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S5006

Sigma-Aldrich

L-Serine O-sulfate potassium salt

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About This Item

Linear Formula:
C3H6NO6SK
CAS Number:
Molecular Weight:
223.25
MDL number:
UNSPSC Code:
12352300
PubChem Substance ID:
NACRES:
NA.23

storage temp.

2-8°C

SMILES string

[K+].N[C@@H](COS([O-])(=O)=O)C(O)=O

InChI

1S/C3H7NO6S.K/c4-2(3(5)6)1-10-11(7,8)9;/h2H,1,4H2,(H,5,6)(H,7,8,9);/q;+1/p-1/t2-;/m0./s1

InChI key

LXIPCUMLLKNUSU-DKWTVANSSA-M

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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J Kunert
Journal of basic microbiology, 25(2), 111-118 (1985-01-01)
The dermatophyte Microsporum gypseum was cultivated on a glucose-arginine medium supplemented with five strongly acidic derivatives of cysteine (L-cysteine sulfinic acid, L-cysteic acid, L-serine-O-sulfate and taurine at a concentration of 5 mmol/l, and L-S-sulfocysteine at a concentration of 2.5 mmol/l).
K J Koller et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 5(11), 2882-2888 (1985-11-01)
[3H]-N-Acetylaspartylglutamate (NAAG) bound saturably and reversibly to crude synaptosomal rat brain membranes. Optimal binding occurred in Tris-HCl buffer, pH 7.2, at 37 degrees C using previously frozen, preincubated membranes. Saturation experiments revealed an apparent KD of 383 +/- 33 nM
H Ueno et al.
Biochemistry, 21(18), 4387-4393 (1982-08-31)
The reaction of serine O-sulfate with cytosolic aspartate aminotransferase [John, R.A., & Fasella, P. (1969) Biochemistry 8, 4477] has been reinvestigated. As in the corresponding reaction with beta-chloroalanine [Morino, Y., Osman, A.M., & Okamoto, M. (1974) J. Biol. Chem. 249
Chizuru Nagayoshi et al.
Protein and peptide letters, 16(2), 201-206 (2009-02-10)
We have successfully expressed an active human brain serine racemase (hSR) with His-tag using moderate halophile. The purified His-hSR showed high elimination and racemization activities on L-serine: the elimination activity was 2.6-fold higher than racemization activity. Both enzyme activities showed
R Contestabile et al.
European journal of biochemistry, 240(1), 150-155 (1996-08-15)
The ability of aspartate aminotransferase to catalyse beta-elimination of alpha-amino acids that have a good leaving group at C beta has been exploited in the synthesis of novel amino acids by the inclusion of appropriate nucleophiles as co-substrates. Two compounds

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