2(3H)-Furanone, 5-ethyldihydro-
- Formula: C6H10O2
- Molecular weight: 114.1424
- IUPAC Standard InChIKey: JBFHTYHTHYHCDJ-UHFFFAOYSA-N
- CAS Registry Number: 695-06-7
- Chemical structure:
This structure is also available as a 2d Mol file - Other names: γ-Caprolactone; 4-Hexanolide; γ-Ethyl-γ-butyrolactone; γ-Ethylbutyrolactone; γ-Hexalactone; γ-Hexanolactone; Hexanoic acid, 4-hydroxy-, γ-lactone; 4-Hydroxyhexanoic acid lactone; γ-Ethyl-n-butyrolactone; Hexanolide-1,4; Tonkalide; Toukalide; 4-Ethyl-4-butanolide; 5-Ethyltetrahydro-2-furanone; Hexanoic acid, 4-hydroxy-, lactone; Dihydro-5-ethyl-2(3H)-furanone; 4-Ethylbutanolide; 5-Ethyldihydrofuran-2(3H)-one; Hexan-4-olide; 6-Caprolactone; NSC 134769; NSC 24255; 5-Ethyldihydro-2(3H)-furanone; Furan-2-one (3 H) 5-ethyl(dihydro); 2(3H)-Furanone-5-ethyldihydro-5; hexa-4-olide; 4-ethylbutanolide (γ-hexalactone); 4,5-Dihydro-5-ethyl-2(3H)furanone
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Van Den Dool and Kratz RI, non-polar column, temperature ramp
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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 | Capillary |
---|---|---|---|---|---|
Active phase | BPX-5 | HP-5MS | DB-5 | SPB-5 | Ultra-2 |
Column length (m) | 25. | 30. | 30. | 30. | 25. |
Carrier gas | He | He | He | He | H2 |
Substrate | |||||
Column diameter (mm) | 0.25 | 0.25 | 0.32 | 0.25 | 0.25 |
Phase thickness (μm) | 0.25 | 0.25 | 1. | 0.25 | 0.33 |
Tstart (C) | 50. | 60. | 40. | 60. | 40. |
Tend (C) | 300. | 250. | 230. | 250. | 280. |
Heat rate (K/min) | 5. | 4. | 5. | 4. | 3. |
Initial hold (min) | 5. | 2. | 4. | 2. | 2. |
Final hold (min) | 20. | 10. | 20. | 10. | |
I | 1074. | 1056. | 1047. | 1063. | 1056. |
Reference | Dickschat J.S., Wagner-Dobler I., et al., 2005 | Pino, Mesa, et al., 2005 | Mahajan, Goddik, et al., 2004 | Píno, Marbot, et al., 2004 | Ceva-Antunes, Bizzo, et al., 2003 |
Comment | MSDC-RI | MSDC-RI | MSDC-RI | MSDC-RI | MSDC-RI |
Column type | Capillary | Capillary | Capillary |
---|---|---|---|
Active phase | DB-1 | DB-1 | DB-5 |
Column length (m) | 50. | 60. | 0.32 |
Carrier gas | He | H2 | |
Substrate | |||
Column diameter (mm) | 0.32 | 0.32 | 1. |
Phase thickness (μm) | 1.05 | ||
Tstart (C) | 40. | 50. | 30. |
Tend (C) | 260. | 250. | 180. |
Heat rate (K/min) | 2. | 4. | 1.5 |
Initial hold (min) | 0.1 | 5. | |
Final hold (min) | 40. | ||
I | 1019. | 1003. | 1068. |
Reference | Wu, Kuo, et al., 1991 | Flath, Light, et al., 1990 | Guichard and Souty, 1988 |
Comment | MSDC-RI | MSDC-RI | MSDC-RI |
References
Go To: Top, Van Den Dool and Kratz RI, non-polar column, temperature ramp, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Dickschat J.S., Wagner-Dobler I., et al., 2005
Dickschat J.S.; Wagner-Dobler I.; Schulz S.,
The chafer pheromone buibuilactone and ant pyrazines are also produced by marine bacteria,
J. Chem. Ecol., 2005, 31, 4, 925-947, https://doi.org/10.1007/s10886-005-3553-9
. [all data]
Pino, Mesa, et al., 2005
Pino, J.A.; Mesa, J.; Muñoz, Y.; Martí, M.P.; Marbot, R.,
Volatile components from mango (Mangifera indica L.) cultivars,
J. Agric. Food Chem., 2005, 53, 6, 2213-2223, https://doi.org/10.1021/jf0402633
. [all data]
Mahajan, Goddik, et al., 2004
Mahajan, S.S.; Goddik, L.; Qian, M.C.,
Aroma Compounds in Sweet Whey Powder,
J. Dairy Sci., 2004, 87, 12, 4057-4063, https://doi.org/10.3168/jds.S0022-0302(04)73547-X
. [all data]
Píno, Marbot, et al., 2004
Píno, J.A.; Marbot, R.; Vázquez, C.,
Volatile components of the fruits of Vangueria madagascariensis J. F. Gmel. from Cuba,
J. Essent. Oil Res., 2004, 16, 4, 302-304, https://doi.org/10.1080/10412905.2004.9698727
. [all data]
Ceva-Antunes, Bizzo, et al., 2003
Ceva-Antunes, P.M.N.; Bizzo, H.R.; Alves, S.M.; Antunes, O.A.C.,
Analysis of volatile compounds of taperebá (Spondias mombin L.) and Cajá (Spondias mombin L.) by simultaneous distillation and extraction (SDE) and solid phase microextraction (SPME),
J. Agric. Food Chem., 2003, 51, 5, 1387-1392, https://doi.org/10.1021/jf025873m
. [all data]
Wu, Kuo, et al., 1991
Wu, P.; Kuo, M.-C.; Hartman, T.G.; Rosen, R.T.; Ho, C.-T.,
Free and glycosidically bound aroma compounds in pineapple (Ananas comosus L. Merr.),
J. Agric. Food Chem., 1991, 39, 1, 170-172, https://doi.org/10.1021/jf00001a033
. [all data]
Flath, Light, et al., 1990
Flath, R.A.; Light, D.M.; Jang, E.B.; Mon, T.R.; John, J.O.,
Headspace Examination of Volatile Emissions from Ripening Papaya (Carica papaya L., Solo Variety),
J. Agric. Food Chem., 1990, 38, 4, 1060-1063, https://doi.org/10.1021/jf00094a032
. [all data]
Guichard and Souty, 1988
Guichard, E.; Souty, M.,
Comparison of the relative quantities of aroma compounds found in fresh apricot (Prunus armeniaca) from six different varieties,
Z. Lebensm. Unters. Forsch., 1988, 186, 4, 301-307, https://doi.org/10.1007/BF01027031
. [all data]
Notes
Go To: Top, Van Den Dool and Kratz RI, non-polar column, temperature ramp, References
- Symbols used in this document:
Tend Final temperature Tstart Initial temperature - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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