3092 Results for: "3-Phenyl-N-prop-2-ynyl-indan-1-amine hydrochloride&"
3-Phenylpentan-3-amine hydrochloride 95%
Supplier: Apollo Scientific
3-Phenylpentan-3-amine hydrochloride 95%
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Cinacalcet hydrochloride
Supplier: Thermo Fisher Scientific
Cinacalcet hydrochloride
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Cinacalcet hydrochloride
Supplier: Apollo Scientific
Cinacalcet hydrochloride
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3-Amino-3'-(trifluoromethyl)biphenyl hydrochloride
Supplier: Apollo Scientific
3-Amino-3'-(trifluoromethyl)biphenyl hydrochloride
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4-Amino-4'-(trifluoromethyl)biphenyl hydrochloride
Supplier: Apollo Scientific
4-Amino-4'-(trifluoromethyl)biphenyl hydrochloride
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3-Amino-4'-(trifluoromethyl)biphenyl hydrochloride
Supplier: Apollo Scientific
3-Amino-4'-(trifluoromethyl)biphenyl hydrochloride
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4-Spiroindanepiperidine hydrochloride
Supplier: Apollo Scientific
4-Spiroindanepiperidine hydrochloride
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AMP (2-Amino-2-methylpropanol), high purity
Supplier: VWR Chemicals
5% water has been added to maintain liquidity at room temperature.
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3-Phenyl-o-anisidine hydrochloride
Supplier: FLUOROCHEM
3-Phenyl-o-anisidine hydrochloride
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N-(2-aminoethyl)prop-2-enamide hydrochloride
Supplier: Apollo Scientific
N-(2-aminoethyl)prop-2-enamide hydrochloride
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AMP (2-Amino-2-methylpropanol) for synthesis, Sigma-Aldrich®
Supplier: Merck
AMP (2-Amino-2-methylpropanol) for synthesis, Sigma-Aldrich®
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Ethyl 2-[1-(prop-2-ynylamino)ethyl]benzoate hydrochloride
Supplier: Apollo Scientific
Ethyl 2-[1-(prop-2-ynylamino)ethyl]benzoate hydrochloride
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Ethyl 4-[(1S)-1-(prop-2-ynylamino)ethyl]benzoate hydrochloride
Supplier: Apollo Scientific
Ethyl 4-[(1S)-1-(prop-2-ynylamino)ethyl]benzoate hydrochloride
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Ethyl 2-[(1S)-1-(prop-2-ynylamino)ethyl]benzoate hydrochloride
Supplier: Apollo Scientific
Ethyl 2-[(1S)-1-(prop-2-ynylamino)ethyl]benzoate hydrochloride
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1-(Prop-2-yn-1-yl)pyrrolidine hydrochloride 95%
Supplier: Apollo Scientific
1-(Prop-2-yn-1-yl)pyrrolidine hydrochloride 95%
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Ethyl 3-amino-3-[3-(trifluoromethyl)anilino]prop-2-en-1-oate hydrochloride
Supplier: Apollo Scientific
Ethyl 3-amino-3-[3-(trifluoromethyl)anilino]prop-2-en-1-oate hydrochloride
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EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride), Pierce™
Supplier: Thermo Fisher Scientific
Thermo Scientific Pierce EDC is a carboxyl- and amine-reactive zero-length crosslinker. EDC reacts with a carboxyl group first and forms an amine-reactive O-acylisourea intermediate that quickly reacts with an amino group to form an amide bond with release of an isourea by-product. The intermediate is unstable in aqueous solutions and so two-step conjugation procedures rely on N-hydroxysuccinimide (NHS) for stabilization. Failure to react with an amine will result in hydrolysis of the intermediate, regeneration of the carboxyl, and release of an N-substituted urea. A side reaction is the formation of an N-acylurea, which is usually restricted to carboxyls located in hydrophobic regions of proteins.
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Ethyl 3-[1-(prop-2-ynylamino)ethyl]benzoate hydrochloride
Supplier: Apollo Scientific
Ethyl 3-[1-(prop-2-ynylamino)ethyl]benzoate hydrochloride
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Ethyl 4-[1-(prop-2-ynylamino)ethyl]benzoate hydrochloride
Supplier: Apollo Scientific
Ethyl 4-[1-(prop-2-ynylamino)ethyl]benzoate hydrochloride
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AMP (2-Amino-2-methylpropanol) 99%
Supplier: Thermo Fisher Scientific
AMP (2-Amino-2-methylpropanol) 99%
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Ethyl 3-amino-3-[4-(trifluoromethoxy)anilino]prop-2-en-1-oate hydrochloride 97%
Supplier: Apollo Scientific
Ethyl 3-amino-3-[4-(trifluoromethoxy)anilino]prop-2-en-1-oate hydrochloride 97%
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Ethyl 3-[(1S)-1-(prop-2-ynylamino)ethyl]benzoate hydrochloride
Supplier: Apollo Scientific
Ethyl 3-[(1S)-1-(prop-2-ynylamino)ethyl]benzoate hydrochloride
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AMP (2-Amino-2-methylpropanol), (max. 5% H₂O) 95%
Supplier: Thermo Fisher Scientific
AMP (2-Amino-2-methylpropanol), (max. 5% H₂O) 95%
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EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride), No-Weigh™ Format, Pierce™
Supplier: Thermo Fisher Scientific
Thermo Scientific Pierce EDC is a carboxyl- and amine-reactive zero-length crosslinker. EDC reacts with a carboxyl group first and forms an amine-reactive O-acylisourea intermediate that quickly reacts with an amino group to form an amide bond with release of an isourea by-product. The intermediate is unstable in aqueous solutions and so two-step conjugation procedures rely on N-hydroxysuccinimide (NHS) for stabilization. Failure to react with an amine will result in hydrolysis of the intermediate, regeneration of the carboxyl, and release of an N-substituted urea. A side reaction is the formation of an N-acylurea, which is usually restricted to carboxyls located in hydrophobic regions of proteins.
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AMP (2-Amino-2-methylpropanol) 95%
Supplier: Apollo Scientific
Used for the preparation of buffer solutions, suitable for the determination of alkaline phosphatase.
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O-2-Propynylhydroxylamine hydrochloride 96%
Supplier: Apollo Scientific
O-2-Propynylhydroxylamine hydrochloride 96%
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Atomoxetine hydrochloride
Supplier: Thermo Fisher Scientific
Atomoxetine hydrochloride
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Dorsomorphin ≥98% (by TLC)
Supplier: ENZO LIFE SCIENCES
Cell-permeable pyrrazolopyrimidine derivative that inhibits AMP kinase (Ki=109nM in the absence of AMP) in an ATP-competitive manner. It displays no significant inhibition of ZAPK, SYK, PKCT, PKA and JAK3. Decreases food intake in mice and inhibits the effects of AICAR and metformin. It has been shown to inhibit BMP type I receptors ALK2, ALK3 and ALK6. Promotes cardiomyogenesis in mouse embryonic stem cells. Induces protective autophagy in cancer cell lines.
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4-Isopropyl-3-methylaniline hydrochloride 95%
Supplier: Apollo Scientific
4-Isopropyl-3-methylaniline hydrochloride 95%
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EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride) for synthesis
Supplier: Merck
EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride) for synthesis