Isopropyl myristate

Formula: C₁₇H₃₄O₂
Molecular weight: 270.4507
IUPAC Standard InChI: InChI=1S/C17H34O2/c1-4-5-6-7-8-9-10-11-12-13-14-15-17(18)19-16(2)3/h16H,4-15H2,1-3H3
IUPAC Standard InChIKey: AXISYYRBXTVTFY-UHFFFAOYSA-N
CAS Registry Number: 110-27-0
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: Tetradecanoic acid, 1-methylethyl ester; Myristic acid, isopropyl ester; Bisomel; Crodamol I.P.M.; Crodamol IPM; Deltyl Extra; Emcol-IM; Isomyst; Isopropyl tetradecanoate; Kessco IPM; Kesscomir; Promyr; Sinnoester MIP; Stepan D-50; Wickenol 101; Emerest 2314; Estergel; Ja-fa IPM; Kessco isopropyl myristate; Plymoutm IPM; Starfol IPM; Tegester; Tetradecanoic acid, isopropyl; Tetradecanoic acid, isopropyl ester; Unimate IPM; 1-Tridecanecarboxylic acid, isopropyl ester; D 50; 1-Methylethyl tetradecanoate; IPM; Lexol IPM; Liponate IPM; Radia 7190; Tegosoft M; iso-Propyl N-tetradecanoate; Methylethyl tetradecanoate; Tetradecanoic acid methyethyl ester; NSC 406280; component of Sardo Bath Oil; 1405-98-7
Permanent link for this species. Use this link for bookmarking this species for future reference.
Information on this page:
Other data available:
Options:
- Switch to calorie-based units

Data at NIST subscription sites:

NIST / TRC Web Thermo Tables, professional edition (thermophysical and thermochemical data)

NIST subscription sites provide data under the NIST Standard Reference Data Program, but require an annual fee to access. The purpose of the fee is to recover costs associated with the development of data collections included in such sites. Your institution may already be a subscriber. Follow the links above to find out more about the data in these sites and their terms of usage.

Van Den Dool and Kratz RI, non-polar column, temperature ramp

Go To: Top, References, Notes

Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Column type	Capillary	Capillary	Capillary	Capillary	Capillary
Active phase	HP-5MS	DB-5	HP-5	HP-5	HP-5
Column length (m)	30.	30.	30.	30.	30.
Carrier gas	He	He	He		He
Substrate
Column diameter (mm)	0.25	0.32	0.25		0.25
Phase thickness (μm)	0.25	0.25	0.25		0.25
T_start (C)	60.	40.	60.	50.	50.
T_end (C)	250.	250.	260.	290.	310.
Heat rate (K/min)	2.	5.	3.	4.	4.
Initial hold (min)	8.	2.
Final hold (min)	30.	5.
I	1823.	1812.	1830.	1829.	1817.
Reference	Benkaci-Ali, Baaliouamer, et al., 2007	Wu, Zorn, et al., 2007	Javidnia, Miri, et al., 2006	Magalhães, Ruiz, et al., 2005	Singer, Flach, et al., 2004
Comment	MSDC-RI	MSDC-RI	MSDC-RI	MSDC-RI	MSDC-RI

Column type	Capillary	Capillary	Capillary	Capillary	Capillary
Active phase	Optima 5	HP-5MS	HP-5	HP-5MS	HP-5
Column length (m)	25.	60.	30.	30.	30.
Carrier gas	He	He	He	He	He
Substrate
Column diameter (mm)	0.25	0.25	0.25	0.25	0.25
Phase thickness (μm)	0.25	0.25	0.25	0.25	0.25
T_start (C)	60.	40.	60.	60.	50.
T_end (C)	280.	310.	280.	280.	280.
Heat rate (K/min)	3.	3.	4.	4.	4.
Initial hold (min)		1.	5.	5.	5.
Final hold (min)	20.	20.
I	1812.	1831.	1827.	1827.	1824.
Reference	Chosson, Vérité, et al., 2003	Lalel, Singh, et al., 2003	Skaltsa, Demetzos, et al., 2003	Skaltsa, Mavrommati, et al., 2001	Lazari, Skaltsa, et al., 2000
Comment	MSDC-RI	MSDC-RI	MSDC-RI	MSDC-RI	MSDC-RI

Column type	Capillary
Active phase	SE-52
Column length (m)	25.
Carrier gas	He
Substrate
Column diameter (mm)	0.32
Phase thickness (μm)	0.25
T_start (C)	50.
T_end (C)	280.
Heat rate (K/min)	25.
Initial hold (min)	0.
Final hold (min)	0.
I	1817.
Reference	Casoli, Musini, et al., 1996
Comment	MSDC-RI

References

Go To: Top, Van Den Dool and Kratz RI, non-polar column, temperature ramp, Notes

Benkaci-Ali, Baaliouamer, et al., 2007
Benkaci-Ali, F.; Baaliouamer, A.; Meklati, B.Y.; Chemat, F., Chemical composition of seed essential oils from Algerian Nigella sativa extracted by microwave and hydrodistillation, Flavour Fragr. J., 2007, 22, 2, 148-153, https://doi.org/10.1002/ffj.1773 . [all data]

Wu, Zorn, et al., 2007
Wu, S.; Zorn, H.; Krings, U.; Berger, R.G., Volatiles from submerged and surface-cultured beefsteak fungus, Fistulina hepatica, Flavour Fragr. J., 2007, 22, 1, 53-60, https://doi.org/10.1002/ffj.1758 . [all data]

Javidnia, Miri, et al., 2006
Javidnia, K.; Miri, R.; Banani, A., Volatile oil constituents of Haplophyllum tuberculatum (Forssk.) A. Juss. (Rutaceae) from Iran, J. Essent. Oil Res., 2006, 18, 4, 355-356, https://doi.org/10.1080/10412905.2006.9699111 . [all data]

Magalhães, Ruiz, et al., 2005
Magalhães, A.F.; Ruiz, A.L.T.G.; Flach, A.; Faria, A.D.; Magalhães, E.G.; Amaral, M.C.E., Floral scent of Eleocharis elegans (Kunth) Roem. Schult. (Cyperaceae), Biochem. Syst. Ecol., 2005, 33, 7, 675-679, https://doi.org/10.1016/j.bse.2004.12.004 . [all data]

Singer, Flach, et al., 2004
Singer, R.B.; Flach, A.; Koehler, S.; Marsaioli, A.J.; Amaral, M.C.E., Sexual Mimicry in Mormolyca ringens (Lindl.) Schltr. (Orchidaceae: Maxillariinae), Ann. Bot. Rome, 2004, 93, 6, 755-762, https://doi.org/10.1093/aob/mch091 . [all data]

Chosson, Vérité, et al., 2003
Chosson, E.; Vérité, P.; Blanckaert, A.; Seguin, E.; Litaudon, M.; Sévenet, T., Non polar compounds from the bark of Sarcomelicope follicularis, Biochem. Syst. Ecol., 2003, 31, 10, 1185-1188, https://doi.org/10.1016/S0305-1978(03)00065-6 . [all data]

Lalel, Singh, et al., 2003
Lalel, H.J.D.; Singh, Z.; Chye Tan, S., Glycosidically-bound aroma volatile compounds in the skin and pulp of 'Kensington Pride' mango fruit at different stages of maturity, Postharvest Biol. Technol., 2003, 29, 2, 205-218, https://doi.org/10.1016/S0925-5214(02)00250-8 . [all data]

Skaltsa, Demetzos, et al., 2003
Skaltsa, H.D.; Demetzos, C.; Lazari, D.; Sokovic, M., Essential oil analysis and antimicrobial activity of eight Stachys species from Greece, Phytochemistry, 2003, 64, 3, 743-752, https://doi.org/10.1016/S0031-9422(03)00386-8 . [all data]

Skaltsa, Mavrommati, et al., 2001
Skaltsa, H.D.; Mavrommati, A.; Constantinidis, T., A chemotaxonomic investigation of volatile constituents in Stachys subsect. Swainsonianeae (Labiatae), Phytochemistry, 2001, 57, 2, 235-244, https://doi.org/10.1016/S0031-9422(01)00003-6 . [all data]

Lazari, Skaltsa, et al., 2000
Lazari, D.M.; Skaltsa, H.D.; Constantinidis, T., Volatile constituents of Centaurea pelia DC., C. thessala Hausskn. subsp. drakiensis (Freyn Sint.) Georg. and C. zuccariniana DC. from Greece, Flavour Fragr. J., 2000, 15, 1, 7-11, https://doi.org/10.1002/(SICI)1099-1026(200001/02)15:1<7::AID-FFJ860>3.0.CO;2-3 . [all data]

Casoli, Musini, et al., 1996
Casoli, A.; Musini, P.C.; Palla, G., Gas chromatographic-mass spectrometric approach to the problem of characterizing binding media in paintings, J. Chromatogr. A, 1996, 731, 1-2, 237-246, https://doi.org/10.1016/0021-9673(95)01194-3 . [all data]

Notes

Go To: Top, Van Den Dool and Kratz RI, non-polar column, temperature ramp, References

Symbols used in this document:

T_end Final temperature

T_start Initial temperature
Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
The National Institute of Standards and Technology (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data contained therein have been selected on the basis of sound scientific judgment. However, NIST makes no warranties to that effect, and NIST shall not be liable for any damage that may result from errors or omissions in the Database.
Customer support for NIST Standard Reference Data products.