A9256
L-Aspartic acid
≥98% (HPLC)
Synonym(s):
(S)-(+)-Aminosuccinic acid, (S)-Aminobutanedioic acid
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About This Item
Linear Formula:
HO2CCH2CH(NH2)CO2H
CAS Number:
Molecular Weight:
133.10
NACRES:
NA.26
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
EC Number:
200-291-6
MDL number:
Beilstein/REAXYS Number:
1723530
Product Name
L-Aspartic acid, reagent grade, ≥98% (HPLC)
grade
reagent grade
Quality Level
assay
≥98% (HPLC)
form
powder, crystals or chunks
color
white to off-white
mp
>300 °C (dec.) (lit.)
solubility
H2O: 5 mg/mL, 0.5 M HCl: 50 mg/mL (with heat), 1 M NaOH: 50 mg/mL
SMILES string
N[C@@H](CC(O)=O)C(O)=O
InChI
1S/C4H7NO4/c5-2(4(8)9)1-3(6)7/h2H,1,5H2,(H,6,7)(H,8,9)/t2-/m0/s1
InChI key
CKLJMWTZIZZHCS-REOHCLBHSA-N
Gene Information
human ... CA1(759), CA2(760)
rat ... Grin2a(24409)
Application
L-aspartic acid has been used as one of the components of synthetic drop out media for culturing budding yeast. It has also been used to study non-enzymatic gluconeogenesis.
Biochem/physiol Actions
Aspartic acid is a non-essential amino acid. It is involved in the Urea cycle, Krebs cycle and in DNA metabolism.
Principal neurotransmitter for fast synaptic excitation.
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Storage Class
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Eric R. Braverman
The Healing Nutrients Within: Facts, Findings, and New Research on Amino Acids, 1-504 (2007)
Method for Multiplexing CRISPR/Cas9 in Saccharomyces cerevisiae Using Artificial Target DNA Sequences
Rachael M. Giersch and Gregory C. Finnigan
Bio-protocol, 7(18), 1-24 (2017)
Nonenzymatic gluconeogenesis-like formation of fructose 1,6-bisphosphate in ice.
Messner CB
Proceedings of the National Academy of Sciences of the USA, 114(28), 7403-7407 (2017)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| A9256-100G | 04061835366156 |
| A9256-1G | 04061823760232 |
| A9256-1KG | 04061833401637 |
| A9256-500G | 04061833401644 |
| A9256-5KG | 04061832720623 |