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Ethyl 6-Hydroxyhexanoate

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Ethyl 6-Hydroxyhexanoate Basic information

Product Name:
Ethyl 6-Hydroxyhexanoate
Synonyms:
  • ETHYL 6-HYDROXYHEXANOATE
  • RARECHEM AK ML 0053
  • 6-Hydroxycaproic acid ethyl ester
  • 6-Hydroxyhexanoic acid ethyl ester
  • Ethyl 6-hydroxyhexanoate 97%
  • Hexanoic acid, 6-hydroxy-, ethyl ester
  • Ethyl 6-hydroxycaproate
CAS:
5299-60-5
MF:
C8H16O3
MW:
160.21
Product Categories:
  • C8 to C9
  • Carbonyl Compounds
  • Esters
Mol File:
5299-60-5.mol
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Ethyl 6-Hydroxyhexanoate Chemical Properties

Boiling point:
127-128 °C/12 mmHg (lit.)
Density 
0.985 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.437(lit.)
Flash point:
>230 °F
storage temp. 
Sealed in dry,Room Temperature
form 
clear liquid
pka
15.15±0.10(Predicted)
color 
Colorless to Almost colorless
InChI
InChI=1S/C8H16O3/c1-2-11-8(10)6-4-3-5-7-9/h9H,2-7H2,1H3
InChIKey
HYXRUZUPCFVWAH-UHFFFAOYSA-N
SMILES
C(OCC)(=O)CCCCCO
LogP
0.917 (est)
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Safety Information

WGK Germany 
3
HS Code 
2918.19.9000

MSDS

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Ethyl 6-Hydroxyhexanoate Usage And Synthesis

Uses

Ethyl 6-Hydroxyhexanoate is used as a reagent in the synthesis of cross-reactive carbohydrate determinants (CCDs) as tools for in vitro allergy diagnosis. Ethyl 6-Hydroxyhexanoate is also used in the preparation of N-5-Carboxypentyl-1-deoxymannojirimycin (C181150); a ligand used for the preparation of an affinity resin specific for Man9 mannosidase.

Uses

Ethyl 6-hydroxyhexanoate is suitable for use in the synthesis of series of model phenol carbonate ester prodrugs having fatty acid-like structures. It may be used in the preparation of alkyl triflates. It may be used in the synthesis of ethyl 6-(trifluoromethylsulfonyloxy)hexanoate.

Synthesis Reference(s)

The Journal of Organic Chemistry, 38, p. 2786, 1973 DOI: 10.1021/jo00956a011
Synthetic Communications, 11, p. 599, 1981 DOI: 10.1080/00397918108063631

General Description

Ethyl 6-hydroxyhexanoate is an ethyl ester. Its concentration in bordeaux red wines has been evaluated. Two-step preparation of ethyl 6-hydroxyhexanoate via hydrolysis of e-caprolactone has been reported.

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