Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1945 1
1946 1
1947 2
1948 3
1949 1
1950 1
1951 3
1952 5
1953 2
1954 6
1955 15
1956 9
1957 7
1958 8
1959 7
1960 5
1961 5
1962 3
1963 5
1964 4
1965 3
1966 2
1968 4
1969 2
1971 5
1972 20
1973 36
1974 29
1975 22
1976 21
1977 12
1978 10
1979 11
1980 15
1981 16
1982 12
1983 18
1984 14
1985 18
1986 16
1987 29
1988 20
1989 22
1990 22
1991 25
1992 18
1993 20
1994 25
1995 33
1996 24
1997 36
1998 27
1999 40
2000 62
2001 57
2002 73
2003 49
2004 73
2005 79
2006 86
2007 78
2008 75
2009 76
2010 83
2011 94
2012 87
2013 71
2014 87
2015 80
2016 85
2017 86
2018 97
2019 76
2020 83
2021 64
2022 96
2023 64
2024 46

Text availability

Article attribute

Article type

Publication date

Search Results

2,437 results

Results by year

Filters applied: . Clear all
Page 1
Pentanol isomer synthesis in engineered microorganisms.
Cann AF, Liao JC. Cann AF, et al. Appl Microbiol Biotechnol. 2010 Jan;85(4):893-9. doi: 10.1007/s00253-009-2262-7. Epub 2009 Oct 27. Appl Microbiol Biotechnol. 2010. PMID: 19859707 Free PMC article. Review.
Pentanol isomers such as 2-methyl-1-butanol and 3-methyl-1-butanol are a useful class of chemicals with a potential application as biofuels. ...Through metabolic engineering, microbial strains for the production of these isomers have been developed, as well as that for 1-
Pentanol isomers such as 2-methyl-1-butanol and 3-methyl-1-butanol are a useful class of chemicals with a potential application as bi
RIFM fragrance ingredient safety assessment, 3-methyl-1-pentanol, CAS Registry Number 589-35-5.
Api AM, Belsito D, Botelho D, Browne D, Bruze M, Burton GA Jr, Buschmann J, Dagli ML, Date M, Dekant W, Deodhar C, Fryer AD, Joshi K, La Cava S, Lapczynski A, Liebler DC, O'brien D, Parakhia R, Patel A, Penning TM, Ritacco G, Romine J, Salvito D, Schultz TW, Sipes IG, Thakkar Y, Tokura Y, Tsang S, Wahler J. Api AM, et al. Food Chem Toxicol. 2018 May;115 Suppl 1:S26-S34. doi: 10.1016/j.fct.2017.11.036. Epub 2017 Nov 22. Food Chem Toxicol. 2018. PMID: 29175189 Review. No abstract available.
Fragrance material review on 4-methyl-2-pentanol.
McGinty D, Scognamiglio J, Letizia CS, Api AM. McGinty D, et al. Food Chem Toxicol. 2010 Jul;48 Suppl 4:S55-9. doi: 10.1016/j.fct.2010.05.028. Food Chem Toxicol. 2010. PMID: 20659636 Review.
A toxicologic and dermatologic review of 4-methyl-2-pentanol when used as a fragrance ingredient is presented. 4-Methyl-2-pentanol is a member of the fragrance structural group branched chain saturated alcohols. ...
A toxicologic and dermatologic review of 4-methyl-2-pentanol when used as a fragrance ingredient is presented. 4-Methyl-2-pentanol
3-Pentanol glycosides from root nodules of the actinorhizal plant Alnus cremastogyne.
Xu Y, Xu Y, Huang Z, Luo Y, Gao R, Xue J, Lin C, Pawlowski K, Zhou Z, Wei X. Xu Y, et al. Phytochemistry. 2023 Mar;207:113582. doi: 10.1016/j.phytochem.2022.113582. Epub 2022 Dec 31. Phytochemistry. 2023. PMID: 36596436
In this study, we isolated and identified three undescribed 3-pentanol glycosides, i.e., 3-pentyl alpha-l-arabinofuranosyl-(1''6')-beta-d-glucopyranoside, 3-pentyl alpha-l-rhamnopyranosyl-(1''6')-beta-d-glucopyranoside, and 3-pentyl 6'-(3-hydroxy3-methylglutaryl)-beta-d-gl …
In this study, we isolated and identified three undescribed 3-pentanol glycosides, i.e., 3-pentyl alpha-l-arabinofuranosyl-(1''6')-be …
Fragrance material review on 3-methyl-1-pentanol.
McGinty D, Scognamiglio J, Letizia CS, Api AM. McGinty D, et al. Food Chem Toxicol. 2010 Jul;48 Suppl 4:S93-6. doi: 10.1016/j.fct.2010.05.038. Food Chem Toxicol. 2010. PMID: 20659646 Review.
A toxicologic and dermatologic review of 3-methyl-1-pentanol when used as a fragrance ingredient is presented. 3-Methyl-1-pentanol is a member of the fragrance structural group branched chain saturated alcohols. ...
A toxicologic and dermatologic review of 3-methyl-1-pentanol when used as a fragrance ingredient is presented. 3-Methyl-1-pentanol
Pentanol and Benzyl Alcohol Attack Bacterial Surface Structures Differently.
Yano T, Miyahara Y, Morii N, Okano T, Kubota H. Yano T, et al. Appl Environ Microbiol. 2015 Oct 30;82(1):402-8. doi: 10.1128/AEM.02515-15. Print 2016 Jan 1. Appl Environ Microbiol. 2015. PMID: 26519389 Free PMC article.
Among the alcohols, Raman spectroscopic analyses showed that pentanol (pentyl alcohol [PeA]) and benzyl alcohol (BzA) accelerated the cellular accumulation of BAC. ...
Among the alcohols, Raman spectroscopic analyses showed that pentanol (pentyl alcohol [PeA]) and benzyl alcohol (BzA) accelerated the …
RIFM fragrance ingredient safety assessment, 2,3,4-trimethyl-3-pentanol, CAS Registry Number 3054-92-0.
Api AM, Belsito D, Botelho D, Bruze M, Burton GA Jr, Cancellieri MA, Chon H, Dagli ML, Date M, Dekant W, Deodhar C, Fryer AD, Jones L, Joshi K, Kumar M, Lapczynski A, Lavelle M, Lee I, Liebler DC, Moustakas H, Na M, Penning TM, Ritacco G, Romine J, Sadekar N, Schultz TW, Selechnik D, Siddiqi F, Sipes IG, Sullivan G, Thakkar Y, Tokura Y. Api AM, et al. Food Chem Toxicol. 2022 Jun;164 Suppl 1:113103. doi: 10.1016/j.fct.2022.113103. Epub 2022 May 4. Food Chem Toxicol. 2022. PMID: 35525380 No abstract available.
One-step lignocellulose fractionation using acid/pentanol pretreatment for enhanced fermentable sugar and reactive lignin production with efficient pentanol retrievability.
Madadi M, Zahoor, Song G, Karimi K, Zhu D, Elsayed M, Sun F, Abomohra A. Madadi M, et al. Bioresour Technol. 2022 Sep;359:127503. doi: 10.1016/j.biortech.2022.127503. Epub 2022 Jun 18. Bioresour Technol. 2022. PMID: 35728765
To valorize whole lignocellulosic biomass, this study proposed a biphasic solvent system using dilute acid (DA)/pentanol pretreatment. Effects of the key factors, i.e., temperature and pentanol concentration, on aspen were evaluated. Under identified optimal pretrea …
To valorize whole lignocellulosic biomass, this study proposed a biphasic solvent system using dilute acid (DA)/pentanol pretreatment …
Biofuels combustion.
Westbrook CK. Westbrook CK. Annu Rev Phys Chem. 2013;64:201-19. doi: 10.1146/annurev-physchem-040412-110009. Epub 2013 Jan 4. Annu Rev Phys Chem. 2013. PMID: 23298249 Review.
Two main classes of biofuels are described, those consisting of small, primarily alcohol, fuels (particularly ethanol, n-butanol, and iso-pentanol) that are used primarily to replace or supplement gasoline and those derived from fatty acids and used primarily to replace or …
Two main classes of biofuels are described, those consisting of small, primarily alcohol, fuels (particularly ethanol, n-butanol, and iso- …
Fragrance material review on 1-phenyl-3-methyl-3-pentanol.
Scognamiglio J, Jones L, Letizia CS, Api AM. Scognamiglio J, et al. Food Chem Toxicol. 2012 Sep;50 Suppl 2:S168-72. doi: 10.1016/j.fct.2011.10.016. Epub 2011 Oct 19. Food Chem Toxicol. 2012. PMID: 22033089 Review.
A toxicologic and dermatologic review of 1-phenyl-3-methyl-3-pentanol when used as a fragrance ingredient is presented. 1-Phenyl-3-methyl-3-pentanol is a member of the fragrance structural group Aryl Alkyl Alcohols and is a tertiary alcohol. ...This review contains …
A toxicologic and dermatologic review of 1-phenyl-3-methyl-3-pentanol when used as a fragrance ingredient is presented. 1-Phenyl-3-me …
2,437 results