A9006
DL-Aspartic acid
≥99% (TLC)
Sinónimos:
(±)-2-Aminosuccinic acid
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Fórmula lineal:
HOOCCH2CH(NH2)COOH
Número CAS:
Peso molecular:
133.10
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352209
EC Number:
210-513-3
MDL number:
Beilstein/REAXYS Number:
774618
Servicio técnico
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Permítanos ayudarleNombre del producto
DL-Aspartic acid, ≥99% (TLC)
Quality Level
assay
≥99% (TLC)
form
powder
color
white
mp
>300 °C (lit.)
solubility
1 M HCl: soluble
application(s)
cell analysis
peptide synthesis
SMILES string
NC(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)
InChI key
CKLJMWTZIZZHCS-UHFFFAOYSA-N
Biochem/physiol Actions
DL-Aspartic acid (DL-Asp) is a racemic mixture of the proteinogenic amino acid L-aspartate and the non-proteinogenic amino acid D-aspartate. DL-Aspartic acid is used in studies on factors and conditions that enhance semen and sperm quality.
Clase de almacenamiento
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Jannick Jacobsen et al.
Dalton transactions (Cambridge, England : 2003), 48(23), 8433-8441 (2019-05-23)
Six different chiral and achiral alkane dicarboxylic C4-acids, i.e. succinic acid (H2SUC), dl-2-methylsuccinic acid (H2MS), 2,3-dimethylsuccinic acid (H2DMS) and aspartic acid (d-, l- and dl-H2ASP), were used to obtain Ce(iv)-MOFs via microwave assisted reactions. In water-based syntheses, MOFs with three
Xiong Deng et al.
Biochimica et biophysica acta, 1851(12), 1521-1529 (2015-09-04)
In hyperinsulinemic states including obesity and T2DM, overproduction of fatty acid and triglyceride contributes to steatosis of the liver, hyperlipidemia and hepatic insulin resistance. This effect is mediated in part by the transcriptional regulator sterol responsive element binding protein-1c (SREBP-1c)
John Malysz et al.
Journal of visualized experiments : JoVE, (155) (2020-02-18)
Detrusor smooth muscle (DSM) cells present within the urinary bladder wall ultimately facilitate urine storage and voiding. Preparation of the viable, fresh, and isolated DSM cells presents an important technical challenge whose achievement provides optimal cells for subsequent functional and