Your Location:Home >Products >API >80-78-4

80-78-4

  • Product Name:Solanidine
  • Molecular Formula:C27H43 N O
  • Molecular Weight:397.645
Inquiry

Product Details

pd_meltingpoint:212-214°C

Purity:99%

Reputable factory supply Solanidine 80-78-4 in stock with high standard

  • Molecular Formula:C27H43 N O
  • Molecular Weight:397.645
  • Vapor Pressure:3.13E-12mmHg at 25°C 
  • Melting Point:212-214°C 
  • Boiling Point:503.1°C at 760 mmHg 
  • Flash Point:223.5°C 
  • PSA:23.47000 
  • Density:1.1g/cm3 
  • LogP:5.59290 

SOLANIDINE(Cas 80-78-4) Usage

Purification Methods

Solanidine crystallises from CHCl3/MeOH, aqueous EtOH or aqueous MeOH as needles. TLC on Al2O3 plates using CH2Cl2/MeOH (98:2) gives a spot at RF 0.47. The hydrochloride crystallises from aqueous EtOH with m 345o(dec). The acetate crystallises from EtOH with m 208o. [Schreiber & Roensch Tetrahedron 21 6451965, Kessar et al. Tetrahedron 27 2153 1971, Reichestein & Reich Ann Rev Biochem 15 155 1946, Beilstein 21 III/IV 1398, 27 III/IV 2000.]

InChI:InChI=1/C27H43NO/c1-16-5-8-23-17(2)25-24(28(23)15-16)14-22-20-7-6-18-13-19(29)9-11-26(18,3)21(20)10-12-27(22,25)4/h6,16-17,19-25,29H,5,7-15H2,1-4H3

80-78-4 Relevant articles

-

Kitajima,J.,Komori,T.

, p. 187 (1982)

-

Divergent Synthesis of Solanidine and 22-epi-Solanidine

Hou, Ling-Li,Shi, Yong,Zhang, Zhi-Dan,Wu, Jing-Jing,Yang, Qing-Xiong,Tian, Wei-Sheng

, p. 7463 - 7469 (2017)

A divergent synthesis of solanidine and ...

Asymmetric synthesis of (-)-solanidine and (-)-tomatidenol

Chen, Fen-Er,Huang, Guanxin,Shi, Yong,Tian, Wei-Sheng,Wang, Yun,Zhuang, Chunlin

, p. 3169 - 3176 (2020)

A concise asymmetric synthesis of two na...

Synthesis of Demissidine and Solanidine

Zhang, Zhi-Dan,Shi, Yong,Wu, Jing-Jing,Lin, Jing-Rong,Tian, Wei-Sheng

supporting information, p. 3038 - 3040 (2016/07/06)

Demissidine and solanidine, two steroida...

Metabolism of the potato saponins α-chaconine and α-solanine by Gibberella pilicaris

Weltring, Klaus-M,Wessels, Judith,Geyer, Rudolf

, p. 1005 - 1009 (2007/10/03)

Potato tubers accumulate varying amounts...

80-78-4 Process route

β-Chaconine
469-14-7

β-Chaconine

β-D-glucose
492-61-5

β-D-glucose

β-L-rhamnose
6155-36-8

β-L-rhamnose

Solanidine
80-78-4,566-09-6,7050-47-7,19330-99-5,76703-36-1

Solanidine

Conditions
Conditions Yield
With hydrogenchloride; In ethanol; at 100 ℃; for 3h; Product distribution;
With hydrogenchloride; In ethanol; at 100 ℃; for 3h;
Stenanthine
80248-79-9

Stenanthine

β-D-glucose
492-61-5

β-D-glucose

β-L-rhamnose
6155-36-8

β-L-rhamnose

Solanidine
80-78-4,566-09-6,7050-47-7,19330-99-5,76703-36-1

Solanidine

Conditions
Conditions Yield
With hydrogenchloride; In ethanol; at 100 ℃; Product distribution;

80-78-4 Upstream products

  • 81942-09-8
    81942-09-8

    solanidine 3-O-α-L-rhamnopyranosyl-(1<*>2)-O-<β-D-glucopyranosyl-(1<*>4)>-β-D-glucopyranoside

  • 472-51-5
    472-51-5

    solanidine 3-O-α-L-rhamnopyranosyl-(1->2)-β-D-glucopyranoside

  • 78720-01-1
    78720-01-1

    C30H47NO5S

  • 20562-03-2
    20562-03-2

    α-chaconine

80-78-4 Downstream products

  • 160381-26-0
    160381-26-0

    3β(p-toluenesulfonyloxy)-22αH,25βH-solanid-5-en-3-ol

  • 474-08-8
    474-08-8

    demissidine

  • 160381-27-1
    160381-27-1

    3α,5-cyclo-5α,22αH,25βH-solanidan-6β-ol

  • 511-37-5
    511-37-5

    solanidine β-D-galactopyranoside

Relevant Products