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Home > Encyclopedia > D-Aspartic acid

D-Aspartic acid

pharmaceutical raw materials
D-Aspartic acid structure

D-Aspartic acid 

structure
  • CAS No:

    1783-96-6

  • Formula:

    C4H7NO4

  • Chemical Name:

    D-Aspartic acid

  • Synonyms:

    D-Aspartic acid;Aspartic acid,D-;(-)-Aspartic acid;D-(-)-Aspartic acid;(R)-Aspartic acid;NSC 97922;(2R)-2-Aminobutanedioic acid;(R)-2-Aminosuccinic acid

  • Categories:

    Biochemical Engineering  >  Amino Acids and Derivatives

Description

White or almost white crystalline powderChEBI: The D-enantiomer of aspartic acid.


Solid


D-aspartic acid is the D-enantiomer of aspartic acid. It has a role as a mouse metabolite. It is an aspartic acid and a D-alpha-amino acid. It is a conjugate acid of a D-aspartate(1-). It is an enantiomer of a L-aspartic acid.|The D-isomer of ASPARTIC ACID.

D-Aspartic acid Basic Attributes

133.1

133.10

1723529

217-234-6

4SR0Q8YD1X

DTXSID2045650

29224995

Characteristics

101

-2.8

White to off-white Crystalline Powder

1.66

251 °C

245.59°C (rough estimate)

113.5±24.6 °C

-25 ° (C=8, 50% HCl)

SOLUBLE

Store at RT.

-25.8 º (c=5, 5N HCl)

116.91 Ų [M-H]- [CCS Type: DT, Method: single field calibrated with Agilent tune mix (Agilent)]|121.85 Ų [M-H]- [CCS Type: DT, Method: stepped-field]|120.1 Ų [M-H]-

Safety Information

NONH for all modes of transport

3

20/21/22-36/37/38

24/25-36-26

CI9097500

Xn

Stable under normal temperatures and pressures.

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 7 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

3-hydroxy-N-(2-methyl-1-oxo-2-propenyl)-

D-Aspartic acid Use and Manufacturing

Methods of Manufacturing

In the reaction vessel, Join4.85 g (0.03 mol)D-aspartic acid dimethyl ester, Join6NSodium hydroxide50 ml, Heating hydrolysis for 3 hours, use6NHydrochloric acidPH = 6.5, The reaction solution was passed through a regenerated cation exchange resin column, collectPH = 4Previous effluent, After concentration to a fifth of the original volume under reduced pressure, use95percentEthanol so that precipitation, Filtered and dried to obtain D-aspartic acid3.3 g, yield 82.5percent.

Uses

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

Computed Properties

Molecular Weight:133.10
XLogP3:-2.8
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:133.03750770
Monoisotopic Mass:133.03750770
Topological Polar Surface Area:101
Heavy Atom Count:9
Complexity:133
Defined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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