1-Methylcyclohexanol

99%

Reagent Code: #204766
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Alias 1-Methylcyclohexanol
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CAS Number 590-67-0

science Other reagents with same CAS 590-67-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 114.19 g/mol
Formula C₇H₁₄O
badge Registry Numbers
EC Number 209-688-9
MDL Number MFCD00003857
thermostat Physical Properties
Melting Point 24-26 °C(lit.)
Boiling Point 168 °C752 mm Hg(lit.)
inventory_2 Storage & Handling
Density 0.919 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the production of fragrances and flavoring agents. It serves as a building block for creating more complex cyclic compounds due to its stable cyclohexane ring with a reactive hydroxyl group. Commonly employed in the synthesis of perfumes, where it contributes to woody and camphoraceous notes. Also utilized in research settings for studying reaction mechanisms involving tertiary alcohols, such as dehydration and oxidation reactions. Its methyl-substituted structure makes it valuable for steric effects in synthetic pathways.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿174.00
5g
10-20 days ฿180.00
25g
10-20 days ฿900.00
100g
10-20 days ฿3,220.00
500g
10-20 days ฿16,020.00
1-Methylcyclohexanol
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Used as an intermediate in organic synthesis, particularly in the production of fragrances and flavoring agents. It serves as a building block for creating more complex cyclic compounds due to its stable cyclohexane ring with a reactive hydroxyl group. Commonly employed in the synthesis of perfumes, where it contributes to woody and camphoraceous notes. Also utilized in research settings for studying reaction mechanisms involving tertiary alcohols, such as dehydration and oxidation reactions. Its methyl-

Used as an intermediate in organic synthesis, particularly in the production of fragrances and flavoring agents. It serves as a building block for creating more complex cyclic compounds due to its stable cyclohexane ring with a reactive hydroxyl group. Commonly employed in the synthesis of perfumes, where it contributes to woody and camphoraceous notes. Also utilized in research settings for studying reaction mechanisms involving tertiary alcohols, such as dehydration and oxidation reactions. Its methyl-substituted structure makes it valuable for steric effects in synthetic pathways.

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