(S)-1,1,1-Trifluoro-2-butylamine hydrochloride

95%

Reagent Code: #237624
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CAS Number 101054-96-0

science Other reagents with same CAS 101054-96-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 163.57 g/mol
Formula C₄H₉ClF₃N
badge Registry Numbers
MDL Number MFCD22380042
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active ingredients requiring high enantiomeric purity. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in drug design for improved bioavailability and resistance to degradation. Commonly employed in the preparation of agrochemicals and bioactive molecules where stereochemistry plays a critical role in activity. The hydrochloride salt form improves handling, stability, and solubility in aqueous reaction media.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,360.00
inventory 250mg
10-20 days ฿12,490.00
inventory 1g
10-20 days ฿27,150.00

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(S)-1,1,1-Trifluoro-2-butylamine hydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active ingredients requiring high enantiomeric purity. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in drug design for improved bioavailability and resistance to degradation. Commonly employed in the preparation of agrochemicals and bioactive molecules where stereochemistry plays a critical role in activity. The hydrochloride salt form improves handling,

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active ingredients requiring high enantiomeric purity. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in drug design for improved bioavailability and resistance to degradation. Commonly employed in the preparation of agrochemicals and bioactive molecules where stereochemistry plays a critical role in activity. The hydrochloride salt form improves handling, stability, and solubility in aqueous reaction media.

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