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335665

Sigma-Aldrich

7-Hydroxycoumarinyl-4-acetic acid

97%

Sinônimo(s):

Umbelliferone-4-acetic acid

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About This Item

Fórmula empírica (Notação de Hill):
C11H8O5
Número CAS:
6950-82-9
Peso molecular:
220.18
Beilstein:
204777
Número MDL:
MFCD00037563
Código UNSPSC:
12352100
ID de substância PubChem:
24860338
NACRES:
NA.22

Nível de qualidade

100

Ensaio

97%

Formulário

powder

pf

212 °C (dec.) (lit.)

grupo funcional

carboxylic acid
ester

cadeia de caracteres SMILES

OC(=O)CC1=CC(=O)Oc2cc(O)ccc12

InChI

1S/C11H8O5/c12-7-1-2-8-6(3-10(13)14)4-11(15)16-9(8)5-7/h1-2,4-5,12H,3H2,(H,13,14)

chave InChI

BNHPMQBVNXMPDU-UHFFFAOYSA-N

Aplicação

7-Hydroxycoumarinyl-4-acetic acid was used in the synthesis of novel and specific enzyme substrates for Maroteaux-Lamy (MPS VI) and Morquio A (MPS IVA) diseases. It was also employed as ionic liquid matrice for MALDI-TOF MS of proteins, peptides and carbohydrates.

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H315,H319,H335

Classificações de perigo

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análise (COA)

Lot/Batch Number
0000188114
MKCD8665
MKBR2335V
MKBF6671V
MKBF6671

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7-(Diethylamino)coumarin-3-carboxylic acid BioReagent, suitable for fluorescence, ≥98.0% (HPCE)

Sigma-Aldrich

36799

7-(Diethylamino)coumarin-3-carboxylic acid

E J Demant et al.
Analytical biochemistry, 295(1), 38-44 (2001-07-31)
The fluorescence-based long-chain fatty acid probe BSA-HCA (bovine serum albumin labeled with 7-hydroxycoumarin-4-acetic acid) is shown to respond to binding of long-chain acyl-CoA thioesters by quenching of the 450 nm fluorescence emission. As determined by spectrofluorometric titration, binding affinities for
E J Demant
Analytical biochemistry, 267(2), 366-372 (1999-02-26)
A covalent complex between bovine serum albumin and 7-hydroxycoumarin-4-acetic acid (BSA-HCA) shows a strong fluorescence band at lambdamax = 450 nm upon excitation at 375 nm. Quenching of the fluorescence emission accompanies the association of fatty acids (FA) to BSA-HCA
Trisha A Duffey et al.
Bioorganic & medicinal chemistry letters, 20(20), 5994-5996 (2010-09-14)
In continued efforts to develop enzymatic assays for lysosomal storage diseases appropriate for newborn screening laboratories we have synthesized novel and specific enzyme substrates for Maroteaux-Lamy (MPS VI) and Morquio A (MPS IVA) diseases. The sulfated monosaccharide derivatives were found
Erland J F Demant et al.
The Biochemical journal, 363(Pt 3), 809-815 (2002-04-20)
The kinetics of the interaction of long-chain fatty acids (referred to as fatty acids) with albumin is critical to understanding the role of albumin in fatty acid transport. In this study we have determined the kinetics of fatty acid dissociation
Yan Chen et al.
Analytical biochemistry, 540-541, 38-44 (2017-11-13)
To establish a high throughput, low cost, and simple nanotechnology-based method for the detection of single nucleotide polymorphism (SNP) loci in type 2 diabetes mellitus (T2DM). Multiplex ligase detection reaction (LDR) amplification was performed using fluorescently labeled magnetic nanosphere-bound upstream
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