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Sigma-Aldrich

3-Pentyn-1-ol

97%

Synonym(s):

1-Hydroxy-3-pentyne

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About This Item

Linear Formula:
CH3C≡CCH2CH2OH
CAS Number:
Molecular Weight:
84.12
Beilstein:
1735967
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

form

liquid

refractive index

n20/D 1.456 (lit.)

bp

154-157 °C (lit.)

density

0.912 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

CC#CCCO

InChI

1S/C5H8O/c1-2-3-4-5-6/h6H,4-5H2,1H3

InChI key

IDYNOORNKYEHHO-UHFFFAOYSA-N

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General description

Inhibiting effect of 3-pentyn-1-ol on the corrosion of iron in 1M HCl has been investigated. Reaction of 3-pentyn-1-ol with Fe3(CO)12 in CH3OH/KOH solution yields closed trinuclear hydridic complex (μ-H)Fe3(CO)933-[H3CCC(CH2)(CH2)CO]).

Application

3-Pentyn-1-ol was used in the synthesis of 4,4-bis(1-methyl-1H-indol-3-yl)pentan-1-ol.

Pictograms

FlameExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

129.2 °F - closed cup

Flash Point(C)

54 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Synthesis of bis (indolyl) alkanes by a site-selective gold-catalyzed addition of indoles to butynol derivatives.
Barluenga J, et al.
Journal of Organometallic Chemistry, 694(4), 546-550 (2009)
Reactions of Fe3(CO)12 with 2-methyl-3-butyn-1-ol and 3-pentyn-1-ol under basic methanolic conditions.
Bertolotti F, et al.
Journal of Organometallic Chemistry, 693(16), 2673-2678 (2008)
Inhibitive properties, adsorption and surface study of butyn-1-ol and pentyn-1-ol alcohols as corrosion inhibitors for iron in HCl.
Babic-Samardzija K, et al.
Journal of Materials Chemistry, 15(19), 1908-1916 (2005)

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