| Identification | Back Directory | [Name]
PRIMIN | [CAS]
15121-94-5 | [Synonyms]
PRIMIN
Isolan
PRIMIN(P)
IsolanPRIMIN
2-Methoxy-6-pentyl-p-benzoquinone
2-Methoxy-6-phentyl-p-benzochinone
2-Pentyl-6-methoxy-1,4-benzoquinone
2-METHOXY-6-N-PENTYL-P-BENZOQUINONE
2-METHOXY-6-PENTYL-1,4-BENZOQUINONE
2-METHOXY-6-N-PENTYL-1,4-BENZOQUINONE
2-Methoxy-6-pentyl-2,5-cyclohexadiene-1,4-dione
2,5-Cyclohexadiene-1,4-dione, 2-methoxy-6-pentyl- | [Molecular Formula]
C12H16O3 | [MDL Number]
MFCD00221604 | [MOL File]
15121-94-5.mol | [Molecular Weight]
208.25 |
| Chemical Properties | Back Directory | [Melting point ]
77-79℃ | [Boiling point ]
163 °C(Press: 3 Torr) | [density ]
1.06±0.1 g/cm3 (20 ºC 760 Torr) | [solubility ]
Acetonitrile: soluble; Ethanol: soluble; Ethyl Acetate: soluble; Methanol: soluble | [form ]
A solid | [Contact allergens]
Primin is the major allergen of Primula obconica
Hance (Primulaceae family). Allergic contact dermatitis
is mainly occupational, occurring in florists and
horticulturists. |
| Hazard Information | Back Directory | [Definition]
ChEBI: A member of the class of 1,4-benzoquinones having a methoxy substituent at the 2-position and a pentyl substituent at the 6-position. | [Description]
Primin is the allergen of Primula obconica. Occupational
contact dermatitis occurs mainly in florists and
horticulturists. | [Uses]
Primin can be prepared to use for SAR docking and antioxidant activity due to the activity of COX/5-LOX inhibitors with quinone and resorcinol core. It can also be used for its cytotoxic mechanisms toward human acute lymphoblastic leukemia, multiple myeloma and acute myeloid leukemia cells. |
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