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6-HEPTEN-1-OL

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6-HEPTEN-1-OL Basic information

Product Name:
6-HEPTEN-1-OL
Synonyms:
  • HEPTEN(6-)-1-OL
  • 6-HEPTEN-1-OL, 96+%
  • 6-HEPTEN-1-OL
  • hept-6-en-1-ol
  • 6-Hepten-1-ol>
  • 6-HEPTEN-1-OL ISO 9001:2015 REACH
CAS:
4117-10-6
MF:
C7H14O
MW:
114.19
Product Categories:
  • omega-Functional Alkanols, Carboxylic Acids, Amines & Halides
  • omega-Unsaturated Alkanols
Mol File:
4117-10-6.mol
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6-HEPTEN-1-OL Chemical Properties

Melting point:
26°C (estimate)
Boiling point:
113 °C / 69mmHg
Density 
0,85 g/cm3
refractive index 
1.4380 to 1.4420
pka
15.19±0.10(Predicted)
form 
clear liquid
color 
Colorless to Almost colorless
InChI
InChI=1S/C7H14O/c1-2-3-4-5-6-7-8/h2,8H,1,3-7H2
InChIKey
UFULDTPDHIRNGS-UHFFFAOYSA-N
SMILES
C(O)CCCCC=C
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Safety Information

Risk Statements 
10
Safety Statements 
16
RIDADR 
1987
HazardClass 
3
PackingGroup 
III
HS Code 
2905299090
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6-HEPTEN-1-OL Usage And Synthesis

Uses

6-Hepten-1-ol has a floral and green odor and is commonly used as a flavoring agent in the food and beverage industry. In addition, it can be used as an intermediate in the synthesis of various organic compounds, including fragrances, pharmaceuticals, and agrochemicals. Its unique chemical properties make it an important ingredient in a variety of industrial processes, notably in the production of perfumes, air fresheners and cleaning agents.

Industrial uses

6-Hepten-1-ol is used as a flavoring agent in the food and beverage industry. Its fruity and pear-like aroma makes it suitable for creating or enhancing the taste of various fruit-flavored products, such as beverages, confectionery, and ice cream.

Synthesis

4-Bromo-1-butanol (15.3g,0.1mol) was dissolved in 100ml of anhydrous tetrahydrofuran, anhydrous tetrahydrofuran solution of allylmagnesium chloride (0.25mol,250ml,1M) and lithium tetrachlorocopperate (10mmol,0.2mol/L,50ml) were added dropwise at 0??, the reaction was continued for 15 hours, and then the reaction was stopped by addition of saturated ammonium chloride. After the reaction was continued for 15 hours, the reaction was aborted by adding appropriate amount of saturated ammonium chloride solution, the tetrahydrofuran was evaporated, and ethyl acetate was added to extract three times, the organic layer was dried with anhydrous sodium sulfate and the solvent was evaporated to obtain the crude product, and the decompression distillation yielded 6-hepten-1-ol (4) 9.8 g, with the yield of 86%.

6-HEPTEN-1-OLSupplier

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