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D-Serine

CAS 312-84-5 ≥95%

D-Serine | CAS 312-84-5 | ≥95%

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Technical Specifications

CAS Number 312-84-5
EC / EINECS Number 206-229-4
MDL Number MFCD00004269
SMILES C([C@H](C(=O)O)N)O
InChI InChI=1S/C3H7NO3/c4-2(1-5)3(6)7/h2,5H,1,4H2,(H,6,7)/t2-/m1/s1
InChIKey MTCFGRXMJLQNBG-UWTATZPHSA-N
PubChem CID 71077
Molecular Formula C₃H₇NO₃
Molecular Weight 105.09 g/mol
Melting Point 229–233 °C (dec.)
Solubility Soluble in water (346 g/L at 20 °C) and in mineral acids; insoluble in ethanol, diethyl ether and benzene
Purity ≥95%
Physical Form White crystalline powder
HS Code 2922.50
Shelf Life Retest period: 36 months from date of manufacture
Storage Conditions Keep tightly closed in a cool, dry, dark place. Recommended temperature: (<15 °C)

Product Description & Scientific Applications

D-Serine is the endogenous co-agonist of the NMDA receptor: a free d-amino acid enriched in the mammalian brain throughout life, where peripheral tissues and blood contain only low or trace levels.

NMDA receptor co-agonist. It binds the glycine-regulatory site stereoselectively and stimulates it more potently than glycine itself, with affinity and ED50 in the high nanomolar range. Selective enzymatic degradation identified it as the principal endogenous co-agonist of synaptic NMDA receptors at mature excitatory synapses of the prefrontal cortex, and it is the primary co-agonist at mature forebrain synapses generally — the physiological co-agonist required for synaptic plasticity.

The two enzymes that set the level. Cytosolic serine racemase converts l-serine to d-serine; peroxisomal d-amino acid oxidase degrades it. Upstream, blocking astrocytic 3-phosphoglycerate dehydrogenase suppresses de novo synthesis and reduces both NMDA receptor potentials and long-term potentiation at the Schaffer collateral–CA1 synapse.

Applications

  • Preventing glycine-dependent desensitisation in NMDA receptor recordings
  • d-amino acid oxidase assay substrate
  • Serine palmitoyltransferase inhibition
  • Bacterial spore germination studies
  • Chiral intermediate in pharmaceutical synthesis

Shipping Destinations

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  • Worldwide: 7–14 business days, selected locations.

Safety Information

Hazard Class Not regulated for transport
Transport Category Not classified as dangerous goods for transport (ADR/IATA/IMDG)
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