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ChemicalBook > Product Catalogue >Chemical Reagents >Organic reagents >Fatty alcohols >10-UNDECYN-1-OL

10-UNDECYN-1-OL

10-UNDECYN-1-OL Structure
  • ₹3528.95 - ₹11200
  • Product name: 10-UNDECYN-1-OL
  • CAS: 2774-84-7
  • MF: C11H20O
  • MW: 168.28
  • EINECS:
  • MDL Number:MFCD00041675
  • Synonyms:TIMTEC-BB SBB009008;10-UNDECYN-1-OL;10-UNDECY-1-OL;Undecynol;10-UNDECYN-1-OL 96%;10-Undecyn-1-ol,96%;undec-10-yn-1-ol;11-Hydroxy-1-undecyne
2 prices
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Brand

  • Sigma-Aldrich(India)
  • TCI Chemicals (India)

Package

  • 1ML
  • 5G
  • ManufacturerSigma-Aldrich(India)
  • Product number94195
  • Product description10-Undecyn-1-ol ≥95.0% (GC)
  • Packaging1ML
  • Price₹3528.95
  • Updated2022-06-14
  • Buy
  • ManufacturerTCI Chemicals (India)
  • Product numberU0055
  • Product description10-Undecyn-1-ol min. 95.0 %
  • Packaging5G
  • Price₹11200
  • Updated2022-05-26
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Sigma-Aldrich(India) 94195 10-Undecyn-1-ol ≥95.0% (GC) 1ML ₹3528.95 2022-06-14 Buy
TCI Chemicals (India) U0055 10-Undecyn-1-ol min. 95.0 % 5G ₹11200 2022-05-26 Buy

Properties

Melting point :10.3°C (estimate)
Boiling point :111-112°C 4mm
Density :0.877 g/mL at 20 °C(lit.)
refractive index :n20/D 1.457
Flash point :110-111°C/4mm
storage temp. :Inert atmosphere,Room Temperature
pka :15.20±0.10(Predicted)
form :clear liquid
color :Colorless to Light yellow to Light orange
Water Solubility :Immiscible with water.
BRN :1702764
CAS DataBase Reference :2774-84-7(CAS DataBase Reference)
EPA Substance Registry System :10-Undecyn-1-ol (2774-84-7)

Safety Information

Symbol(GHS):
Signal word:
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
Precautionary statements:

Description

10-Undecyn-1-ol exhibits an antifungal activity. It is also used in the esterification of pentanoic and stearic acids in the presence of lipase. It is also employed as a reagent in the preparation of 11-bromo-undec-1-yne by reacting with carbon tetrabromide and triphenylphosphine. Further, it acts as an intermediate in synthetic chemistry. In addition to this, it serves as a precursor in organic synthesis.

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