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Merck
CN

S3375

Sedoheptulose anhydride monohydrate

Synonym(s):

2,7-Anhydro-β-D-altro-heptulopyranose, Sedoheptulosan

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About This Item

Empirical Formula (Hill Notation):
C7H12O6 · H2O
CAS Number:
469-90-9
Molecular Weight:
210.18
NACRES:
NA.25
PubChem Substance ID:
24899556
UNSPSC Code:
12352201
EC Number:
207-424-7
MDL number:
MFCD00150523

Key Documents

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InChI key

TXADMKCMMLBFTL-CQJQEINESA-N

InChI

1S/C7H12O6.H2O/c8-2-7-6(11)5(10)4(9)3(13-7)1-12-7;/h3-6,8-11H,1-2H2;1H2/t3-,4-,5-,6+,7-;/m1./s1

SMILES string

O.[H][C@]12CO[C@](CO)(O1)[C@@H](O)[C@H](O)[C@@H]2O

biological source

Sedum spectabile

form

powder

optical activity

[α]/D -133 to -130 °, c = 2% (w/v) in water

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Preparation Note

Prepared by a modified procedure of LaForge, F.B. and Hudson, C.S., J. Biol. Chem., 30, 61 (1917).

Other Notes

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
020M3802V
020M3802
017K3779V
017K3779
115K3779

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Dauren Biyashev et al.
Annals of the New York Academy of Sciences, 1480(1), 170-182 (2020-09-07)
Injury of the skin from exposure to toxic chemicals leads to the release of inflammatory mediators and the recruitment of immune cells. Nitrogen mustard (NM) and other alkylating agents cause severe cutaneous damage for which there are limited treatment options.

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