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H7750

Sigma-Aldrich

DL-Histidine

≥99% (TLC), suitable for ligand binding assays

Synonyme(s) :

(±)-2-Amino-3-(4-imidazolyl)propionic acid

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About This Item

Formule empirique (notation de Hill):
C6H9N3O2
Numéro CAS:
4998-57-6
Poids moléculaire :
155.15
Numéro Beilstein :
7800
Numéro CE :
225-660-9
Numéro MDL:
MFCD00005208
Code UNSPSC :
12352209
eCl@ss :
32160406
ID de substance PubChem :
24895803
Nomenclature NACRES :
NA.26

product name

DL-Histidine, ≥99% (TLC)

Niveau de qualité

200

Pureté

≥99% (TLC)

Forme

powder

Technique(s)

ligand binding assay: suitable

Pf

273 °C (dec.) (lit.)

Solubilité

0.5 M HCl: soluble

Application(s)

peptide synthesis

Chaîne SMILES 

NC(Cc1c[nH]cn1)C(O)=O

InChI

1S/C6H9N3O2/c7-5(6(10)11)1-4-2-8-3-9-4/h2-3,5H,1,7H2,(H,8,9)(H,10,11)

Clé InChI

HNDVDQJCIGZPNO-UHFFFAOYSA-N

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Catégories apparentées

Application

DL-Histidine has been used to study the fouling behaviour of polyethersulfone ultrafiltration membranes made with different PVP (polyvinylpyrrolidone).
DL-Histidine is the mixed isomer of D- and L-histidine. DL-Histidine may be used to evaluate the efficiency of amino acid chiral ligand exchange media and systems and in running buffers for capillary electrophoresis.

Actions biochimiques/physiologiques

L-Histidine is involved in the one-carbon unit metabolism. It is associated with protein methylation. L-Histidine is a part of hemoglobin structure and function. L-Histidine is a component of dipeptides with antioxidative property. Histidine serves as a precursor for the formation of histamine, which is associated with allergic responses. Urocanic acid, an immune response modulator in skin is also biosynthesised from histidine.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)

Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Fouling behaviour of polyethersulfone UF membranes made with different PVP
J.Marchese
Journal of Membrane Science , 211, 1-11 (2009)
Worapan Pormsila et al.
Electrophoresis, 32(8), 884-889 (2011-03-12)
The quantification of plasma lactate and evaluation of the lactate threshold by CE with capacitively coupled contactless conductivity is demonstrated. The only sample preparation needed was deproteinization with a ACN/methanol mixture. A solution of 10 mmol/L 2-morpholinoethanesulfonic acid monohydrate, 10
Yoshikazu Tsukasaki et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(45), 16011-16016 (2014-10-31)
The cadherins Fat and Dachsous regulate cell polarity and proliferation via their heterophilic interactions at intercellular junctions. Their ectodomains are unusually large because of repetitive extracellular cadherin (EC) domains, which raises the question of how they fit in regular intercellular
Tetsuya Chujo et al.
PloS one, 9(6), e98737-e98737 (2014-06-04)
WRKY transcription factors and mitogen-activated protein kinase (MAPK) cascades have been shown to play pivotal roles in the regulation of plant defense responses. We previously reported that OsWRKY53-overexpressing rice plants showed enhanced resistance to the rice blast fungus. In this
Ana E Zeraik et al.
International journal for parasitology, 44(8), 523-531 (2014-04-29)
Septins are guanosine-5'-triphosphate-binding proteins involved in wide-ranging cellular processes including cytokinesis, vesicle trafficking, membrane remodelling and scaffolds, and with diverse binding partners. Precise roles for these structural proteins in most processes often remain elusive. Identification of small molecules that inhibit
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