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About This Item
Empirical Formula (Hill Notation):
C10H22O5S2
CAS Number:
Molecular Weight:
286.41
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12352201
EC Number:
217-728-1
MDL number:
InChI key
BTOYCPDACQXQRS-LURQLKTLSA-N
InChI
1S/C10H22O5S2/c1-3-16-10(17-4-2)9(15)8(14)7(13)6(12)5-11/h6-15H,3-5H2,1-2H3/t6-,7-,8+,9-/m1/s1
SMILES string
CCSC(SCC)C(O)C(O)C(O)C(O)CO
storage temp.
2-8°C
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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Ryoko Iwamoto et al.
Biochimica et biophysica acta, 1647(1-2), 310-314 (2003-04-11)
The complete amino acid sequence of the D-glucosaminate dehydratase (GADH) alpha-subunit from Pseudomonas fluorescens was determined by PCR using genomic DNA from P. fluorescens as a template. The alpha-subunit comprises 320 amino acids and has a molecular mass of about
R Iwamoto et al.
Bioscience, biotechnology, and biochemistry, 59(3), 408-411 (1995-03-01)
When D-glucosaminate dehydratase (GADH) was incubated with D-glucosaminate (GlcNA) in veronal buffer (VB; 0.01 M, pH 8.0), GlcNA was converted stoichiometrically to glyceraldehyde, pyruvate, and ammonia (aldolase reaction A). This reaction occurred in addition to the dehydratase reaction (conversion of
Wei-Wei Duan et al.
Huan jing ke xue= Huanjing kexue, 33(1), 26-31 (2012-03-29)
The aim was to compare the characteristics and the differences in carbon catabolic diversity of air samples collected from five locations that around the edge of Taklamakan desert. The characteristics and the differences of carbon metabolic profiles were detected by
Sheng-Ju Ou et al.
Archiv der Pharmazie, 339(9), 527-530 (2006-08-31)
Two chromium(III) complexes of glucosaminic acid were synthesized by neutralization and exchange reaction. The formation of 1 : 1 and 2 : 3 (Cr : glucosaminate) complexes was confirmed by elemental analyses and spectroscopic studies. The effect of the complexes
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