2-Butene-1,4-diol(cistrans)

98%

Reagent Code: #143108
label
Alias 1,4-butene glycol (trans + cis); 1,4-dihydroxy-2-butene
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CAS Number 110-64-5

science Other reagents with same CAS 110-64-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 88.11 g/mol
Formula C₄H₈O₂
badge Registry Numbers
EC Number 203-787-0
MDL Number MFCD00063207
thermostat Physical Properties
Melting Point 4-10 °C(lit.)
Boiling Point 235 °C(lit.)
inventory_2 Storage & Handling
Density 1.072 g/mL at 20 °C(lit.)
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals, agrochemicals, and fine chemicals. It serves as a building block for the preparation of polymers and resins due to its bifunctional alcohol groups. Also employed in the synthesis of vitamins, fragrances, and specialty surfactants. Its reactivity allows for easy modification through hydrogenation, oxidation, or coupling reactions, making it valuable in multi-step synthetic routes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿230.00
inventory 100g
10-20 days ฿320.00
inventory 500g
10-20 days ฿1,190.00
inventory 2.5kg
10-20 days ฿5,340.00

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2-Butene-1,4-diol(cistrans)
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Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals, agrochemicals, and fine chemicals. It serves as a building block for the preparation of polymers and resins due to its bifunctional alcohol groups. Also employed in the synthesis of vitamins, fragrances, and specialty surfactants. Its reactivity allows for easy modification through hydrogenation, oxidation, or coupling reactions, making it valuable in multi-step synthetic routes.

Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals, agrochemicals, and fine chemicals. It serves as a building block for the preparation of polymers and resins due to its bifunctional alcohol groups. Also employed in the synthesis of vitamins, fragrances, and specialty surfactants. Its reactivity allows for easy modification through hydrogenation, oxidation, or coupling reactions, making it valuable in multi-step synthetic routes.

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