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Reliable factory customized supply PHYTOL 150-86-7

  • Molecular Formula:C20H40O
  • Molecular Weight:296.537
  • Vapor Pressure:0mmHg at 25°C 
  • Melting Point:<25 °C 
  • Refractive Index:1.461-1.469  
  • Boiling Point:335.5 °C at 760 mmHg 
  • PKA:14.45±0.10(Predicted) 
  • Flash Point:157.5 °C 
  • PSA:20.23000 
  • Density:0.845 g/cm3 
  • LogP:6.36410 

PHYTOL(Cas 150-86-7) Usage

Safety Profile

Low toxicity by ingestion and skin contact. A skin irritant. When heated to decomposition it emits acrid smoke and irritating fumes.

Definition

ChEBI: A diterpenoid that is hexadec-2-en-1-ol substituted by methyl groups at positions 3, 7, 11 and 15.

Aroma threshold values

Low strength odor, floral type.

InChI:InChI=1/C20H40O/c1-17(2)9-6-10-18(3)11-7-12-19(4)13-8-14-20(5)15-16-21/h15,17-19,21H,6-14,16H2,1-5H3/b20-15+/t18-,19+/m0/s1

150-86-7 Relevant articles

Isolation, characterization and antioxidant, tyrosinase inhibitory activities of constituents from the flowers of cercis glabra ‘spring-1’

Shu, Penghua,Li, Yamin,Luo, Yuehui,Yu, Mengzhu,Fei, Yingying,Liu, Wanrong,Yang, Yuan,Wei, Xialan,Zhang, Yuhuan,Tu, Tieyao,Zhang, Lin

, p. 254 - 260 (2021/05/05)

A phytochemical study on the flowers of ...

New 29-nor-cycloartanes with a 3,4-seco- and a novel 2,3-seco-structure from the leaves of Sinocalycanthus chinensis

Kashiwada, Yoshiki,Nishimura, Kazuya,Kurimoto, Shin-Ichiro,Takaishi, Yoshihisa

experimental part, p. 2790 - 2796 (2011/06/19)

Eight new triterpenoids, including sinoc...

Stereocontrol of 1,5-related stereocentres using an intermediate silyl group-the diastereoselectivity of nucleophilic attack on a double bond adjacent to a stereogenic carrying a silyl group

Fleming, Ian,Maiti, Pranab,Ramarao, Chandrashekar

, p. 3989 - 4004 (2007/10/03)

R-5-Methylcyclohex-2-enone 1 reacts succ...

A convenient and asymmetric protocol for the synthesis of natural products containing chiral alkyl chains via Zr-catalyzed asymmetric carboalumination of alkenes. Synthesis of phytol and vitamins E and K.

Huo,Negishi

, p. 3253 - 3256 (2007/10/03)

[reaction: see text]. A convenient and a...

150-86-7 Process route

1-O-α-L-rhamnosyl-(E)-phytol

1-O-α-L-rhamnosyl-(E)-phytol

L-Rhamnose
3615-41-6,478518-52-4

L-Rhamnose

phytol
150-86-7,844467-91-0

phytol

Conditions
Conditions Yield
With hydrogenchloride; water; In methanol; for 3h; Reflux;
methanol
67-56-1

methanol

sinocalycanchinensin C
1310535-52-4

sinocalycanchinensin C

sinocalycanchinensin B
1310535-51-3

sinocalycanchinensin B

phytol
150-86-7,844467-91-0

phytol

Conditions
Conditions Yield
methanol; sinocalycanchinensin C; With sodium methylate; at 60 ℃; for 24h;
In methanol;
1.2 mg
2.4 mg

150-86-7 Upstream products

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    (2E,7R,11R)-3,7,11,15-tetramethyl-hexadec-2-enoic acid methyl ester

  • 101541-51-9
    101541-51-9

    (2Z,7R,11R)-3,7,11,15-tetramethyl-hexadec-2-enoic acid ethyl ester

  • 7437-61-8
    7437-61-8

    2-methyl-3,4-epoxy-1-butene

  • 130627-55-3
    130627-55-3

    (3R,7R)-3,7,11-Trimethyldodecylmagnesium-bromid

150-86-7 Downstream products

  • 74515-24-5
    74515-24-5

    2.3.5-trimethyl-6-((7R:11R)-trans-phytyl)-hydroquinone

  • 119-13-1
    119-13-1

    dl-δ-tocopherol

  • 493-35-6
    493-35-6

    (2RS,4'R,8'R)-5,7-Dimethyl-tocol

  • 362-45-8
    362-45-8

    2,3-dimethoxy-5-methyl-6-((7R,11R)-trans-phytyl)-[1,4]benzoquinone

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