| Identification | Back Directory | [Name]
1,3-DIHYDROXY-5-TRICOSYLBENZEN | [CAS]
70110-60-0 | [Synonyms]
Tricosylresorcinol (23:0)
5-Tricosylresorcinol
5-Tricosyl-1,3-benzenediol
5-Tricosylbenzene-1,3-diol
1,3-Benzenediol, 5-tricosyl-
1,3-DIHYDROXY-5-TRICOSYLBENZEN | [EINECS(EC#)]
200-258-5 | [Molecular Formula]
C29H52O2 | [MDL Number]
MFCD09743630 | [MOL File]
70110-60-0.mol | [Molecular Weight]
432.72 |
| Chemical Properties | Back Directory | [Melting point ]
100 °C(Solv: cyclohexane (110-82-7)) | [Boiling point ]
550.0±20.0 °C(Predicted) | [density ]
0.929±0.06 g/cm3(Predicted) | [storage temp. ]
2-8°C | [solubility ]
Ethanol: soluble | [form ]
A crystalline solid | [pka]
9.55±0.10(Predicted) |
| Hazard Information | Back Directory | [Description]
5-Tricosylresorcinol is an alkylresorcinol that has been found in wheat, rye, triticale, and barley. It reduces hydrogen peroxide-induced DNA damage in HT-29 cells when used at a concentration of 100 μM. | [Uses]
5-n-Tricosylresorcinolthe is the first cyst lipid. 5-n-Tricosylresorcinolthe has metahydroxyl group which allows it to self-associate forming a staggered-chain conformation in which the polar head groups have heaxagonal symmetry. 5-n-Tricosylresorcinolthe reduces hydrogen peroxide-induced DNA damage[1][2]. | [Definition]
ChEBI: 5-tricosylresorcinol is a 5-alkylresorcinol that is resorcinol which is substituted by a tricosyl group at position 5. It is found in wheat bran. It has a role as a plant metabolite and a bacterial metabolite. | [References]
[1] Reusch RN, et al. Novel lipid components of the Azotobacter vinelandii cyst membrane. Nature. 1983;302(5905):268-270. DOI:10.1038/302268a0
[2] Parikka K, et al. In vitro antioxidant activity and antigenotoxicity of 5-n-alkylresorcinols. J Agric Food Chem. 2006;54(5):1646-1650. DOI:10.1021/jf052486e |
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