Phytosphingosine

Basic information

  • Product Name:Phytosphingosine
  • CasNo.:554-62-1
  • MF:C18H39NO3
  • MW:317.513

Physical and Chemical Properties

  • Purity:99%
  • Boiling Point:102 °C
  • Packing:
  • Throughput:
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Product Details

CasNo: 554-62-1

MF: C18H39NO3

Reputable factory supply Phytosphingosine 554-62-1 in stock with high standard

  • Molecular Formula:C18H39NO3
  • Molecular Weight:317.513
  • Vapor Pressure:2.18E-11mmHg at 25°C 
  • Melting Point:102 °C 
  • Refractive Index:9 ° (C=1, Pyridine) 
  • Boiling Point:483.733 °C at 760 mmHg 
  • PKA:11.91±0.45(Predicted) 
  • Flash Point:246.353 °C 
  • PSA:86.71000 
  • Density:0.983 g/cm3 
  • LogP:3.81930 

PHYTOSPHINGOSINE(Cas 554-62-1) Usage

Flammability and Explosibility

Notclassified

Veterinary Drugs and Treatments

Phytosphingosine is a unique topical antiseborrheic compound. It is in a class called ceramides which are waxy materials meant to meant to mimic the normal lipid composition of the stratum corneum. It may also have some antiinflammatory and antimicrobial properties.

InChI:InChI=1/C18H39NO3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-17(21)18(22)16(19)15-20/h16-18,20-22H,2-15,19H2,1H3/t16-,17+,18-/m0/s1

554-62-1 Relevant articles

-

Prostenik,M. et al.

, p. 651 - 655 (1965)

-

Isolation and structure of a new ceramide from the basidiomycete Hygrophorus eburnesus

Qu, Yan,Zhang, Hong-Bin,Liu, Ji-Kai

, p. 241 - 244 (2004)

A new ceramide, named hygrophamide (1), ...

Phytoceramides and acylated phytosterol glucosides from Pterospermum acerifolium Willd. seed coat and their osteogenic activity

Dixit, Preety,Chand, Kailash,Khan, Mohd Parvez,Siddiqui, Jawed Akhtar,Tewari, Deepshikha,Ngueguim, Florence Tsofack,Chattopadhyay, Naibedya,Maurya, Rakesh

, p. 117 - 125 (2012)

Phytochemical investigation of seed coat...

Paxillamide: A novel phytosphingosine derivative from the fruiting bodies of Paxillus panuoides

Gao, Jin-Ming,Zhang, An-Ling,Zhang, Cun-Li,Liu, Ji-Kai

, p. 1483 - 1487 (2004)

The new phytosphingosine-type ceramide 1...

Convergent evolution of bacterial ceramide synthesis

Ashley, Ben,Campopiano, Dominic J.,Chamberlain, Joshua D.,Coleman, Aimiyah,D’Emilia, Rachel,Fu, Larina,Guan, Ziqiang,Hansen, Matthew E. B.,Klein, Eric A.,Mohan, Eric C.,Nguyen, Hung,Stankeviciute, Gabriele,Tang, Peijun

, (2022/01/06)

The bacterial domain produces numerous t...

Development of an Amino Acid/Hydroxy Oxime Dual Catalyst System for Highly Stereoselective Direct Asymmetric Aldol Reactions in the Presence of Water

Mridha, Moniruzzaman,Ma, Guangning,Palo-Nieto, Carlos,Afewerki, Samson,Cordova, Armando

, p. 383 - 390 (2016/12/24)

An eco-friendly dual catalyst system for...

Divergent total synthesis of D-ribo-phytosphingosine and L-ribo-phytosphingosine from D-ribose

Chun, Jong Soo,Hong, Seung Min,Jeon, Tae Hong,Park, Sook Jin,Son, Han Pyo,Jung, Jun Min,Choi, Young Jae,Kim, In Su,Jung, Young Hoon

, p. 8550 - 8556 (2016/12/09)

Divergent total synthesis of D-ribo-phyt...

Chemo- and Diastereoselective N-Heterocyclic Carbene-Catalyzed Cross-Benzoin Reactions Using N-Boc-α-amino Aldehydes

Haghshenas, Pouyan,Gravel, Michel

supporting information, p. 4518 - 4521 (2016/09/28)

N-Boc-α-amino aldehydes are shown to be ...

554-62-1 Process route

(2S,3S,4R)-2-azido-1,3,4-octadecanetriol
117168-59-9

(2S,3S,4R)-2-azido-1,3,4-octadecanetriol

D-ribo-phytosphingosine
554-62-1

D-ribo-phytosphingosine

Conditions
Conditions Yield
With lithium aluminium tetrahydride; In tetrahydrofuran; 1.) 30 min, RT; 2.) 1 h, reflux;
95%
With hydrogen; palladium on activated charcoal; In methanol; at 20 ℃; for 48h;
94%
With pyridine; hydrogen sulfide; water; Ambient temperature;
87%
With hydrogen sulfide; In pyridine; water; for 168h; Ambient temperature;
87%
With palladium 10% on activated carbon; hydrogen; In methanol; at 25 ℃; for 3h;
87%
With triphenylphosphine; In pyridine; water;
tert-butyl [(2S,3S,4R)-1,3,4-trihydroxyoctadecan-2-yl]carbamate
175696-50-1

tert-butyl [(2S,3S,4R)-1,3,4-trihydroxyoctadecan-2-yl]carbamate

D-ribo-phytosphingosine
554-62-1

D-ribo-phytosphingosine

Conditions
Conditions Yield
With trifluoroacetic acid; In water; at 20 ℃; for 0.5h;
82%
With trifluoroacetic acid; In water; at 20 ℃; for 0.5h; Inert atmosphere;
82%
With trifluoroacetic acid; at 20 ℃; for 0.5h;
43%
With hydrogen cation;
With trifluoroacetic acid; In water; for 0.25h; Ambient temperature;
997 mg
With trifluoroacetic acid; In water; at 20 ℃; for 0.333333h;
With trifluoroacetic acid; In dichloromethane; at 0 - 20 ℃; for 0.75h; enantioselective reaction;
31 mg

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554-62-1 Downstream products

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    1987-40-2

    (2S,3R,4R)-2-(N-benzoyl)amino-octadecane-1,3,4-triol

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    tert-butyl [(2S,3S,4R)-1,3,4-trihydroxyoctadecan-2-yl]carbamate

  • 117168-59-9
    117168-59-9

    (2S,3S,4R)-2-azido-1,3,4-octadecanetriol

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    111149-09-8

    N-palmitoyl-D-ribo-phytosphingosine