2014
DOI: 10.1039/c4ra04791e
|View full text |Cite
|
Sign up to set email alerts
|

Terpenes in honey: occurrence, origin and their role as chemical biomarkers

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

3
68
0

Year Published

2014
2014
2024
2024

Publication Types

Select...
7

Relationship

2
5

Authors

Journals

citations
Cited by 61 publications
(78 citation statements)
references
References 112 publications
3
68
0
Order By: Relevance
“…The analyses were performed using two types of fibres covered with different coatings: polydimethylsiloxane/divinylbenzene (PDMS/DVB) ( A ) and divinylbenzene/carboxen/polydimethylsiloxane (DVB/CAR/PDMS) ( B ). The main compounds of the fir honey headspace were benzene carbonyls: benzaldehyde (19.0 – 43.7%, A ; 13.8 – 35.6%, B ) and phenylacetaldehyde (1.4 – 6.9%, A ; 0.0 – 11.9%, B ) that can be generated in the hive conditions by Strecker degradation or by the enzymatic transformation from the amino acid phenylalanine . Other group of dominant compounds were monoterpenes, predominantly linalool derivatives, i.e ., cis ‐linalool oxide (2.6 – 17.0%, A ; 3.8 – 20.5%, B ) and trans ‐linalool oxide (1.5 – 10.3%, A ; 2.4 – 13%, B ), hotrienol (4.4 – 19.7%, A ; 5.9 – 14.9%, B ) and lilac aldehyde isomers (2.0 – 19.2%, A ; 0 – 2.6%, B ).…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…The analyses were performed using two types of fibres covered with different coatings: polydimethylsiloxane/divinylbenzene (PDMS/DVB) ( A ) and divinylbenzene/carboxen/polydimethylsiloxane (DVB/CAR/PDMS) ( B ). The main compounds of the fir honey headspace were benzene carbonyls: benzaldehyde (19.0 – 43.7%, A ; 13.8 – 35.6%, B ) and phenylacetaldehyde (1.4 – 6.9%, A ; 0.0 – 11.9%, B ) that can be generated in the hive conditions by Strecker degradation or by the enzymatic transformation from the amino acid phenylalanine . Other group of dominant compounds were monoterpenes, predominantly linalool derivatives, i.e ., cis ‐linalool oxide (2.6 – 17.0%, A ; 3.8 – 20.5%, B ) and trans ‐linalool oxide (1.5 – 10.3%, A ; 2.4 – 13%, B ), hotrienol (4.4 – 19.7%, A ; 5.9 – 14.9%, B ) and lilac aldehyde isomers (2.0 – 19.2%, A ; 0 – 2.6%, B ).…”
Section: Resultsmentioning
confidence: 99%
“…Other group of dominant compounds were monoterpenes, predominantly linalool derivatives, i.e ., cis ‐linalool oxide (2.6 – 17.0%, A ; 3.8 – 20.5%, B ) and trans ‐linalool oxide (1.5 – 10.3%, A ; 2.4 – 13%, B ), hotrienol (4.4 – 19.7%, A ; 5.9 – 14.9%, B ) and lilac aldehyde isomers (2.0 – 19.2%, A ; 0 – 2.6%, B ). These compounds may be formed from linalool ( Scheme ) by a series of both enzymatic hydroxylation and oxidative transformations that may occur during the honey ripening in the hive . Other monoterpenes such as α ‐terpineol (0.0 – 1.2%, A ; 0.0 – 8.8%, B ) and borneol (0.4 – 4.8%, A ; 0.0 – 5.9%, B ) were present only with smaller percentages.…”
Section: Resultsmentioning
confidence: 99%
“…The higher concentration of hotrienol can partially help to explain the lack of fresh and clean characters in the heat‐exposed honey samples. Hotrienol is a compound that is typically produced from the dehydration of 2,6‐dimethyloacta‐1,7‐diene‐3,6‐diol during post‐harvest handling of honey …”
Section: Resultsmentioning
confidence: 99%
“…The geographic areas of the lavender and sage honey were in the same province, which may lead the bees harvesting from both area and caused similarities in volatile composition. Hotrienol comes from the flower, during ripening of the honey in the hive and is thermally generated during pasteurization …”
Section: Resultsmentioning
confidence: 99%