Citronellyl butyrate
- Formula: C14H26O2
- Molecular weight: 226.3550
- IUPAC Standard InChI: InChI=1S/C14H26O2/c1-5-7-14(15)16-11-10-13(4)9-6-8-12(2)3/h8,13H,5-7,9-11H2,1-4H3
- IUPAC Standard InChIKey: XQPZQXTWYZAXAK-UHFFFAOYSA-N
- CAS Registry Number: 141-16-2
- Chemical structure:
This structure is also available as a 2d Mol file or as a computed 3d SD file
The 3d structure may be viewed using Java or Javascript. - Other names: Butanoic acid, 3,7-dimethyl-6-octenyl ester; Butyric acid, 3,7-dimethyl-6-octenyl ester; Citronellyl n-butyrate; Natural rhodinol, butylated; Rhodinyl butyrate; 2,6-Dimethyl-2-octen-8-ol, butyrate; 2,6-Dimethyl-2-octen-8-yl butyrate; 6-Octen-1-ol, 3,7-dimethyl-, butyrate; 3,7-Dimethyl-6-octenyl butyrate; Citronellyl butanoate; 3,7-Dimethyl-6-octenyl butanoate; Butanoic acid, 3,7-dimethyl-6-octen-1-yl ester; Butyric acid, ester with citronellol; NSC 46147; 3,7-dimethyloct-6-en-1-yl butyrate; 134982-45-9; 76444-24-1
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- Other data available:
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Normal alkane RI, non-polar column, custom temperature program
Go To: Top, References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director
| Column type | Capillary | Capillary | Capillary | Capillary |
|---|---|---|---|---|
| Active phase | DB-1 | CP Sil 8 CB | CP Sil 8 CB | SE-30 |
| Column length (m) | 60. | 50. | 50. | |
| Carrier gas | Helium | He | He | |
| Substrate | ||||
| Column diameter (mm) | 0.25 | 0.32 | 0.32 | |
| Phase thickness (μm) | 0.25 | 0.25 | 0.25 | |
| Program | 50 0C (5 min) 3 0C/min -> 120 0C 5 0C/min -> 250 0C (3 min) 15 0C/min -> 300 0C (20 min) | 50C(5min) => 2C/min => 90C => 15C/min => 240C(4min) | 50C(5min) => 2C/min => 90C => 15C/min => 240C(4min) | not specified |
| I | 1513. | 1532. | 1532. | 1511. |
| Reference | Delort and Jaquier, 2009 | Butkienë, Nivinskienë, et al., 2005 | Butkienë, Nivinskienë, et al., 2004 | Vinogradov, 2004 |
| Comment | MSDC-RI | MSDC-RI | MSDC-RI | MSDC-RI |
References
Go To: Top, Normal alkane RI, non-polar column, custom temperature program, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Delort and Jaquier, 2009
Delort, E.; Jaquier, A.,
Novel terpenyl esters from Australian finger lime (Citrus australasica) peel extract,
Flav. Fragr. J., 2009, 24, 3, 123-132, https://doi.org/10.1002/ffj.1922
. [all data]
Butkienë, Nivinskienë, et al., 2005
Butkienë, R.; Nivinskienë, O.; Mockutë, D.,
α-Pinene chemotype of leaf (needle) essential oils of Juniperus communis L. growing wild in Vilnius district,
Chemija, 2005, 16, 1, 53-60. [all data]
Butkienë, Nivinskienë, et al., 2004
Butkienë, R.; Nivinskienë, O.; Mockutë, D.,
Chemical composition of unripe and ripe berry essential oils of Juniperus communis L. growing wild in Vilnius district,
Chemija, 2004, 15, 4, 57-63. [all data]
Vinogradov, 2004
Vinogradov, B.A.,
Production, composition, properties and application of essential oils, 2004, retrieved from http://viness.narod.ru. [all data]
Notes
Go To: Top, Normal alkane RI, non-polar column, custom temperature program, References
- Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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