macrocarpal J

Modify Date: 2025-08-25 14:59:19

macrocarpal J structure	Common Name	macrocarpal J
	CAS Number	179603-47-5	Molecular Weight	490.629
	Density	1.2±0.1 g/cm3	Boiling Point	569.5±50.0 °C at 760 mmHg
	Molecular Formula	C₂₈H₄₂O₇	Melting Point	N/A
	MSDS	N/A	Flash Point	312.2±26.6 °C

Use of macrocarpal J

Macrocarpal J, a phloroglucinol?sesquiterpene-coupled compound, can be isolated from the leaves of Eucalyptus globulus[1].

Name	2,4,6-trihydroxy-5-[(1S)-1-[(4S)-4-hydroxy-6-(2-hydroxypropan-2-yl)-4,8a-dimethyl-1,2,3,4a,5,6,7,8-octahydronaphthalen-1-yl]-3-methylbutyl]benzene-1,3-dicarbaldehyde
Synonym	More Synonyms

Description	Macrocarpal J, a phloroglucinol?sesquiterpene-coupled compound, can be isolated from the leaves of Eucalyptus globulus[1].
Related Catalog	Research Areas >> Others Signaling Pathways >> Others >> Others
References	[1]. Osawa K, et al. Macrocarpals H, I, and J from the Leaves of Eucalyptus globulus. J Nat Prod. 1996 Sep;59(9):823-7.

Density	1.2±0.1 g/cm3
Boiling Point	569.5±50.0 °C at 760 mmHg
Molecular Formula	C₂₈H₄₂O₇
Molecular Weight	490.629
Flash Point	312.2±26.6 °C
Exact Mass	490.293060
PSA	135.29000
LogP	7.49
Vapour Pressure	0.0±1.6 mmHg at 25°C
Index of Refraction	1.600

Hazard Codes	Xi

1,3-Benzenedicarboxaldehyde, 5-[(1S)-1-[(1S,4R,4aR,6R,8aS)-decahydro-4-hydroxy-6-(1-hydroxy-1-methylethyl)-4,8a-dimethyl-1-naphthalenyl]-3-methylbutyl]-2,4,6-trihydroxy-

2,4,6-Trihydroxy-5-{(1S)-1-[(1S,4R,4aR,6R,8aS)-4-hydroxy-6-(2-hydroxy-2-propanyl)-4,8a-dimethyldecahydro-1-naphthalenyl]-3-methylbutyl}isophthalaldehyde

Macrocarpal J