Aminomalonicacid structure, CAS 1068-84-4

Aminomalonicacid

CAS Number1068-84-4

SynonymsAminomalonic acid; 2-aminopropanedioic acid; aminopropanedioic acid

Molecular FormulaC3H5NO4

Molecular Weight119.08

Purity

Density1.7±0.1 g/cm3

Boiling Point402.6±40.0 °C at 760 mmHg

Melting Point240-245°C

Flash Point

Appearance

EINECS

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Symbol

Signal Word

Cat. No.: 2A-9076221 Purity:
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Chemical & Physical Properties
CAS Number1068-84-4
Catalog No.2A-9076221
Chinese Name氨基丙二酸
SynonymsAminomalonic acid; 2-aminopropanedioic acid; aminopropanedioic acid
Molecular FormulaC3H5NO4
Molecular Weight119.08
Density1.7±0.1 g/cm3
Boiling Point402.6±40.0 °C at 760 mmHg
Melting Point240-245°C
Storage Conditionroom temperature, dry
ApplicationAminomalonic acid is an amino endogenous metabolite that acts as a highly potent inhibitor of L-asparagine synthase derived from Leukemia 5178Y/AR and mouse pancreas in vitro (Leukemia 5178Y/AR: Ki =
HTC2922499990
PubChem ID4129
SMILESNC(C(=O)O)C(=O)O
InChIInChI=1S/C3H5NO4/c4-1(2(5)6)3(7)8/h1H,4H2,(H,5,6)(H,7,8)
InChI KeyJINBYESILADKFW-UHFFFAOYSA-N
Use ofAminomalonic acid is an amino endogenous metabolite, acts as a strong inhibitor of L-asparagine synthetase from Leukemia 5178Y/AR (Ki= 0.0023 M) and mouse pancreas (Ki= 0.0015 M) in vitro. Aminomalonic acid is a potential biomarker to discriminate between different stages of melanoma metastasis[1][2][3]. Properties Name aminomalonic acid Synonym More Synonyms Aminomalonic acid Biological Activity Description Aminomalonic acid is an amino endogenous metabolite, acts as a strong inhibitor of L-asparagine synthetase from Leukemia 5178Y/AR (Ki= 0.0023 M) and mouse pancreas (Ki= 0.0015 M) in vitro. Aminomalonic acid is a potential biomarker to discriminate between different stages of melanoma metastasis[1][2][3]. Related Catalog Research Areas >> Cancer Ki: 0.0023 M (L-asparagine synthetase from Leukemia 5178Y/AR), 0.0015 M (L-asparagine synthetase from mouse pancreas)[2] References [1]. Van Buskirk JJ, et al. Aminomalonic acid: identification in Escherichia coli and atherosclerotic plaque. Proc Natl Acad Sci U S A. 1984 Feb;81(3):722-5. [2]. Milman HA, et al. Aminomalonic acid and its congeners as potential in vivo inhibitors of L-asparagine synthetase. Enzyme. 1979;24(1):36-47. [3]. Kim HY, et al. Discovery of potential biomarkers in human melanoma cells with different metastatic potential by metabolic and lipidomic profiling. Sci Rep. 2017 Aug 18;7(1):8864. Chemical & Physical Properties Molecular Formula C3H5NO4 Exact Mass 119.021858 PSA 100.62000 LogP -0.27 Index of Refraction 1.545 InChIKey JINBYESILADKFW-UHFFFAOYSA-N SMILES NC(C(=O)O)C(=O)O Safety Information Hazard Codes Xi HS Code 2922499990 Synthetic Route DL-Glutamic aci... Aminomalonic ac... DL-Aspartic Aci... Literature: Tetrahedron Letters, , vol. 24, # 44 p. 4839 - 4842 DL-Alanine Aminomalonic ac... (2S)-2-amino-3-... Literature: Tetrahedron Letters, , vol. 24, # 44 p. 4839 - 4842 DL-Methionine Aminomalonic ac... cysteic acid 13100-82-8 2-Amino-3-metha... 88547-35-7 Literature: Tetrahedron Letters, , vol. 24, # 44 p. 4839 - 4842 Precursor & DownStream Precursor 10 CAS#:40885-82-3 2-(2-PHENYLHYDR... CAS#:6829-41-0 DIETHYL ISONITR... CAS#:62009-47-6 2-Aminomalonamide CAS#:600-33-9 chloromalonic acid DownStream 3 CAS#:473-90-5 Oxomalonic acid CAS#:56-40-6 CAS#:55327-87-2 Acetamidomaloni...
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