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Key Documents

74089

Sigma-Aldrich

1-Amino-1-deoxy-scyllo-inositol

≥95.0% (TLC)

Synonym(s):

scyllo-Inosamine

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About This Item

Empirical Formula (Hill Notation):
C6H13NO5
CAS Number:
Molecular Weight:
179.17
Beilstein:
2802457
UNSPSC Code:
12352201
PubChem Substance ID:

Quality Level

Assay

≥95.0% (TLC)

form

powder

storage temp.

2-8°C

SMILES string

O[C@@H]1[C@@H](N)[C@H](O)[C@@H](O)[C@H](O)[C@H]1O

InChI

1S/C6H13NO5/c7-1-2(8)4(10)6(12)5(11)3(1)9/h1-6,8-12H,7H2/t1-,2-,3+,4+,5-,6-

InChI key

JXAOTICXQLILTC-CDRYSYESSA-N

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.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Kenichi Yokoyama et al.
Journal of the American Chemical Society, 127(16), 5869-5874 (2005-04-21)
The doubly functional aminotransferase BtrS in the 2-deoxystreptamine (DOS) biosynthesis, in which two transaminations are involved, was characterized by a genetic as well as a chemical approach with the heterologously expressed enzyme. The gene disruption study clearly showed that BtrS
Lucía Díaz et al.
Journal of medicinal chemistry, 54(7), 2069-2079 (2011-03-05)
A library of aminocyclitols derived from CuAAC reaction between N-propargylaminocyclitol 4 and a series of azides [1-25] is described and tested against GCase. Azides have been chosen from a large collection of potential candidates that has been filtered according to
Meritxell Egido-Gabás et al.
Organic & biomolecular chemistry, 3(7), 1195-1201 (2005-03-24)
A series of 13 aminocyclitol derivatives belonging to two different families is described. Their configuration is governed by the regio- and stereocontrolled epoxide opening of a suitably protected conduritol-B epoxide. Studies on several glycosyl processing enzymes indicate that some of
Christopher P Phenix et al.
Chembiochem : a European journal of chemical biology, 9(10), 1591-1602 (2008-06-07)
MosA is an enzyme from Sinorhizobium meliloti L5-30, a beneficial soil bacterium that forms a symbiotic relationship with leguminous plants. MosA was proposed to catalyze the conversion of scyllo-inosamine to 3-O-methyl-scyllo-inosamine (compounds known as rhizopines), despite the MosA sequence showing
C P Saint et al.
Journal of bacteriology, 175(16), 5205-5215 (1993-08-01)
Rhizopines are selective growth substrates synthesized in nodules only by strains of rhizobia capable of their catabolism. We report the isolation and study of genes for the synthesis and catabolism of a new rhizopine, scyllo-inosamine (sIa), from alfalfa nodules induced

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