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A1330000

Ácido L-aspártico

European Pharmacopoeia (EP) Reference Standard

Sinónimos:

Ácido (S)-(+)-aminosuccínico, Ácido (S-aminobutanodioico

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About This Item

Fórmula lineal:
HO2CCH2CH(NH2)CO2H
Número de CAS:
56-84-8
Peso molecular:
133.10
Beilstein:
1723530
Número MDL:
MFCD00002616
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
329770359
NACRES:
NA.24

grado

pharmaceutical primary standard

familia API

aspartic acid

fabricante / nombre comercial

EDQM

mp

>300 °C (dec.) (lit.)

aplicaciones

pharmaceutical (small molecule)

formato

neat

temp. de almacenamiento

2-8°C

cadena SMILES

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

InChI

1S/C4H7NO4/c5-2(4(8)9)1-3(6)7/h2H,1,5H2,(H,6,7)(H,8,9)/t2-/m0/s1

Clave InChI

CKLJMWTZIZZHCS-REOHCLBHSA-N

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Descripción general

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.

Aplicación

Aspartic acid EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.

Acciones bioquímicas o fisiológicas

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Envase

The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.

Otras notas

Sales restrictions may apply.

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Referencia del producto
Descripción
Precios

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 1

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Choose from one of the most recent versions:

Certificados de análisis (COA)

Lot/Batch Number

Sorry, we don't have COAs for this product available online at this time.

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(S)-(+)-Aspartic acid for synthesis

Sigma-Aldrich

8.16003

(S)-(+)-Aspartic acid

D-Aspartic acid ReagentPlus®, 99%

Sigma-Aldrich

219096

D-Aspartic acid

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C3290000

L-cisteína hydrochloride monohydrate

Alanine European Pharmacopoeia (EP) Reference Standard

A0325000

Alanine

L-Asparragina monohydrate European Pharmacopoeia (EP) Reference Standard

Y0000305

L-Asparragina monohydrate

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USP

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Serine European Pharmacopoeia (EP) Reference Standard

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Serine

M J Collins et al.
Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 354(1379), 51-64 (1999-03-26)
The increase in proportion of the non-biological (D-) isomer of aspartic acid (Asp) relative to the L-isomer has been widely used in archaeology and geochemistry as a tool for dating. the method has proved controversial, particularly when used for bones.
R A Azevedo et al.
Amino acids, 30(2), 143-162 (2006-03-10)
Aspartate is the common precursor of the essential amino acids lysine, threonine, methionine and isoleucine in higher plants. In addition, aspartate may also be converted to asparagine, in a potentially competing reaction. The latest information on the properties of the
Stefanie Ritz-Timme et al.
Ageing research reviews, 1(1), 43-59 (2002-06-01)
Aspartic acid racemization (AAR) represents one of the major types of non-enzymatic covalent modification that leads to an age-dependent accumulation of abnormal protein in numerous human tissues. In vivo racemization is an autonomic process during the "natural" ageing of proteins
E R Waite et al.
Forensic science international, 103(2), 113-124 (1999-09-11)
Accurate age determination of adult cadavers and human remains is a key requirement in forensic practice. The current morphological methods lack accuracy and precision, require specialist training and are costly. The use of aspartic acid racemization (AAR) in human dentine
Víctor A Lórenz-Fonfría et al.
Biochimica et biophysica acta, 1837(5), 626-642 (2013-11-12)
The new and vibrant field of optogenetics was founded by the seminal discovery of channelrhodopsin, the first light-gated cation channel. Despite the numerous applications that have revolutionised neurophysiology, the functional mechanism is far from understood on the molecular level. An
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