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3-Methyl-1-butyne, 96%, Thermo Scientific Chemicals
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Catalog number H53439.06
also known as H53439-06
Price (EUR)/ Each
89,91
Online exclusive
99.90 Save 9,99 (10%)
-
Quantity:
5 g
Price (EUR)/ Each
89,91
Online exclusive
99.90 Save 9,99 (10%)
3-Methyl-1-butyne, 96%, Thermo Scientific Chemicals
Catalog numberH53439.06
Price (EUR)/ Each
89,91
Online exclusive
99.90 Save 9,99 (10%)
-
Chemical Identifiers
CAS598-23-2
IUPAC Name3-methylbut-1-yne
Molecular FormulaC5H8
InChI KeyUSCSRAJGJYMJFZ-UHFFFAOYSA-N
SMILESCC(C)C#C
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Specifications
Specification Sheet
Specification SheetAppearance (Color)Clear colorless to pale yellow
FormLiquid
Assay (GC)>95%
3-Methyl-1-butyne is a terminal alkyne that under goes hydrosilylation reaction using phenylsilane. 3-Methyl-1-butyne is used as an intermediate for pharmaceuticals, in cosmetics and in chemical research.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
3-Methyl-1-butyne is a terminal alkyne that under goes hydrosilylation reaction using phenylsilane. 3-Methyl-1-butyne is used as an intermediate for pharmaceuticals, in cosmetics and in chemical research.
Solubility
Miscible with alcohol. Immiscible with water.
Notes
Store in cool place. Light and heat sensitive. Incompatible with strong oxidizing agents, acids and bases.
3-Methyl-1-butyne is a terminal alkyne that under goes hydrosilylation reaction using phenylsilane. 3-Methyl-1-butyne is used as an intermediate for pharmaceuticals, in cosmetics and in chemical research.
Solubility
Miscible with alcohol. Immiscible with water.
Notes
Store in cool place. Light and heat sensitive. Incompatible with strong oxidizing agents, acids and bases.
RUO – Research Use Only
General References:
- Smolyakov, V. M.; Grebeshkov, V. V. Calculating the properties of C2H2-C9H16alkynes, based on the additivity of energy contributions. Russ. J. Phys. Chem. A 2015, 89 (5), 914-918.
- Bernal, M. J.; Martin, M.; Sola, E. Allenyl to Alkenylcarbyne Tautomerization at the Ru-Si Bond of Ru(κP,P,Si) Pincer Complexes. Organometallics 2015, 34 (4), 800-803.