333 Results for: "3-Hydroxy-1-adamantane carboxylic acid&"
trans-4-Hydroxy-L(-)-proline
Supplier: PanReac AppliChem
trans-4-Hydroxy-L(-)-proline
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trans-4-Hydroxy-L(-)-proline
Supplier: Apollo Scientific
trans-4-Hydroxy-L(-)-proline
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D-(-)-Luciferin potassium salt
Supplier: Apollo Scientific
D-(-)-Luciferin potassium salt
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Cromolyn disodium salt hydrate ≥98.0% (by HPLC, titration analysis)
Supplier: TCI
Cromolyn disodium salt hydrate ≥98.0% (by HPLC, titration analysis)
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(2S,4R)-Methyl-4-hydroxypyrrolidine-2-carboxylate hydrochloride ≥98.0% (by titrimetric analysis)
Supplier: TCI
(2S,4R)-Methyl-4-hydroxypyrrolidine-2-carboxylate hydrochloride ≥98.0% (by titrimetric analysis)
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trans-4-Hydroxy-L(-)-proline 99+%
Supplier: Thermo Fisher Scientific
trans-4-Hydroxy-L(-)-proline 99+%
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3-Hydroxypicolinic acid ≥98%
Supplier: Thermo Fisher Scientific
3-Hydroxypicolinic acid ≥98%
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trans-4-Hydroxy-L(-)-proline ≥99%
Supplier: Thermo Fisher Scientific
trans-4-Hydroxy-L(-)-proline ≥99%
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Vindoline ≥90% (dry basis)
Supplier: ENZO LIFE SCIENCES
Vindoline ≥90% (dry basis)
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trans-4-Hydroxy-L(-)-proline ≥99.0% (by HPLC, titration analysis)
Supplier: TCI
trans-4-Hydroxy-L(-)-proline ≥99.0% (by HPLC, titration analysis)
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Flurenol (9-hydroxy-9H-fluorene-9-carboxylic acid)
Supplier: EHRENSTORFER
Flurenol (9-hydroxy-9H-fluorene-9-carboxylic acid)
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Chloroflurenol (2-Chloro-9-hydroxy-9H-fluorene-9-carboxylic acid)
Supplier: EHRENSTORFER
Chloroflurenol(2-chloro-9-hydroxy-9H-fluorene-9-carboxylic acid)
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Lovastatin hydroxy acid sodium ≥97% (by HPLC)
Supplier: ENZO LIFE SCIENCES
Active carboxylate form of Lovastatin. Active in whole cells as well as cell-free assays. Inhibits cholesterol/ isoprenoid biosynthesis by inhibition of HMG-CoA reductase (Ki for acid form is 1 nM) and blocks protein isoprenylation and reduces plasma cholesterol levels in humans. Causes cells to arrest early in the G1 phase.
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cis-4-Hydroxy-D(+)-proline ≥98%
Supplier: Thermo Fisher Scientific
cis-4-Hydroxy-D(+)-proline ≥98%
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Flurenol (9-hydroxy-9H-fluorene-9-carboxylic acid)
Supplier: Molekula
Flurenol (9-hydroxy-9H-fluorene-9-carboxylic acid)
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cis-4-Hydroxy-D(+)-proline 98%
Supplier: Apollo Scientific
cis-4-Hydroxy-D(+)-proline 98%
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cis-4-Hydroxy-D(+)-proline 99%
Supplier: Thermo Fisher Scientific
cis-4-Hydroxy-D(+)-proline 99%
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Flurenol-butyl ester (9-Hydroxy-9H-fluorene-9-carboxylic acid butyl ester)
Supplier: EHRENSTORFER
Flurenol butyl ester (9-hydroxy-9H-fluorene-9-carboxylic acid butyl ester)
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Chlorflurenol-methyl ester (2-Chloro-9-hydroxy-9H-fluorene-9-carboxylic acid methyl ester)
Supplier: EHRENSTORFER
Chlorflurenolmethyl ester(2-chloro-9-hydroxy-9H-fluorene-9-carboxylic acid methyl ester)
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cis-4-Hydroxy-D(+)-proline ≥98.0% (by HPLC, titration analysis)
Supplier: TCI
cis-4-Hydroxy-D(+)-proline ≥98.0% (by HPLC, titration analysis)
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Sulpho-NHS (N-Hydroxysulphosuccinimide sodium salt)
Supplier: G-Biosciences
Sulpho-NHS reacts primarily with primary amines to convert carboxyl groups to amine reactive sulfo-NHS esters. It is ideal for cross-linking, chemical labelling and solid support immobilisation. It is used to generate amine reactive esters from carboxylate groups and is primarily used to increase the efficiency of the carbodiimide EDC cross-linking. EDC reactions do not require Sulpho-NHS; however, its presence greatly enhances cross-linking efficiency and allows for a two-step process. EDC reacts with a carboxylate group to form an active ester, which is subject to rapid hydrolysis in aqueous buffers. The Sulfo-NHS increases the stability of the active intermediate and the resulting coupled product is identical to EDC reactions without sulpho-NHS.
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Patton-Reeders reagent (Calconcarboxylic acid) for complexometry, Fluka™
Supplier: Honeywell Chemicals
Patton-Reeders reagent (Calconcarboxylic acid) for complexometry, Fluka™
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N-Succinimidyl 7-Hydroxycoumarin-3-carboxylate ≥90%
Supplier: AAT BIOQUEST
7-Hydroxycoumarin-3-carboxylic acid, SE is the amine-reactive succinimidyl ester of 7-Hydroxycoumarin-3-carboxylic acid.
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7-Hydroxycoumarin-3-carboxylic acid ≥90%
Supplier: AAT BIOQUEST
7-Hydroxycoumarin-3-carboxylic acid is a blue fluorophores for labeling proteins and nucleic acids mostly through the in situ formation of its succinimidyl ester catalyzed by EDAC.
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Organic reference standards, fosinoprils, Ph. Eur.
Supplier: EDQM
Organic Standard, Fosinopril impurity A, (2S,4S)-4-cyclohexyl-1-[[(R)-hydroxy(4-phenylbutyl)phosphoryl]acetyl]pyrrolidine-2-carboxylic acid, Ph. Eur. standard