N-Acetyl-DL-aspartic acid
Names
[ CAS No. ]:
2545-40-6
[ Name ]:
N-Acetyl-DL-aspartic acid
[Synonym ]:
2-Acetamidosuccinic acid
N-Acetyl aspartic acid
MFCD00066022
Aspartic acid, N-acetyl-
N-Acetyl-DL-aspartic acid
2-acetamidobutanedioic acid
N-Acetyl-DL-aspartic
EINECS 219-827-5
AC-DL-ASPARTIC ACID
acetylaspartic acid
N-Acetylaspartic acid
N-ACETYL-DL-ASPARAGINE
N-acetyl-aspartate
AC-DL-ASN-OH
ACETYL-DL-ASPARAGINE
AC-DL-ASP-OH
Biological Activity
[Description]:
[Related Catalog]:
[In Vitro]
[References]
Chemical & Physical Properties
[ Density]:
1.4±0.1 g/cm3
[ Boiling Point ]:
425.3±35.0 °C at 760 mmHg
[ Molecular Formula ]:
C6H9NO5
[ Molecular Weight ]:
175.139
[ Flash Point ]:
211.0±25.9 °C
[ Exact Mass ]:
175.048065
[ PSA ]:
103.70000
[ LogP ]:
-1.05
[ Vapour Pressure ]:
0.0±2.2 mmHg at 25°C
[ Index of Refraction ]:
1.506
[ Storage condition ]:
2-8°C
MSDS
Safety Information
[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
[ Hazard Codes ]:
Xi
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ HS Code ]:
2924199090
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2924199090
[ Summary ]:
2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%
Articles
J. Biol. Chem. 282 , 23841-53, (2007)
Organic anion transporters (OATs, SLC22) interact with a remarkably diverse array of endogenous and exogenous organic anions. However, little is known about the structural features that determine thei...
Functional changes in the frontal cortex in Parkinson's disease using a rat model.J. Clin. Neurosci. 17 , 628-633, (2010)
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 ...
[Canavan disease or N-acetyl aspartic aciduria: a case report].Arch. Pediatr. 14 , 173-176, (2007)
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 aspartoacy...