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733776-8INFeatures and Benefits 31 P sensitivity Quantity 10 mm O.D.
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8082700005Analysis Note Assay (GC, area%): ≥ 99.0 % (a/a) Melting range (lower value): ≥ 79 °C Melting range (upper value): ≤ 82 °C Identity (IR): passes test
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8082700250Analysis Note Assay (GC, area%): ≥ 99.0 % (a/a) Melting range (lower value): ≥ 79 °C Melting range (upper value): ≤ 82 °C Identity (IR): passes test
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8082701000Analysis Note Assay (GC, area%): ≥ 99.0 % (a/a) Melting range (lower value): ≥ 79 °C Melting range (upper value): ≤ 82 °C Identity (IR): passes test
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8082709025
Sigma-Aldrich
TRIPHENYLPHOSPHINE FOR SYNTHESIS (C15-1251-661)
Price: $3,461.54List Price: $3,846.15Analysis Note Assay (GC, area%): ≥ 99.0 % (a/a) Melting range (lower value): ≥ 79 °C Melting range (upper value): ≤ 82 °C Identity (IR): passes test -
775444-2.5GApplication Monodentate P-donor ligand. Used as a phosphitylation reagent for oligonucleotide synthesis.
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775444-500MGApplication Monodentate P-donor ligand. Used as a phosphitylation reagent for oligonucleotide synthesis.
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392081-5GApplication Highly basic arylphosphine.
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395080-1G
Sigma-Aldrich
Tris(2,4,6-trimethylphenyl)phosphine (C15-1224-984)
Price: $187.29List Price: $208.10Tris(2,4,6-trimethylphenyl)phosphine -
395080-5G
Sigma-Aldrich
Tris(2,4,6-trimethylphenyl)phosphine (C15-1224-985)
Price: $415.29List Price: $461.43Tris(2,4,6-trimethylphenyl)phosphine -
52486-1ML
Sigma-Aldrich
Tris(2-carboxyethyl)phosphine, immobilized on Agarose CL-4B (C15-1304-858)
Price: $315.92List Price: $351.02Application Tris(2-carboxyethyl)phosphine, immobilized on agarose CL-4B may be used in preliminary off-line experiments to study its ability to cleave disulfide bonds by both under flow conditions using sequential injection analysis (SI). It may -
52486-5ML
Sigma-Aldrich
Tris(2-carboxyethyl)phosphine, immobilized on Agarose CL-4B (C15-1304-859)
Price: $1,148.57List Price: $1,276.19Application Tris(2-carboxyethyl)phosphine, immobilized on agarose CL-4B may be used in preliminary off-line experiments to study its ability to cleave disulfide bonds by both under flow conditions using sequential injection analysis (SI). It may