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CAS NO.34825-70-2 1-AMINO-5-HEXENE

Product Features

CAS NO.34825-70-2 1-AMINO-5-HEXENE

Product Name

1-AMINO-5-HEXENE

Synonyms

RARECHEMANKA1437;1-AMINO-5-HEXENE;Hex-5-en-1-amine;hex-5-en-1-amineHCl;1-AMINO-5-HEXENE,98%1-AMINO-5-HEXENE,98%1-AMINO-5-HEXENE,98%1-AMINO-5-HEXENE,98%;5-Hexen-1-amine(9CI,ACI);5-Hexen-1-ylamine;1-amino-5-hexylene

CAS NO.

34825-70-2

Purity

98% min

MF

C6H13N

MW

99.17

Storage

Preserve in a well-closed container and keep in cool, dry place, avoid light.

Package

In fluoride bottle/ Fluoride drums/iron drums/plastic drums/IBC Tank ,etc.

Shipment method

By Sea, Air, Courier door to door, etc.

Loading Port

China any port, Beijing, Shanghai, Hong Kong etc.

Application

1-Amino-5-hexene (CAS NO. 34825-70-2) is mainly used as a specialty organic synthesis intermediate for the preparation of functionalized polymers, pharmaceuticals, agrochemicals, and other nitrogen-containing compounds.

Contact

Contact person: Mr.Benson Han

Email: inquiry@dakenchem.com

Frequently Asked Questions:

Q1: What is the main use of 1-Amino-5-hexene (CAS NO. 34825-70-2)?
A: 1-Amino-5-hexene (CAS NO. 34825-70-2) is mainly used as an organic synthesis intermediate for producing functional polymers, pharmaceutical intermediates, and specialty chemicals due to its reactive amino and vinyl groups.
Q2: What makes 1-Amino-5-hexene (CAS NO. 34825-70-2) useful in chemical synthesis?
A: 1-Amino-5-hexene (CAS NO. 34825-70-2) contains both a primary amine group and a terminal alkene group, allowing chemists to perform diverse transformations and introduce multiple functionalities into target molecules.

Application Cases

Case 1: Polymer Functionalization
1-Amino-5-hexene (CAS NO. 34825-70-2) can be used as a functional monomer or modification reagent to introduce amino-functional groups into polymer chains, improving adhesion, chemical reactivity, and surface properties.
Case 2: Pharmaceutical Intermediate Synthesis
Researchers use 1-Amino-5-hexene (CAS NO. 34825-70-2) as a building block in organic synthesis routes to construct nitrogen-containing molecules with further structural modifications.

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