You Searched For: trans-4-Methoxycyclohexan-1-amine


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Supplier: Apollo Scientific
Description: trans-4-Methoxycyclohexan-1-amine 95%

Catalog Number: (APOSOR916743-1G)
Supplier: Apollo Scientific
Description: 2-(4-Methoxycyclohexyl)ethylamine (cis- and trans- mixture) 95%
UOM: 1 * 1 g


Catalog Number: (APOSOR917041-5G)
Supplier: Apollo Scientific
Description: Methoxycyclohexane 95%
UOM: 1 * 5 g


Supplier: Apollo Scientific
Description: [[4-(Trifluoromethyl)cyclohexyl]methyl]amine(cis- and trans- mixture) 97%

Supplier: Apollo Scientific
Description: trans-4-Methylcyclohexylamine

Supplier: Apollo Scientific
Description: 4-Ethylcyclohexylamine (cis- and trans- mixture) 95%

Supplier: Thermo Fisher Scientific
Description: trans-N-(6,6-Dimethyl-2-hepten-4-ynyl)-N-methyl-1-naphthylmethylamine hydrochloride 99%

Supplier: Thermo Fisher Scientific
Description: Naftifine hydrochloride 99%

Catalog Number: (ENZOBMLEI3180100)
Supplier: ENZO LIFE SCIENCES
Description: Inhibits ergosterol biosynthesis at the level of squalene epoxidase. Potent non-competitive inhibitor of squalene epoxidase from Candida (Ki=30 nM), inhibiting mammalian enzymes at higher concentrations (4-77 µM). It inhibits HUVEC proliferation and angiogenesis and displays interesting anti-inflammatory and free radical scavenging activities. Clinically useful antifungal agent.
UOM: 1 * 100 mg

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Supplier: Apollo Scientific
Description: Primary amine and Sulphhydryl reactive, Enzyme antibody conjugation.

Catalog Number: (APOSBICL207-100MG)
Supplier: Apollo Scientific
Description: Primary amine & Sulphhydryl reactiveEnzyme-antibody conjugation -Stable maleimide groupRef: Hushida, S. et al (1984) J.Applied Biochem. 56,56-63
UOM: 1 * 100 mg


Catalog Number: (PRSI91-195)
Supplier: ProSci Inc.
Description: Cyclophilin C is an enzyme (EC 5.2.1.8) found in both prokaryotes and eukaryotes that interconverts the cis and trans isomers of peptide bonds with the amino acid proline. Proline has an unusually conformationally restrained peptide bond due to its cyclic structure with its side chain bonded to its secondary amine nitrogen. Most amino acids have a strong energetic preference for the trans peptide bond conformation due to steric hindrance, but prolines unusual structure stabilizes the cis form so that both isomers are populated under biologically relevant conditions. Proteins with prolyl isomerase activity include cyclophilin, FKBPs, and parvulin, although larger proteins can also contain prolyl isomerase domains.
UOM: 1 * 50 µG


Supplier: Thermo Fisher Scientific
Description: Thermo Scientific Pierce Premium Grade Sulfo-SMCC is our highest quality formulation of amine-to-sulfhydryl crosslinker, specially characterized for applications where product integrity and risk minimization are paramount.

Supplier: Thermo Fisher Scientific
Description: Thermo Scientific Pierce Sulfo-SMCC, No-Weigh Format is a water-soluble, amine-to-sulfhydryl crosslinker that contains NHS-ester and maleimide reactive groups at opposite ends of a medium-length cyclohexane spacer arm (8.3 angstroms).

Catalog Number: (PIERA39268)
Supplier: Thermo Fisher Scientific
Description: Thermo Scientific Pierce Sulfo-SMCC, No-Weigh Format is a water-soluble, amine-to-sulfhydryl crosslinker that contains NHS-ester and maleimide reactive groups at opposite ends of a medium-length cyclohexane spacer arm (8.3 angstroms).
UOM: 1 * 20 mg


Catalog Number: (PIERA35394)
Supplier: Thermo Fisher Scientific
Description: Thermo Scientific Pierce SMCC is a hetero-bifunctional crosslinker that contain N-hydroxysuccinimide (NHS) ester and maleimide groups that allow covalent conjugation of amine- and sulfhydryl-containing molecules. NHS esters react with primary amines at pH 7–9 to form amide bonds, while maleimides react with sulfhydryl groups at pH 6.5–7.5 to form stable thioether bonds. In aqueous solutions, NHS ester hydrolytic degradation is a competing reaction whose rate increases with pH. The maleimide group is more stable than the NHS-ester group, but will slowly hydrolyze and lose its reaction specificity for sulfhydryls at pH values > 7.5. For these reasons, conjugations with these crosslinkers are usually performed at pH 7.2–7.5, with the NHS ester (amine-targeted) reacted before or simultaneous with the maleimide (sulfhydryl-targeted) reaction.
UOM: 1 * 10 mg


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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at +43 1 97002 - 0.
Dual use goods can only be delivered within the European Union.
Dual use goods can only be delivered within the European Union.
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The original product is no longer available. The replacement shown is available.
This product is no longer available. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service at +43 1 97002 - 0.
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