(S)-1-Phenylethane-1-thiol

95%

Reagent Code: #232630
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CAS Number 33877-11-1

science Other reagents with same CAS 33877-11-1

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scatter_plot Molecular Information
Weight 138.23 g/mol
Formula C₈H₁₀S
badge Registry Numbers
MDL Number MFCD08689897
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used primarily in the fragrance industry, this compound contributes a unique, intense floral and slightly sulfurous note to perfume formulations. It is particularly valued in small concentrations to add depth, warmth, and complexity to floral scents such as rose, jasmine, and gardenia. Due to its chiral nature, the (S)-enantiomer provides a more refined and natural aroma profile compared to the racemic mixture. It can also serve as a specialty intermediate in the synthesis of chiral sulfur-containing molecules for research in organic chemistry and pharmaceutical development.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿11,530.00
inventory 100mg
10-20 days ฿19,590.00
inventory 250mg
10-20 days ฿33,290.00

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(S)-1-Phenylethane-1-thiol
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Used primarily in the fragrance industry, this compound contributes a unique, intense floral and slightly sulfurous note to perfume formulations. It is particularly valued in small concentrations to add depth, warmth, and complexity to floral scents such as rose, jasmine, and gardenia. Due to its chiral nature, the (S)-enantiomer provides a more refined and natural aroma profile compared to the racemic mixture. It can also serve as a specialty intermediate in the synthesis of chiral sulfur-containing mol

Used primarily in the fragrance industry, this compound contributes a unique, intense floral and slightly sulfurous note to perfume formulations. It is particularly valued in small concentrations to add depth, warmth, and complexity to floral scents such as rose, jasmine, and gardenia. Due to its chiral nature, the (S)-enantiomer provides a more refined and natural aroma profile compared to the racemic mixture. It can also serve as a specialty intermediate in the synthesis of chiral sulfur-containing molecules for research in organic chemistry and pharmaceutical development.

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