10-Undecen-1-ol

98%

Reagent Code: #245030
label
Alias Undecyl alcohol, 10-undecen-1-ol, undecenol
fingerprint
CAS Number 112-43-6

science Other reagents with same CAS 112-43-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 170.29 g/mol
Formula C₁₁H₂₂O
badge Registry Numbers
EC Number 203-971-0
MDL Number MFCD00004750
thermostat Physical Properties
Melting Point -3 °C
Boiling Point 132-133 °C15 mm Hg(lit.)
inventory_2 Storage & Handling
Density 0.85 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of fragrances and flavor compounds due to its ability to undergo various chemical transformations, such as oxidation and esterification. Commonly employed in the production of macrocyclic musk compounds, which are valued in perfumery for their long-lasting scent and stability. Also utilized in the development of specialty polymers and surface modifiers, where its terminal double bond and hydroxyl group allow for functionalization and integration into larger molecular structures. Its reactivity makes it suitable for use in organic synthesis, particularly in creating bioactive molecules and fine chemicals.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿1,020.00
inventory 500g
10-20 days ฿20,030.00
inventory 100g
10-20 days ฿4,020.00
inventory 5g
10-20 days ฿350.00

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10-Undecen-1-ol
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Used as an intermediate in the synthesis of fragrances and flavor compounds due to its ability to undergo various chemical transformations, such as oxidation and esterification. Commonly employed in the production of macrocyclic musk compounds, which are valued in perfumery for their long-lasting scent and stability. Also utilized in the development of specialty polymers and surface modifiers, where its terminal double bond and hydroxyl group allow for functionalization and integration into larger molecu

Used as an intermediate in the synthesis of fragrances and flavor compounds due to its ability to undergo various chemical transformations, such as oxidation and esterification. Commonly employed in the production of macrocyclic musk compounds, which are valued in perfumery for their long-lasting scent and stability. Also utilized in the development of specialty polymers and surface modifiers, where its terminal double bond and hydroxyl group allow for functionalization and integration into larger molecular structures. Its reactivity makes it suitable for use in organic synthesis, particularly in creating bioactive molecules and fine chemicals.

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