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About This Item
Empirical Formula (Hill Notation):
C6H9NO5
CAS Number:
Molecular Weight:
175.14
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.26
EC Number:
219-827-5
MDL number:
Product Name
N-Acetyl-DL-aspartic acid, ≥95%
Quality Level
assay
≥95%
form
powder
color
white to off-white
storage temp.
2-8°C
SMILES string
CC(=O)NC(CC(O)=O)C(O)=O
InChI
1S/C6H9NO5/c1-3(8)7-4(6(11)12)2-5(9)10/h4H,2H2,1H3,(H,7,8)(H,9,10)(H,11,12)
InChI key
OTCCIMWXFLJLIA-UHFFFAOYSA-N
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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Zhongyu Hou et al.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 17(5), 628-633 (2010-02-02)
In recent years, investigations of the pathologic mechanism of Parkinson's disease (PD) have mainly concentrated on the basal ganglia. However, recent studies have confirmed that pathological changes in PD are accompanied by functional motor changes of the cerebral cortex. Rats
J A Harvey et al.
The Biochemical journal, 108(2), 269-274 (1968-06-01)
1. Sample from the neocortex and piriform cortex of guinea pigs and rats were incubated in inulin-containing glucose-saline. Their intracellular (non-inulin) space contained 19-27muequiv. of Na(+)/g. of original tissue. These values were stable between 30 and 100min. after incubation commenced
L Boughamoura et al.
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie, 14(2), 173-176 (2007-01-02)
Canavan disease or N-acetyl aspartic aciduria, is an autosomal recessive leukodystrophy characterized by spongy degeneration of brain. The disease is an inborn error of metabolism caused by aspartoacylase deficiency resulting from accumulation of N-acetyl aspartic acid in the brain. The
Global Trade Item Number
| SKU | GTIN |
|---|---|
| A5625-5G | 04061832421155 |