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Lineare Formel:
NH2COCH2CH(NH2)COOH · H2O
CAS-Nummer:
Molekulargewicht:
150.13
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352209
EC Number:
200-735-9
MDL number:
Beilstein/REAXYS Number:
1723527
Technischer Dienst
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Unterstützung erhaltenProduktname
biological source
synthetic
Quality Segment
assay
≥99% (TLC)
form
powder
color
white to off-white
mp
233-235 °C (lit.)
application(s)
cell analysis
peptide synthesis
SMILES string
[H]O[H].N[C@@H](CC(N)=O)C(O)=O
InChI
1S/C4H8N2O3.H2O/c5-2(4(8)9)1-3(6)7;/h2H,1,5H2,(H2,6,7)(H,8,9);1H2/t2-;/m0./s1
InChI key
RBMGJIZCEWRQES-DKWTVANSSA-N
General description
Asparagine biosynthesis is catalyzed by glutamine-dependent asparagine synthetase in mammalian tissues. Elevated levels of free asparagine is observed in plants facing stress in the form of drought or high salt. It is also present in senescing leaves and germinating seeds.
Application
L-Asparagine monohydrate has been used:
- as a component of Sauton′s and chelated Sauton′s media for mycobacterial growth
- to test its effect in the induction of Ca2+ flux in rice roots using aequorin luminescence imaging
- as a component of fermentation medium for the Blakeslea trispora spores
Biochem/physiol Actions
L-Asparagine, a proteinogenic amino acid, is used in biomanufacturing cell culture systems for the production of therapeutic recombinant proteins and monoclonal antibodies and in cell culture based research.
Asparagine has high nitrogen to carbon ratio and is a key regulator for nitrogen storage and transport. Its thermal degradation in the presence of sugars leads to the acrylamide formation in foods. Asparagine serves as an amino acid exchange factor and is essential for amino acid homeostasis. It favors cancer cell proliferation.
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11 - Combustible Solids
Was ist los?
WGK 1
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
PSA (Persönliche Schutzausrüstung)
Eyeshields, Gloves, type N95 (US)
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