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Merck
CN

A5625

N-Acetyl-DL-aspartic acid

≥95%

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关于此项目

经验公式(希尔记法):
C6H9NO5
化学文摘社编号:
分子量:
175.14
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.26
EC Number:
219-827-5
MDL number:
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产品名称

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



存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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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



全球贸易项目编号

货号GTIN
A5625-5G04061832421155