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Beta-N-oxalylaminoalanine, also known as BOAA, is a naturally occurring neurotoxin found in certain plants, particularly in the genus Lathyrus. It is a non-protein amino acid that can be mistakenly incorporated into proteins during protein synthesis, leading to the disruption of normal cellular functions. BOAA is known to cause a neurological disorder called lathyrism, which is characterized by symptoms such as spastic paraparesis, muscle weakness, and degeneration of the nervous system. The toxin has been associated with outbreaks of lathyrism in regions where Lathyrus sativus, also known as grass pea, is a staple food. The consumption of BOAA-contaminated food can lead to severe health consequences, making it a significant concern in food safety and public health.

7554-89-4

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7554-89-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7554-89-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,5 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7554-89:
(6*7)+(5*5)+(4*5)+(3*4)+(2*8)+(1*9)=124
124 % 10 = 4
So 7554-89-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H8N2O5/c6-1-2(4(9)10)7-3(8)5(11)12/h2H,1,6H2,(H,7,8)(H,9,10)(H,11,12)

7554-89-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-N-oxalyl-2,3-diaminopropanoic acid

1.2 Other means of identification

Product number -
Other names α-N-Oxalyl-diaminopropionsaeure

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7554-89-4 SDS

7554-89-4Downstream Products

7554-89-4Relevant academic research and scientific papers

THE MECHANISM OF THE REARRANGEMENT OF THE NEUROTOXIN β-ODAP TO α-ODAP

Bruyn, Andre De,Becu, Christian,Lambein, Fernand,Kebede, Naod,Abegaz, Berhanu,Nunn, Peter B.

, p. 85 - 90 (1994)

The diketopiperazine suggested to be the intermediate during the spontaneous isomerization of β-ODAP and α-ODAP was synthesized.Its behaviour was studied at selected pH values and provided evidence that its natural occurrence is unlikely. 2-Hydroxy-imidazolidine-2,4-dicarboxylic acid (for the rearrangement β-ODAP α-ODAP) or 2-hydroxy-pyrimidine-2,4-dicarboxylic acid (for the rearrangement γ-ODAB α-ODAB) are suggested to be the unstable intermediates.

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