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D8388

Sigma-Aldrich

Dimethyl pimelimidate dihydrochloride

powder

Sinônimo(s):

DMP, Dimethyl pimelinediimidate dihydrochloride

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About This Item

Fórmula linear:
[CH3OC(=NH)CH2CH2]2CH2 · 2HCl
Número CAS:
58537-94-3
Peso molecular:
259.17
Número CE:
261-320-6
Número MDL:
MFCD00038942
Código UNSPSC:
12171500
ID de substância PubChem:
24894208
NACRES:
NA.25

Formulário

powder

Nível de qualidade

200

adequação da reação

reagent type: cross-linking reagent

solubilidade

H2O: 10 mg/mL

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

Cl.Cl.COC(=N)CCCCCC(=N)OC

InChI

1S/C9H18N2O2.2ClH/c1-12-8(10)6-4-3-5-7-9(11)13-2;;/h10-11H,3-7H2,1-2H3;2*1H

chave InChI

LRHXBHUTQWIZTN-UHFFFAOYSA-N

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Descrição geral

Dimethyl pimelimidate dihydrochloride is a homobifunctional cross-linking reagent used in crosslinking, protein interaction and protein modification. It typically reacts with primary amines in the pH range 7.0-10.0 to form amidine bonds.

Aplicação

Dimethyl pimelimidate dihydrochloride has been used to develop a technique for isolating Enterocytozoon bieneusi spores directly from human stool samples with a high degree of purity, which opens up new approaches for studying this parasite.

Atenção

The reagent is readily hydrolyzed at neutral pH.

Outras notas

2024 CiteAb Award Winner for Supplier Succeeding in Parkinson′s Research
Note that the amidine linkage preserves original primary amine positive charge. Incorporates a seven atom linker.

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H315

Classificações de perigo

Skin Irrit. 2

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
BCCF0376
BCBL2157V
1418431V
1418431
1324459

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K Brew et al.
The Journal of biological chemistry, 250(4), 1434-1444 (1975-02-25)
The cross-linking of the two components of lactose synthetase, alpha-lactalbumin and a galactosyltransferase, with dimethylpimelimidate was examined. The extent of the cross-linking at pH 8.1 was found to be dependent upon the presence of substrates or inhibitors for the galactosyltransferase.
G B Karlsson et al.
Analytical biochemistry, 199(2), 219-222 (1991-12-01)
A method is described for the use of magnetic beads as a solid phase for the immunoprecipitation of labeled proteins. The anti-human transferrin receptor monoclonal antibody OKT-9 has been coupled to sheep anti-mouse IgG1-coated magnetic beads using the crosslinking agent
I Accoceberry et al.
Journal of clinical microbiology, 39(5), 1947-1951 (2001-04-28)
An original, reliable, and reproducible method for the purification of Enterocytozoon bieneusi spores from human stools is described. We recently reported the production of a species-specific monoclonal antibody (MAb) 6E52D9 immunoglobulin G2a (IgG2a) raised against the exospore of E. bieneusi
Semisynthetic fluorohydrolases prepared by chemical modification of ribonuclease.
David, E., et al.
Enz. Microbiol. Technol., 14, 885-892 (1992)
Kevin Michael Boehm et al.
BMC bioinformatics, 20(1), 7-7 (2019-01-07)
To further our understanding of immunopeptidomics, improved tools are needed to identify peptides presented by major histocompatibility complex class I (MHC-I). Many existing tools are limited by their reliance upon chemical affinity data, which is less biologically relevant than sampling
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