes: 5g, 25g, 100g.
Chloro-(2'-chloro)trityl Polystyrene, Type2
A very acid-sensitive resin is suitable for the synthesis of protected peptide fragments by the Fmoc strategy. In particular suitable for the preparation of C-terminal prolyl and cysteinyl peptides. Cleavage from this resin is achieved by using 1-95% TFA in CH2Cl2 (containing 8% triisopropylsilane), AcOH/CF3OH/CH2Cl2, 0.5% TFA or hexafluoroisopropanol. Uses: Recently, this resin has been used in cyclization reactions under heck reaction conditions, the solid phase synthesis of b-peptides via the arndt-eistert homologation of fmoc-protected amino acid diazoketones and in mannich reactions of alkynes, secondary amines and aldehydes in the presence of a copper (I) salt leading to the corresponding aminomethylalkynyl adducts. this resin can also be used in fmoc peptide synthesis. carboxylic acids can be released under very mild acidic conditions by treatment with acoh/tfe/dcm or hfip in dcm. completely protected peptides are generated under these conditions. Group: Chloro-(2-chloro)trityl polystyrene resins. Pack Sizes: 5g, 25g, 100g.
Chloro-(2'-chloro)trityl Polystyrene, Type3
A very acid-sensitive resin is suitable for the synthesis of protected peptide fragments by the Fmoc strategy. In particular suitable for the preparation of C-terminal prolyl and cysteinyl peptides. Cleavage from this resin is achieved by using 1-95% TFA in CH2Cl2 (containing 8% triisopropylsilane), AcOH/CF3OH/CH2Cl2, 0.5% TFA or hexafluoroisopropanol. Uses: Recently, this resin has been used in cyclization reactions under heck reaction conditions, the solid phase synthesis of b-peptides via the arndt-eistert homologation of fmoc-protected amino acid diazoketones and in mannich reactions of alkynes, secondary amines and aldehydes in the presence of a copper (I) salt leading to the corresponding aminomethylalkynyl adducts. this resin can also be used in fmoc peptide synthesis. carboxylic acids can be released under very mild acidic conditions by treatment with acoh/tfe/dcm or hfip in dcm. completely protected peptides are generated under these conditions. Group: Chloro-(2-chloro)trityl polystyrene resins. Pack Sizes: 5g, 25g, 100g.
Chlorotrityl Polystyrene, Type1
Chlorotrityl Polystyrene, Type1. Uses: This highly acid labile resin is useful for the immobilization of alcohols, amines and carboxylic acids. cleavage is in general achieved by using either 1-5% tfa in ch2cl2 (containing 5% triisopropylsilane) or acetic acid. this resin can also be used in fmoc peptide synthesis under basic acylation conditions. carboxylic acids can be released under very mild acidic conditions by treatment with acoh/tfe/dcm or hfip in dcm. completely protected peptides are generated under this conditions. Group: Chlorotrityl polystyrene resins. Alternative Names: Trityl Chloride Resin. Pack Sizes: 5g, 25g, 100g.
Chlorotrityl Polystyrene, Type2
Chlorotrityl Polystyrene, Type2. Uses: This highly acid labile resin is useful for the immobilization of alcohols, amines and carboxylic acids. cleavage is in general achieved by using either 1-5% tfa in ch2cl2 (containing 5% triisopropylsilane) or acetic acid. this resin can also be used in fmoc peptide synthesis under basic acylation conditions. carboxylic acids can be released under very mild acidic conditions by treatment with acoh/tfe/dcm or hfip in dcm. completely protected peptides are generated under this conditions. Group: Chlorotrityl polystyrene resins. Alternative Names: Trityl Chloride Resin. Pack Sizes: 5g, 25g, 100g.
Chlorotrityl Polystyrene, Type3
Chlorotrityl Polystyrene, Type3. Uses: This highly acid labile resin is useful for the immobilization of alcohols, amines and carboxylic acids. cleavage is in general achieved by using either 1-5% tfa in ch2cl2 (containing 5% triisopropylsilane) or acetic acid. this resin can also be used in fmoc peptide synthesis under basic acylation conditions. carboxylic acids can be released under very mild acidic conditions by treatment with acoh/tfe/dcm or hfip in dcm. completely protected peptides are generated under this conditions. Group: Chlorotrityl polystyrene resins. Alternative Names: Trityl Chloride Resin. Pack Sizes: 5g, 25g, 100g.
Fmoc-O-trityl-D-threonine
Side-chain can be selectively deprotected on the solid phase with 1% TFA/5% triisopropylsilane. Synonyms: Fmoc-D-Thr(Trt)-OH; Fmoc-D-Thr(OTrt)-OH. Grades: ≥ 98% (HPLC). CAS No. 682800-84-6. Molecular formula: C38H33NO5. Mole weight: 583.70.