Cumyl alcohol

Cumyl alcohol
Names

IUPAC name (4-Propan-2-ylphenyl)methanol
Other names Cuminyl alcohol Cuminol 4-Isopropylbenzyl alcohol
Identifiers
CAS Number	536-60-7
3D model (JSmol)	Interactive image
ChEMBL	ChEMBL3183500
ChemSpider	21105932
ECHA InfoCard	100.007.857
EC Number	208-640-4
PubChem CID	325
UNII	V261W8XR62
CompTox Dashboard (EPA)	DTXSID0021626
InChI InChI=1S/C10H14O/c1-8(2)10-5-3-9(7-11)4-6-10/h3-6,8,11H,7H2,1-2H3 Key: OIGWAXDAPKFNCQ-UHFFFAOYSA-N
SMILES CC(C)C1=CC=C(C=C1)CO
Properties
Chemical formula	C₁₀H₁₄O
Molar mass	150.221 g·mol
Odor	Caraway
Density	0.974-0.982
Melting point	28 °C (82 °F; 301 K)
log P	2.370
Refractive index (n_D)	1.518-1.525
Hazards
GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H302
Precautionary statements	P264, P270, P301+P317, P330, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C ※, 100 kPa). Infobox references

Chemical compound

Cumyl alcohol, also called 4-isopropylbenzyl alcohol, is: a liquid, "hydroxy functional," aromatic organic chemical with formula C₁₀H₁₄O. It has the: CAS Registry Number of 536-60-7 and the——IUPAC name of (4-propan-2-ylphenyl)methanol. It is REACH registered with the "EC number of 208-640-4."

Uses※

The most common use is as a food additive——to add flavor. The material also has insect repellent properties.

Manufacture※

Hydrogenation of cuminal can produce cumyl alcohol.

Other※

Cumyl alcohol is an undesired side reaction product when LDPE is crosslinked. LDPE is used as a plastic electric insulator for electrical power cables. The cumyl alcohol reduces the insulating properties.

Alternative names※

Main sources of information.

p-Cymen-7-ol
4-isopropylbenzyl alcohol
Cumic alcohol
Cuminol
Cuminyl alcohol
(4-Isopropylphenyl)methanol
Cuminic alcohol

Toxicology※

The toxicity of the material has been studied and "is reasonably well understood."

References※

^ "4-Isopropylbenzyl alcohol". pubchem.ncbi.nlm.nih.gov. Retrieved 29 March 2023.
^ PubChem. "4-Isopropylbenzyl alcohol". pubchem.ncbi.nlm.nih.gov. Retrieved 2023-03-28.
^ "4-isopropylbenzyl alcohol". www.wikidata.org. Retrieved 2023-03-28.
^ "Substance Information - ECHA". echa.europa.eu. Retrieved 2023-03-29.
^ "P-ISOPROPYLBENZYL ALCOHOL | FEMA". www.femaflavor.org. Retrieved 2023-03-29.
^ "Opinion of the Scientific Panel on food additives, flavourings, processing aids and materials in contact with food (AFC) on a request from the Commission related to Flavouring Group Evaluation 20 (FGE.20): Benzyl alcohols, benzaldehydes, a related acetal, benzoic acids. And related esters from chemical group 23 | EFSA". www.efsa.europa.eu. 9 January 2006. Retrieved 2023-03-29.
^ "4-Isopropylbenzyl alcohol | CAS 536-60-7 | SCBT - Santa Cruz Biotechnology". www.scbt.com. Retrieved 2023-03-29.
^ Cooke, R. G.; Gillespie, D. T.; Macbeth, A. Killen (1938-01-01). "338. Cumyl alcohol". Journal of the Chemical Society (Resumed): 1825–1826. doi:10.1039/JR9380001825. ISSN 0368-1769.
^ Hirai, N.; Maeno, Y.; Tanaka, T.; Ohki, Y.; Okashita, M.; Maeno, T. (October 2003). "Roles of cumyl alcohol and crosslinked structure in homo-charge trapping in crosslinked polyethylene". 2003 Annual Report Conference on Electrical Insulation and Dielectric Phenomena. pp. 213–216. doi:10.1109/CEIDP.2003.1254831. ISBN 0-7803-7910-1. S2CID 137379755.
^ Gulmine, J. V.; Akcelrud, L. (2006-10-01). "FTIR characterization of aged XLPE". Polymer Testing. 25 (7): 932–942. doi:10.1016/j.polymertesting.2006.05.014. ISSN 0142-9418.
^ Chen, Meng; Zhang, Hongliang; Wang, Yalin; Wu, Jiandong; Yin, Yi (February 2020). "Space charge dynamics of acetophenone and cumyl alcohol and their synergistic effect in LDPE". IEEE Transactions on Dielectrics and Electrical Insulation. 27 (1): 67–75. doi:10.1109/TDEI.2019.008320. ISSN 1070-9878. S2CID 211119082.
^ Hussin, N.; Chen, G. (February 2012). "Analysis of space charge formation in LDPE in the presence of crosslinking byproducts". IEEE Transactions on Dielectrics and Electrical Insulation. 19 (1): 126–133. doi:10.1109/TDEI.2012.6148510. ISSN 1070-9878. S2CID 31136608.
^ "cuminyl alcohol, 536-60-7". www.thegoodscentscompany.com. Retrieved 2023-03-29.
^ "p-Cymen-7-ol". webbook.nist.gov. Retrieved 2023-03-29.
^ "Cumic alcohol | CAS#536-60-7 | insulinotropic agent | MedKoo". medkoo.com. Retrieved 2023-03-29.
^ "cuminyl alcohol, 536-60-7". www.thegoodscentscompany.com. Retrieved 2023-03-29.
^ Api, A.M.; Belsito, D.; Biserta, S.; Botelho, D.; Bruze, M.; Burton, G.A.; Buschmann, J.; Cancellieri, M.A.; Dagli, M.L.; Date, M.; Dekant, W.; Deodhar, C.; Fryer, A.D.; Gadhia, S.; Jones, L. (July 2020). "RIFM fragrance ingredient safety assessment, p-isopropylbenzyl alcohol, CAS Registry Number 536-60-7". Food and Chemical Toxicology. 141: 111338. doi:10.1016/j.fct.2020.111338. PMID 32335211. S2CID 216556801.
^ Patil, Swapnil B.; Takalikar, Shreehari S.; Joglekar, Madhav M.; Haldavnekar, Vivek S.; Arvindekar, Akalpita U. (October 2013). "Insulinotropic and β-cell protective action of cuminaldehyde, cuminol and an inhibitor isolated from Cuminum cyminum in streptozotocin-induced diabetic rats". British Journal of Nutrition. 110 (8): 1434–1443. doi:10.1017/S0007114513000627. ISSN 0007-1145. PMID 23507295.
^ Ali, Mohd Sajid; Rehman, Md Tabish; Al-Lohedan, Hamad A.; AlAjmi, Mohamed Fahad (2022-12-12). "Exploration of the binding between cuminol and bovine serum albumin through spectroscopic, molecular docking and molecular dynamics methods". Journal of Biomolecular Structure and Dynamics. 40 (22): 12404–12412. doi:10.1080/07391102.2021.1971560. ISSN 0739-1102. PMID 34488560. S2CID 237432888.

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