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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

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.)

functional group

hydroxyl

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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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
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
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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