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Aminoacetaldehyde diethyl acetal ≥97%

Supplier: ALADDIN SCIENTIFIC

Description: Aminoacetaldehyde diethyl acetal ≥97%

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2-Amino-4'-methoxyacetophenone hydrochloride ≥95%

Supplier: ALADDIN SCIENTIFIC

Description: 2-Amino-4′-methoxyacetophenone hydrochloride is an organic building block.

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Aluminium oxide ≥99.9% (metals basis)

Supplier: ALADDIN SCIENTIFIC

Description: Aluminium oxide ≥99.9% (metals basis)

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Aminoacetaldehyde dimethyl acetal ≥98%

Catalog Number: (ALA107137-25G)

Supplier: ALADDIN SCIENTIFIC

Description: Aminoacetaldehyde dimethyl acetal reacts with sulfone, followed by hydrolysis and reductive amination by adding desired piperazine derivative to yield piperazine derivatives of 2-furanyl[1,2,4]triazolo[1,5-a][1,3,5]triazine. Aminoacetaldehyde dimethyl acetal was used in a study to develop a fluorescent substrate for aldehyde dehydrogenase.It was used in preparation of chitosan-dendrimer hybrids having various functional groups such as carboxyl, ester and poly(ethylene glycol). It was used in an efficient 3-step synthesis of a bicyclic proline analog from L-ascorbic acid and in 3-component reaction catalyzed by MgClO4 leading to α-aminophosphonates.

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Human Angiotensin II

Catalog Number: (ALA107852-25MG)

Supplier: ALADDIN SCIENTIFIC

Description: Human Angiotensin II

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4-(4-Aminophenyl)benzonitrile ≥95%

Catalog Number: (ALA134661-1G)

Supplier: ALADDIN SCIENTIFIC

Description: 4-(4-Aminophenyl)benzonitrile ≥95%

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Azido PEG ≥95%

Catalog Number: (ALA163313-1G)

Supplier: ALADDIN SCIENTIFIC

Description: Azide/azido functionalized methoxyl polyethylene glycol (mPEG-N3) is a monofunctional PEG derivative that can be used to modify proteins, peptides and other materials. Azide group can react with alkyne in aqueous solution catalyzed by copper. It can also be reduced into amine group easily. PEGylation can increase solubility and stability and reduce immunogenicity of peptides and proteins. It can also suppress the non-specific binding of charged molecules to the modified surfaces.

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