ChemicalBook--->CAS DataBase List--->1783-96-6

1783-96-6

1783-96-6 Structure

1783-96-6 Structure
IdentificationMore
[Name]

D-Aspartic acid
[CAS]

1783-96-6
[Synonyms]

D-2-AMINOBUTANEDIOIC ACID
D-AMINOSUCCINIC ACID
D-ASP
D-ASPARAGINIC ACID
D-(-)-ASPARTIC ACID
D-ASPARTIC ACID
H-D-ASP-OH
(R)-2-AMINOSUCCINIC ACID
(R)-(-)-AMINOSUCCINIC ACID
(R)-AMINOSUCCINIC ACID
(R)-(-)-ASPARTIC ACID
1-Amino-1,2-carboxyethane
d-aspartic
d-asparticaci
l-Asparagic acid
(R)-(-)-Aminosuccinic acid(R)-2-Aminosuccinic acid
D-ASPARTIC ACID CRYSTALLINE
D0001H-D-Asp-Oh
D-Aminosuccinicacid=H-D-Asp-OH
D(-)-Aspartic acid, 99+%
[EINECS(EC#)]

217-234-6
[Molecular Formula]

C4H7NO4
[MDL Number]

MFCD00063081
[Molecular Weight]

133.1
[MOL File]

1783-96-6.mol
Chemical PropertiesBack Directory
[Appearance]

White or almost white crystalline powder
[Melting point ]

>300 °C(lit.)
[alpha ]

-25.8 º (c=5, 5N HCl)
[Boiling point ]

245.59°C (rough estimate)
[density ]

1.66
[refractive index ]

-25 ° (C=8, 50% HCl)
[storage temp. ]

Store at RT.
[solubility ]

Aqueous Acid (Sparingly)
[form ]

Crystalline Powder
[pka]

pK1: 1.89(0);pK2: 3.65;pK3: 9.60 (25°C)
[color ]

White to off-white
[Optical Rotation]

[α]20/D 24°, c = 2.3 in 6 M HCl
[Water Solubility ]

SOLUBLE
[Detection Methods]

T,NMR,Rotation
[Merck ]

14,840
[BRN ]

1723529
[InChI]

1S/C4H7NO4/c5-2(4(8)9)1-3(6)7/h2H,1,5H2,(H,6,7)(H,8,9)/t2-/m1/s1
[InChIKey]

CKLJMWTZIZZHCS-UWTATZPHSA-N
[SMILES]

N[C@H](CC(O)=O)C(O)=O
[LogP]

-1.075 (est)
[CAS DataBase Reference]

1783-96-6(CAS DataBase Reference)
[NIST Chemistry Reference]

D-aspartic acid(1783-96-6)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xn
[Risk Statements ]

R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S24/25:Avoid contact with skin and eyes .
S36:Wear suitable protective clothing .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
[WGK Germany ]

3
[RTECS ]

CI9097500
[HS Code ]

29224900
[Storage Class]

11 - Combustible Solids
Raw materials And Preparation ProductsBack Directory
[Raw materials]

dimethyl L-aspartate
[Preparation Products]

(R)-(+)-1-Boc-3-aminopyrrolidine-->(R)-3-(Boc-amino)pyrrolidine-->3-oxopropanoic acid-->N-Acetyl-D-aspartic acid-->D-Aspartic acid, 1,4-diethyl ester-->Fmoc-D-Aspartic acid-4-methyl ester
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

D-Aminosuccinic acid(1783-96-6).msds
Hazard InformationBack Directory
[Chemical Properties]

White or almost white crystalline powder
[Uses]

A non-essential amino acid found in food sources and dietary supplements. D-Aspartic acid's conjugate base D-aspartate has potential use as a a therapeutic agent in the treatment of schizophrenia-related symptoms.
[Application]

Dietary inclusion of barley sprout, D-Aspartic acid, or their combination have a potential to improve various aspects of reproductive performance in aging roosters[2].
[Definition]

ChEBI: The D-enantiomer of aspartic acid.
[reaction suitability]

reaction type: solution phase peptide synthesis
[Biological Activity]

Endogenous NMDA receptor agonist with similar activity to the L-isomer (L-Aminosuccinic acid ). Also a non-metabolizable substrate for EAA uptake systems. Modulates melatonin synthesis in the pineal gland.
[Synthesis]

dimethyl L-aspartate

6384-18-5

D-Aspartic acid

1783-96-6

In a reaction vessel, 4.85 g (0.03 mol) of dimethyl (S)-2-aminosuccinate was added to 50 mL of 6 M potassium hydroxide solution and the hydrolysis reaction was carried out by heating and refluxing for 3 hrs. Upon completion of the reaction, the pH of the reaction solution was adjusted to 6.5 with 6 N hydrochloric acid.The reaction solution was purified by passing it through a regenerated cation exchange resin column and the effluent with pH=4 was collected. The collected effluent was concentrated under reduced pressure to one-fifth of the original volume and then precipitated by adding 95% methanol. The precipitate was collected by filtration and dried to give 3.3 g of D-aspartic acid in 82.5% yield.

[storage]

Room temperature
[References]

[1] Patent: CN105503628, 2016, A. Location in patent: Paragraph 0026
Spectrum DetailBack Directory
[Spectrum Detail]

D-Aspartic acid(1783-96-6)1HNMR
D-Aspartic acid(1783-96-6)IR1
D-Aspartic acid(1783-96-6)IR2
D-Aspartic acid(1783-96-6)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

D(-)-Aspartic acid, 99+%(1783-96-6)
[Alfa Aesar]

D-Aspartic acid, 99%(1783-96-6)
[Sigma Aldrich]

1783-96-6(sigmaaldrich)
[TCI AMERICA]

D-Aspartic Acid,>98.0%(T)(1783-96-6)
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