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      Hinokitiol

      • Product Name: Hinokitiol
      • CAS: 499-44-5
      • Purity:
      • Appearance:

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      Factory Supply industrial standard Hinokitiol 499-44-5 In Stock

      • Molecular Formula:C10H12O2
      • Molecular Weight:164.204
      • Vapor Pressure:8.98E-05mmHg at 25°C 
      • Melting Point:50-52 °C 
      • Refractive Index:1.553 
      • Boiling Point:303.4 °C at 760 mmHg 
      • PKA:7.06±0.30(Predicted) 
      • Flash Point:128.1 °C 
      • PSA:37.30000 
      • Density:1.127 g/cm3 
      • LogP:1.87580 

      Hinokitiol(Cas 499-44-5) Usage

      benefits

      Hinokitiol (β-thujaplicin) is a naturally occurring antioxidant, found in the heartwood of certain plants. It acts as a metal chelator and, also, enhances the activity of superoxide dismutase (Huang et al., 2015). It was found to be very protective in the assay. It has not been previously studied as a HC protectant. In addition to its antioxidant properties, hinokitiol has been shown to reduce inflammation via suppression of NFκB, and metalloproteinases, and to activate caspase 3. The former activities could contribute to its protective effect.Hinokitiol is a superpower ingredient that has anti-inflammatory, antioxidant, antibacterial, anti-fungal and anti-melanogenic properties. Best of all, hinokitiol is as gentle as it is powerful. Hinokitiol’s properties allow it to target the inflammatory redness and blemishes seen in rosacea and acne. Hinokitiol is effective against P. acnes bacteria, and there is no known acquired resistance to it, unlike other prescription antibiotics.

      Safety

      The safety of hinokitiol has been tested in rats and no carcinogenic effect to rats was found.In 2006, hinokitiol was categorized under the Domestic substances list (DSL) in Canada as non-persistent, non-bioaccumulative and non-toxic to aquatic organisms.

      Anticancer Research

      Studied in xenograft tumors such lung adenocarcinoma cell, EGFR-TKI-resistantlines PC9-IR and H1975 in which the growth inhibition was observed, a novel antitumormechanism was hypothesized. In summary, the hinokitiol can induce DNAdamage and autophagy (Rodrigues et al. 2015).

      Definition

      ChEBI: A monoterpenoid that is cyclohepta-2,4,6-trien-1-one substituted by a hydroxy group at position 2 and an isopropyl group at position 4. Isolated from Thuja plicata and Chamaecyparis obtusa, it exhibits antimicrobial activities.

      InChI:InChI=1/C10H12O2/c1-7(2)8-4-3-5-9(11)10(12)6-8/h3-7H,1-2H3,(H,11,12)

      499-44-5 Relevant articles

      Method for preparing hinokitiol

      -

      Paragraph 0083-0086, (2019/01/23)

      The invention discloses a method for pre...

      Method for preparing high-purity hinokitiol and coordination complex thereof

      -

      Paragraph 0060; 0061, (2018/10/19)

      The invention belongs to the technical f...

      A high-purity chinese juniper methyl alcohol of preparation method (by machine translation)

      -

      , (2018/08/03)

      The invention discloses a method for pre...

      Preparation method of beta-thujaplicine

      -

      Paragraph 0028; 0029; 0030; 0031; 0032; 0035; 0036, (2018/11/03)

      The invention belongs to the technical f...

      499-44-5 Process route

      4-bromo-2-hydroxycycklohepta-2,4,6-trien-1-one
      698-47-5

      4-bromo-2-hydroxycycklohepta-2,4,6-trien-1-one

      isopropenyltrimethylstannane
      3043-46-7

      isopropenyltrimethylstannane

      hinokitiol
      499-44-5

      hinokitiol

      Conditions
      Conditions Yield
      4-bromo-2-hydroxycycklohepta-2,4,6-trien-1-one; isopropenyltrimethylstannane; With bis-triphenylphosphine-palladium(II) chloride; In 1,4-dioxane; for 1h; Reflux;
      With 5%-palladium/activated carbon; hydrogen; In ethanol; at 20 ℃; for 24h; under 760.051 Torr;
      53%
      isopropoxyboronic acid
      52732-22-6

      isopropoxyboronic acid

      2-hydroxy-4-chloro-2,4,6-cycloheptatrien-1-one
      698-48-6

      2-hydroxy-4-chloro-2,4,6-cycloheptatrien-1-one

      hinokitiol
      499-44-5

      hinokitiol

      Conditions
      Conditions Yield
      With potassium phosphate; In tetrahydrofuran; at 100 ℃; for 2h;
      97.5%

      499-44-5 Upstream products

      • 35193-01-2
        35193-01-2

        β-isopropyltropolone

      • 55076-44-3
        55076-44-3

        1-isopropyl-8-oxa-bicyclo[3.2.1]oct-6-en-3-one

      • 10599-59-4
        10599-59-4

        2-isopropylfuran

      • 55076-46-5
        55076-46-5

        3-Isopropylcyclohepta-2,6-dienon

      499-44-5 Downstream products

      • 55076-49-8
        55076-49-8

        2-amino-6-isopropyl-cycloheptatrienone

      • 103028-78-0
        103028-78-0

        2-amino-4-isopropyl-cycloheptatrienone

      • 108973-66-6
        108973-66-6

        2-benzylamino-6-isopropyl-cycloheptatrienone

      • 108975-97-9
        108975-97-9

        2-benzylamino-4-isopropyl-cycloheptatrienone

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