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N8143

Sigma-Aldrich

Neocarradodecaose 41,43,45,47,49,411-hexasulfate hexasodium salt

≥95%

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About This Item

Formula condensata:
C72H104O73S6Na6
Numero CAS:
133628-77-0
Peso molecolare:
2467.88
Numero MDL:
MFCD00133661
Codice UNSPSC:
12352201
ID PubChem:
329818679

Saggio

≥95%

Forma fisica

solid

Temperatura di conservazione

2-8°C

Stringa SMILE

[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O[C@H]2O[C@@H]3CO[C@H]([C@H]2O)[C@H]3O[C@@H]4O[C@H](CO)[C@H](OS([O-])(=O)=O)[C@H](O[C@H]5O[C@@H]6CO[C@H]([C@H]5O)[C@H]6O[C@@H]7O[C@H](CO)[C@H](OS([O-])(=O)=O)[C@H](O[C@H]8O[C@@H]9CO[C@H]([C@H]8O)[C@H]9O[C@@H]%10O[C@H](CO)[C@H](OS([O-])(=O)=O)[C@H](O[C@H]%11O[C@@H]%12CO[C@H]([C@H]%11O)[C@H]%12O[C@@H]%13O[C@H](CO)[C@H](OS([O-])(=O)=O)[C@H](O[C@H]%14O[C@@H]%15CO[C@H]([C@H]%14O)[C@H]%15O[C@@H]%16O[C@H](CO)[C@H](OS([O-])(=O)=O)[C@H](O[C@H]%17O[C@@H]%18CO[C@@H]([C@H]%18O)[C@H]%17O)[C@H]%16O)[C@H]%13O)[C@H]%10O)[C@H]7O)[C@H]4O)[C@H]1OS([O-])(=O)=O

InChI

1S/C72H110O73S6.6Na/c73-1-13-43(140-146(93,94)95)55(26(80)61(92)117-13)134-63-28(82)50-38(20(124-63)8-112-50)129-69-34(88)57(45(15(3-75)119-69)142-148(99,100)101)136-65-30(84)52-40(22(126-65)10-114-52)131-71-36(90)59(47(17(5-77)121-71)144-150(105,106)107)138-67-32(86)54-42(24(128-67)12-116-54)133-72-37(91)60(48(18(6-78)122-72)145-151(108,109)110)139-66-31(85)53-41(23(127-66)11-115-53)132-70-35(89)58(46(16(4-76)120-70)143-149(102,103)104)137-64-29(83)51-39(21(125-64)9-113-51)130-68-33(87)56(44(14(2-74)118-68)141-147(96,97)98)135-62-27(81)49-25(79)19(123-62)7-111-49;;;;;;/h13-92H,1-12H2,(H,93,94,95)(H,96,97,98)(H,99,100,101)(H,102,103,104)(H,105,106,107)(H,108,109,110);;;;;;/q;6*+1/p-6/t13-,14-,15-,16-,17-,18-,19-,20-,21-,22-,23-,24-,25+,26-,27-,28-,29-,30-,31-,32-,33-,34-,35-,36-,37-,38+,39+,40+,41+,42+,43+,44+,45+,46+,47+,48+,49+,50-,51-,52-,53-,54-,55-,56-,57-,58-,59-,60-,61-,62-,63-,64-,65-,66-,67-,68+,69+,70+,71+,72+;;;;;;/m1....../s1
YWSHUIVBCLNTEM-GGOYDXLKSA-H

Applicazioni

Neocarradodecaose has been used in a study to assess ionization and mass spectrometry of sulfated neocarrabiose oligosaccharides. It has also been used in a study to investigate ionic liquid matrixes optimized for MALDI-MS.

Altre note

Mixed anomers

Nota sulla preparazione

Prepared enzymatically from κ-carrageenan.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (COA)

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Yuko Fukuyama et al.
Analytical chemistry, 80(6), 2171-2179 (2008-02-16)
1,1,3,3-tetramethylguanidium (TMG) salt of alpha-cyano-4-hydroxycinnamic acid (CHCA) (G(2)CHCA) was reported by Tatiana et al. as a useful ionic liquid matrix (ILM) for sulfated oligosaccharides to suppress the loss of sulfate groups. However, the report mainly referred to positive ion spectra
Yuko Fukuyama et al.
Carbohydrate research, 337(17), 1553-1562 (2002-09-28)
Several commercial sulfated neocarrabiose oligosaccharides were analyzed by matrix-assisted ultraviolet laser-desorption ionization time-of-flight mass spectrometry (UV-MALDI-TOF-MS). UV-MALDI-TOF-MS was carried out in the linear and reflectron modes and, as routine, in both the positive- and negative-ion modes. 2,5-Dihydroxybenzoic acid and nor-harmane
M W McLean et al.
European journal of biochemistry, 93(3), 553-558 (1979-02-01)
A kappa-carrageenase was isolated from the cell-free medium of cultured Pseudomonas carrageenovora. From dodecylsulphate/polyacrylamide gel electrophoresis, a single protein (identified as the kappa-carrageenase) was detected in the medium. Activity against nominal carrageenan types and inspection of the products indicate the

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