D-Limonene
- Formula: C10H16
- Molecular weight: 136.2340
- IUPAC Standard InChIKey: XMGQYMWWDOXHJM-SNVBAGLBSA-N
- CAS Registry Number: 5989-27-5
- 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. - Stereoisomers:
- Other names: Cyclohexene, 1-methyl-4-(1-methylethenyl)-, (R)-; p-Mentha-1,8-diene, (R)-(+)-; (+)-(R)-Limonene; (+)-(4R)-Limonene; (+)-p-Mentha-1,8-diene; (+)-Limonene; (R)-(+)-Limonene; Carvene; D-(+)-Limonene; Limonene, (D)-; Limonene, (+)-; (R)-1-methyl-4-(1-methylethenyl)cyclohexene; Dextro-limonene; (R)-4-Isopropenyl-1-methyl-1-cyclohexene; 4-Isopropenyl-1-methyl-1-cyclohexene-, (R)-; (R)-Limonene; (+)-Dipentene; (4R)-(+)-Limonene; (4R)-Limonene; (R)-(+)-p-Mentha-1,8-diene; (R)-p-Mentha-1,8-diene; Biogenic SE 374; Cyclohexene, 1-methyl-4-(1-methylethenyl)-, (4R)-; EC 7; Glidesafe; Glidsafe; Refchole
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Condensed phase thermochemistry data
Go To: Top, Phase change data, IR Spectrum, Mass spectrum (electron ionization), 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: Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔcH°liquid | -1474.00 ± 0.50 | kcal/mol | Ccb | Hawkins and Eriksen, 1954 | Reanalyzed by Cox and Pilcher, 1970, Original value = -1473.9 ± 0.27 kcal/mol; Corresponding ΔfHºliquid = -13.03 kcal/mol (simple calculation by NIST; no Washburn corrections) |
Phase change data
Go To: Top, Condensed phase thermochemistry data, IR Spectrum, Mass spectrum (electron ionization), References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled as indicated in comments:
BS - Robert L. Brown and Stephen E. Stein
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
AC - William E. Acree, Jr., James S. Chickos
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
Tboil | 450. ± 2. | K | AVG | N/A | Average of 18 values; Individual data points |
Quantity | Value | Units | Method | Reference | Comment |
Tfus | 198.65 | K | N/A | Gomes, Serrano, et al., 1988 | Uncertainty assigned by TRC = 0.15 K; TRC |
Quantity | Value | Units | Method | Reference | Comment |
ΔvapH° | 11.8 | kcal/mol | N/A | Clara, Marigliano, et al., 2009 | Based on data from 326. to 445. K.; AC |
ΔvapH° | 11.9 | kcal/mol | GC | Hoskovec, Grygarová, et al., 2005 | Based on data from 313. to 413. K.; AC |
ΔvapH° | 11.9 | kcal/mol | GC | van Roon, Parsons, et al., 2002 | AC |
ΔvapH° | 11.9 | kcal/mol | CGC | Chickos, Hosseini, et al., 1995 | Based on data from 373. to 423. K.; AC |
ΔvapH° | 11.7 ± 0.02 | kcal/mol | C | Atik, Saito, et al., 1987 | AC |
Enthalpy of vaporization
ΔvapH (kcal/mol) | Temperature (K) | Method | Reference | Comment |
---|---|---|---|---|
11.0 ± 0.05 | 350. | EB | Steele, Chirico, et al., 2002 | Based on data from 339. to 495. K.; AC |
10.4 ± 0.05 | 390. | EB | Steele, Chirico, et al., 2002 | Based on data from 339. to 495. K.; AC |
9.78 ± 0.07 | 430. | EB | Steele, Chirico, et al., 2002 | Based on data from 339. to 495. K.; AC |
9.1 ± 0.1 | 470. | EB | Steele, Chirico, et al., 2002 | Based on data from 339. to 495. K.; AC |
11.8 | 300. | N/A | Espinosa Diaz, Guetachew, et al., 1999 | Based on data from 250. to 434. K.; AC |
10.6 | 302. | A | Stephenson and Malanowski, 1987 | Based on data from 287. to 448. K.; AC |
11.4 | 303. | A | Stephenson and Malanowski, 1987 | Based on data from 288. to 323. K.; AC |
Enthalpy of fusion
ΔfusH (kcal/mol) | Temperature (K) | Reference | Comment |
---|---|---|---|
2.720 | 199.2 | Gallis, van den Berg, et al., 1996 | See also Gallis, van den Berg, et al., 1996.; AC |
IR Spectrum
Go To: Top, Condensed phase thermochemistry data, Phase change data, Mass spectrum (electron ionization), 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
Gas Phase Spectrum
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Notice: Concentration information is not available for this spectrum and, therefore, molar absorptivity values cannot be derived.
Additional Data
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Download spectrum in JCAMP-DX format.
Owner | NIST Standard Reference Data Program Collection (C) 2018 copyright by the U.S. Secretary of Commerce on behalf of the United States of America. All rights reserved. |
---|---|
Origin | NIST Mass Spectrometry Data Center |
State | gas |
Instrument | HP-GC/MS/IRD |
Mass spectrum (electron ionization)
Go To: Top, Condensed phase thermochemistry data, Phase change data, IR Spectrum, 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
Spectrum
Notice: This spectrum may be better viewed with a Javascript and HTML 5 enabled browser.
Additional Data
View image of digitized spectrum (can be printed in landscape orientation).
Due to licensing restrictions, this spectrum cannot be downloaded.
Owner | NIST Mass Spectrometry Data Center Collection (C) 2014 copyright by the U.S. Secretary of Commerce on behalf of the United States of America. All rights reserved. |
---|---|
Origin | Japan AIST/NIMC Database- Spectrum MS-NW-1514 |
NIST MS number | 229344 |
References
Go To: Top, Condensed phase thermochemistry data, Phase change data, IR Spectrum, Mass spectrum (electron ionization), Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Hawkins and Eriksen, 1954
Hawkins, J.E.; Eriksen, W.T.,
Physical and thermodynamic properties of terpenes. II. The heats of combustion of some terpene hydrocarbons,
J. Am. Chem. Soc., 1954, 76, 2669-26. [all data]
Cox and Pilcher, 1970
Cox, J.D.; Pilcher, G.,
Thermochemistry of Organic and Organometallic Compounds, Academic Press, New York, 1970, 1-636. [all data]
Gomes, Serrano, et al., 1988
Gomes, A.; Serrano, L.; Fareio, F.,
Solid-Liquid Equilibria in 1,8-Cineole/TErpenic Hydrocarbon Systems,
J. Chem. Eng. Data, 1988, 33, 194. [all data]
Clara, Marigliano, et al., 2009
Clara, Rene A.; Marigliano, Ana C. Gomez; Solimo, Horacio N.,
Density, Viscosity, and Refractive Index in the Range (283.15 to 353.15) K and Vapor Pressure of α-Pinene, d -Limonene, (±)-Linalool, and Citral Over the Pressure Range 1.0 kPa Atmospheric Pressure,
J. Chem. Eng. Data, 2009, 54, 3, 1087-1090, https://doi.org/10.1021/je8007414
. [all data]
Hoskovec, Grygarová, et al., 2005
Hoskovec, Michal; Grygarová, Dana; Cvacka, Josef; Streinz, Ludvík; Zima, Jirí; Verevkin, Sergey P.; Koutek, Bohumír,
Determining the vapour pressures of plant volatiles from gas chromatographic retention data,
Journal of Chromatography A, 2005, 1083, 1-2, 161-172, https://doi.org/10.1016/j.chroma.2005.06.006
. [all data]
van Roon, Parsons, et al., 2002
van Roon, André; Parsons, John R.; Govers, Harrie A.J.,
Gas chromatographic determination of vapour pressure and related thermodynamic properties of monoterpenes and biogenically related compounds,
Journal of Chromatography A, 2002, 955, 1, 105-115, https://doi.org/10.1016/S0021-9673(02)00200-5
. [all data]
Chickos, Hosseini, et al., 1995
Chickos, James S.; Hosseini, Sarah; Hesse, Donald G.,
Determination of vaporization enthalpies of simple organic molecules by correlations of changes in gas chromatographic net retention times,
Thermochimica Acta, 1995, 249, 41-62, https://doi.org/10.1016/0040-6031(95)90670-3
. [all data]
Atik, Saito, et al., 1987
Atik, Zadjia; Saito, Yoshihiro; Kusano, Kazuhito,
Thermodynamic properties of liquid enantiomers I. Enthalpies of vaporization of fenchones, α-methylbenzylamines, and limonenes at 298.15 K,
The Journal of Chemical Thermodynamics, 1987, 19, 1, 99-102, https://doi.org/10.1016/0021-9614(87)90167-4
. [all data]
Steele, Chirico, et al., 2002
Steele, W.V.; Chirico, R.D.; Cowell, A.B.; Knipmeyer, S.E.; Nguyen, A.,
Thermodynamic Properties and Ideal-Gas Enthalpies of Formation for Methyl Benzoate, Ethyl Benzoate, ( R )-(+)-Limonene, tert -Amyl Methyl Ether, trans -Crotonaldehyde, and Diethylene Glycol,
J. Chem. Eng. Data, 2002, 47, 4, 667-688, https://doi.org/10.1021/je0100847
. [all data]
Espinosa Diaz, Guetachew, et al., 1999
Espinosa Diaz, M.A.; Guetachew, T.; Landy, P.; Jose, J.; Voilley, A.,
Experimental and estimated saturated vapour pressures of aroma compounds,
Fluid Phase Equilibria, 1999, 157, 2, 257-270, https://doi.org/10.1016/S0378-3812(99)00016-3
. [all data]
Stephenson and Malanowski, 1987
Stephenson, Richard M.; Malanowski, Stanislaw,
Handbook of the Thermodynamics of Organic Compounds, 1987, https://doi.org/10.1007/978-94-009-3173-2
. [all data]
Gallis, van den Berg, et al., 1996
Gallis, H.E.; van den Berg, G.J.K.; Oonk, H.A.J.,
Thermodynamic Properties of Crystalline d -Limonene Determined by Adiabatic Calorimetry,
J. Chem. Eng. Data, 1996, 41, 6, 1303-1306, https://doi.org/10.1021/je960094l
. [all data]
Notes
Go To: Top, Condensed phase thermochemistry data, Phase change data, IR Spectrum, Mass spectrum (electron ionization), References
- Symbols used in this document:
Tboil Boiling point Tfus Fusion (melting) point ΔcH°liquid Enthalpy of combustion of liquid at standard conditions ΔfusH Enthalpy of fusion ΔvapH Enthalpy of vaporization ΔvapH° Enthalpy of vaporization at standard conditions - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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