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M3387

Sigma-Aldrich

N-Methyl-L-aspartic acid

Synonym(s):

(S)-2-(Methylamino)succinic acid

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About This Item

Empirical Formula (Hill Notation):
C5H9NO4
CAS Number:
Molecular Weight:
147.13
Beilstein:
2437887
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:

form

powder

color

white

SMILES string

CN[C@@H](CC(O)=O)C(O)=O

InChI

1S/C5H9NO4/c1-6-3(5(9)10)2-4(7)8/h3,6H,2H2,1H3,(H,7,8)(H,9,10)/t3-/m0/s1

InChI key

HOKKHZGPKSLGJE-VKHMYHEASA-N

Gene Information

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Other Notes

Inactive isomer of N-methyl-D-aspartic acid (NMDA).

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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The enzymatic reactions leading to the deamination of β-lysine, lysine, or 2-aminoadipic acid are of great interest for the metabolic conversion of lysine to adipic acid. Enzymes able to carry out these reactions are not known, however ammonia lyases (EC
Watkins, J.C.
Journal of Medicinal and Pharmaceutical Chemistry, 5, 1187-1187 (1962)
Yousuke Tsuneoka et al.
The EMBO journal, 34(21), 2652-2670 (2015-10-02)
Paternal behavior is not innate but arises through social experience. After mating and becoming fathers, male mice change their behavior toward pups from infanticide to paternal care. However, the precise brain areas and circuit mechanisms connecting these social behaviors are

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