Skip to Content
Merck
CN

545430

3-Octyn-1-ol

97%

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Linear Formula:
CH3(CH2)3C≡CCH2CH2OH
CAS Number:
Molecular Weight:
126.20
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
238-986-1
MDL number:
Assay:
97%
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


Quality Level

assay

97%

refractive index

n20/D 1.4569 (lit.)

density

0.880 g/mL at 25 °C (lit.)

functional group

hydroxyl

SMILES string

CCCCC#CCCO

InChI

1S/C8H14O/c1-2-3-4-5-6-7-8-9/h9H,2-4,7-8H2,1H3

InChI key

LRZGRGVRZSDRTK-UHFFFAOYSA-N

General description

3-Octyn-1-ol is a homopropargylic alcohol that can be prepared from 3-butyn-1-ol and 1-bromobutane.

Application

3-Octyn-1-ol may be used in the preparation of:
  • (3Z)-octen-1-ol
  • 7-octyn-1-ol
  • 3-cis-octenoic acid



pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

新产品

This item has



Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library



Pd/CaCO3 in liquid poly (ethylene glycol)(PEG): an easy and efficient recycle system for partial reduction of alkynes to cis-olefins under a hydrogen atmosphere.
Chandrasekhar S, et al.
Tetrahedron Letters, 45(11), 2421-2423 (2004)
Selective cleavage of dimethylhydrazones to the carbonyl compounds using silica gel and its application in the synthesis of (Z)-9-tetradecenyl acetate.
Mitra RB and Reddy GB.
Synthesis, 1989(09), 694-698 (1989)
Peter Witzgall et al.
Journal of chemical ecology, 31(12), 2923-2932 (2005-12-21)
Analysis of extracts of sex pheromone glands of grapevine moth females Lobesia botrana showed three previously unidentified compounds, (E)-7-dodecenyl acetate and the (E,E)- and (Z,E)-isomers of 7,9,11-dodecatrienyl acetate. This is the first account of a triply unsaturated pheromone component in



Global Trade Item Number

SKUGTIN
545430-5G04061837582011