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3-Decyn-1-ol

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3-Decyn-1-ol Basic information

Product Name:
3-Decyn-1-ol
Synonyms:
  • TIMTEC-BB SBB008896
  • 2-HYDROXYETHYL-N-HEXYLACETYLENE
  • 3-DECYN-1-OL
  • 3-Decyne-1-ol
  • 3-DECYN-1-OL, 98%3-DECYN-1-OL, 98%3-DECYN-1-OL, 98%
  • 2-Hydroxyethylhexylacetylene
  • Ai3-37272
  • Hexyl(2-hydroxyethyl)acetylene
CAS:
51721-39-2
MF:
C10H18O
MW:
154.25
Product Categories:
  • Building Blocks
  • Chemical Synthesis
  • Acetylenes
  • Acetylenic Alcohols & Their Derivatives
  • Alkynes
  • Organic Building Blocks
  • Organic Building Blocks
  • Terminal
Mol File:
51721-39-2.mol
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3-Decyn-1-ol Chemical Properties

Melting point:
1.9°C (estimate)
Boiling point:
130-131 °C/22 mmHg (lit.)
Density 
0.877 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.459(lit.)
Flash point:
224 °F
pka
14.41±0.10(Predicted)
form 
clear liquid
color 
Colorless to Light orange to Yellow
Specific Gravity
0.877
Water Solubility 
Sparingly soluble in water (0.21 g/L) (25°C).
BRN 
1750909
CAS DataBase Reference
51721-39-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
2905.29.9000

MSDS

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3-Decyn-1-ol Usage And Synthesis

Uses

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 and as a reagent in the synthesis of methyl 9-decynoate.

Uses

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.

Synthesis Reference(s)

Tetrahedron Letters, 25, p. 5423, 1984 DOI: 10.1016/S0040-4039(01)91301-2

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.

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