422754
3-Decyn-1-ol
97%
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About This Item
Linear Formula:
CH3(CH2)5C≡CCH2CH2OH
CAS Number:
Molecular Weight:
154.25
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Form:
liquid
Product Name
3-Decyn-1-ol, 97%
InChI
1S/C10H18O/c1-2-3-4-5-6-7-8-9-10-11/h11H,2-6,9-10H2,1H3
SMILES string
CCCCCCC#CCCO
InChI key
YGEQBZUDPQQIFI-UHFFFAOYSA-N
assay
97%
form
liquid
refractive index
n20/D 1.459 (lit.)
bp
130-131 °C/22 mmHg (lit.)
density
0.877 g/mL at 25 °C (lit.)
functional group
hydroxyl
Application
3-Decyn-1-ol may be used in the following studies:
- As a starting material in the synthesis of 3′-deoxyribolactones.
- As a starting material in the synthesis of (Z)-3-decen-1-ol by hydrogenation over P-2 nickel.
- As a reagent in the synthesis of methyl 9-decynoate.
General description
3-Decyn-1-ol is primary homo-propargylic alcohol derivative. It has been reported to be formed during the isomerization of 2-decyn-1-ol in the presence of sodium salt of 1,3-diaminopropane. Its toxicity has been evaluated on the green alga, Pseudokirchneriella subcapitata in terms of EC50 (median effective concentration) and NOEC (no observed effect level) values. It undergoes semi hydrogenation in the presence of Lindlar catalyst to form cis-3-decen-1-ol.
signalword
Warning
hcodes
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
224.6 °F - closed cup
flash_point_c
107 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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The rearrangement of isomeric linear decyn-1-ols by reaction with the sodium salt of 1, 3-diaminopropane.
Macaulay SR.
Canadian Journal of Chemistry, 58(23), 2567-2572 (1980)
Seiji Itoh et al.
Bioscience, biotechnology, and biochemistry, 66(7), 1591-1596 (2002-09-13)
Both the (17R)- and (17S)-isomers of volicitin, which is contained in the oral secretion of the beet armyworm and induces corn seedlings to emit a blend of volatile compounds to attract the natural enemy of the herbivore, were synthesized via
Synthesis of 3'-Deoxyribolactones using a Hydrolysis-Induced Lactonization Cascade Reaction of Epoxy Cyanohydrins.
Vugts DJ, et al.
European Journal of Organic Chemistry, 2008(8), 1336-1339 (2008)
Tonibelle N Gatbonton-Schwager et al.
Redox biology, 2, 755-763 (2014-07-11)
4-Hydroxy-2-(E)-nonenal (4-HNE) is one of the major lipid peroxidation product formed during oxidative stress. At high concentrations, 4-HNE is cytotoxic and exerts deleterious effects that are often associated with the pathology of oxidative stress-driven disease. Alternatively, at low concentrations it
Chung Yuan Chen et al.
Journal of environmental monitoring : JEM, 14(1), 181-186 (2011-11-23)
The present study evaluates the toxicity of 34 propargylic alcohols, including primary, primary homo-, secondary, and tertiary alcohols, based on their effects on phytoplankton. A closed-system algal toxicity test was applied because the closed-system technique presents more realistic concentration-response relationships
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