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244430

Sigma-Aldrich

3-Hexyn-1-ol

98%

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About This Item

Linear Formula:
C2H5C≡CCH2CH2OH
CAS Number:
1002-28-4
Molecular Weight:
98.14
EC Number:
213-685-8
MDL number:
MFCD00002957
UNSPSC Code:
12352100
PubChem Substance ID:
24854676
NACRES:
NA.22

Quality Level

100

Assay

98%

form

liquid

refractive index

n20/D 1.454 (lit.)

bp

63-64 °C/12 mmHg (lit.)

density

0.898 g/mL at 25 °C (lit.)

SMILES string

CCC#CCCO

InChI

1S/C6H10O/c1-2-3-4-5-6-7/h7H,2,5-6H2,1H3

InChI key

ODEHKVYXWLXRRR-UHFFFAOYSA-N

Related Categories

General description

The stereoselective hydrogenation of 3-hexyn-1-ol was studied. Poly(N-vinyl-2-pyrrolidone)-stabilized Pd-nanoclusters showed an extraordinary catalytic performance in the selective hydrogenation of 3-hexyn-1-ol.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

145.4 °F - closed cup

Flash Point(C)

63 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKBZ9176V
MKBT0893V
MKBK3548V
MKBJ4788V
MKBH4688V

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Alexander Sachse et al.
Dalton transactions (Cambridge, England : 2003), 42(5), 1378-1384 (2012-10-12)
Well-dispersed Pd nanoparticles have been synthesized inside the mesoporosity of a silica monolith featuring hierarchical porosity of homogeneous interconnected macropores (4 microns) and mesopores (11 nm). These monoliths have been implemented as microreactors for selective hydrogenation reactions. Conversion and selectivity
Jules C A A Roelofs et al.
Chemical communications (Cambridge, England), (8)(8), 970-971 (2004-04-08)
Poly(N-vinyl-2-pyrrolidone)-stabilized Pd-nanoclusters, for the first time exclusively supported on the hydrotalcite lateral surface, showed a remarkable catalytic performance in the selective hydrogenation of 3-hexyn-1-ol, which can be ascribed to both the influence of the protecting polymer PVP as well as
Shigeru Tamogami et al.
FEBS letters, 589(3), 390-395 (2015-01-13)
The medicinal herbal plant Achyranthes bidentata (A. bidentata) produces the sweet-odor ester - methyl (E)-2-hexenoate (1) as the major volatile in response to methyl jasmonate (MeJA). Here, we investigated the biosynthetic pathway of methyl (E)-2-hexenoate (1). The common plant precursor

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