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2-Methyl-3-buten-2-ol / 1 L

Purity: 98 %
Synonym: Methylbutenol; 1,1-Dimethylallyl alcohol; 3-Hydroxy-3-methyl-1-butene
Molecular Formula: CH2'=CHC(CH3)2OH
Molecular Weight: 86.13
SKU: MND-51080
CAS Number: 115-18-4
MDL number: MFCD00004470
EC Number: 204-068-4
Form: liquid
Note: Prices are for comparison only. Contact Sales for current pricing.
Packing size: 1 L  
68.53 EUR



Safety Information


Hazard Statements

H225
H302
H315
H319

Precautionary Statements

P210
P305 + P351 + P338
P302 + P352
P301 + P312 + P330

Pictograms



Properties

Signal WordDanger
Flash Point (C)11 °C - closed cup
Flash Point (F)51.8 °F - closed cup
Vapor Pressure51 mmHg ( 25 °C)
Density0.824 g/mL at 25 °C (lit.)
Boiling Point98-99 °C (lit.)

 Product Description

2-Methyl-3-buten-2-ol is a chemical compound commonly used as a building block in the synthesis of flavors, fragrances, and pharmaceuticals. It is characterized by its unsaturated structure and alcohol functional group.

 

Application:

2-Methyl-3-buten-2-ol is utilized as a key intermediate in the production of flavoring agents, such as raspberry ketone, and fragrances, like lilac and jasmine. It also serves as a precursor in the synthesis of pharmaceutical compounds, contributing to various medicinal applications.

 

 

 

Articles:

- 2-methyl-3-buten-2-ol: A Pheromone Component of Conifer Bark Beetles Found in the Bark of Nonhost Deciduous Trees

Publication Date: 10 Apr 2012

Qing-He Zhang, Fredrik Schlyter and Göran Birgersson

https://doi.org/10.1155/2012/414508

 

- Comprehensive study of the thermodynamic properties for 2-methyl-3-buten-2-ol

Publication Date: Available online 29 July 2015

Dzmitry Zaitsau, Eugene Paulechka, Dzmitry S. Firaha, Andrey V. Blokhin, Gennady J. Kabo, Ala Bazyleva, Andrey G. Kabo, Mikhail A. Varfolomeev, Viktor M. Sevruk

https://doi.org/10.1016/j.jct.2015.07.028

 

- Hydroxyaldehyde Products from Hydroxyl Radical Reactions of Z-3-Hexen-1-ol and 2-Methyl-3-buten-2-ol Quantified by SPME and API-MS

Publication Date: September 10, 2003

Fabienne Reisen, Sara M. Aschmann, Roger Atkinson, and Janet Arey

https://doi.org/10.1021/es034142f