DL-Histidina - ≥98% , CAS No.4998-57-6

CAS: 4998-57-6 Cat. No.: H111055 Peso molecular: 155.15 Beilstein Registry Number: 7800 Número EC: 225-660-9
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
UNII-QU6SDF3Q03 | (+/-)-HISTIDINE | 1H-IMIDAZOLE-4-ALANINE | NSC_773 | 1H-Imidazole-4-propanoic acid, (S)- | 2-Amino-3-(4-imidazolyl)propionic acid | DL-HISTIDINE | Histidine # | A812881 | Histidine, DL- | FT-0627842 | AKOS000269100 | SR-01000596947-1 | C
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
H111055-1g
5
9,90US$
5g
H111055-5g
3
25,90US$
25g
H111055-25g
4
63,90US$
100g
H111055-100g
2
224,90US$
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Aplicación:

La DL-Histidina se ha utilizado para estudiar el comportamiento de ensuciamiento de las membranas de ultrafiltración de polietersulfona fabricadas con diferentes PVP (polivinilpirrolidona).

La DL-histidina es el isómero mixto de la D- y la L-histidina. La DL-histidina puede utilizarse para evaluar la eficacia de los medios y sistemas de intercambio de ligandos quirales de aminoácidos y en tampones de funcionamiento para electroforesis capilar.


Specifications

Sinónimos
UNII-QU6SDF3Q03 | (+/-)-HISTIDINE | 1H-IMIDAZOLE-4-ALANINE | NSC_773 | 1H-Imidazole-4-propanoic acid, (S)- | 2-Amino-3-(4-imidazolyl)propionic acid | DL-HISTIDINE | Histidine # | A812881 | Histidine, DL- | FT-0627842 | AKOS000269100 | SR-01000596947-1 | C
Especificaciones y pureza
≥98%
Mecanismos bioquímicos y fisiológicos
La L-histidina interviene en el metabolismo de las unidades de un carbono. Está asociada a la metilación de proteínas. La L-histidina forma parte de la estructura y función de la hemoglobina. La L-histidina es un componente de dipéptidos con propiedades a
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488179550
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488179550
Sonrisas canónicasC1=C(NC=N1)CC(C(=O)O)N
IUPAC Name2-amino-3-(1H-imidazol-5-yl)propanoic acid
InChIKeyHNDVDQJCIGZPNO-UHFFFAOYSA-N
INCHI1S/C6H9N3O2/c7-5(6(10)11)1-4-2-8-3-9-4/h2-3,5H,1,7H2,(H,8,9)(H,10,11)
Isómeros SMILES C1=C(NC=N1)CC(C(=O)O)N
WGK Alemania 3
Peso molecular 155.15
Beilstein 7800
Reaxy-Rn 7800
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=7800&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClaseCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives
Direct ParentHistidine and derivatives
Alternative Parents Alpha amino acids  Imidazolyl carboxylic acids and derivatives  Aralkylamines  Heteroaromatic compounds  Amino acids  Monocarboxylic acids and derivatives  Carboxylic acids  Azacyclic compounds  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Histidine or derivatives - Alpha-amino acid - Imidazolyl carboxylic acid derivative - Aralkylamine - Azole - Imidazole - Heteroaromatic compound - Amino acid - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Carboxylic acid - Organic nitrogen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Organic oxide - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Amine - Hydrocarbon derivative - Aromatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as histidine and derivatives. These are compounds containing cysteine or a derivative thereof resulting from reaction of cysteine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
External Descriptors imidazoles - alpha-amino acid
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

15 results found

Lot NumberCertificate TypeFechaArticulo
C2222079Certificate of AnalysisJan 19, 2026 H111055
J2126226Certificate of AnalysisAug 11, 2025 H111055
J2009164Certificate of AnalysisJul 03, 2024 H111055
H1521028Certificate of AnalysisJun 05, 2023 H111055
B2303649Certificate of AnalysisDec 09, 2022 H111055
B2303662Certificate of AnalysisDec 09, 2022 H111055
B2303665Certificate of AnalysisDec 09, 2022 H111055
B2303670Certificate of AnalysisDec 09, 2022 H111055
B2303671Certificate of AnalysisDec 09, 2022 H111055
B2303676Certificate of AnalysisDec 09, 2022 H111055
B2303678Certificate of AnalysisDec 09, 2022 H111055
B2303682Certificate of AnalysisDec 09, 2022 H111055
C2617071Certificate of AnalysisDec 09, 2022 H111055
C2222078Certificate of AnalysisFeb 14, 2022 H111055
D2415432Certificate of AnalysisFeb 14, 2022 H111055

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Propiedades químicas y físicas
Solubilidad0.5 M HCl: soluble
Punto de fusión (°C)273°C
Peso molecular155.150 g/mol
XLogP3-3.200
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count4
Rotatable Bond Count3
Exact Mass155.069 Da
Monoisotopic Mass155.069 Da
Topological Polar Surface Area92.000 Ų
Heavy Atom Count11
Formal Charge0
Complexity151.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Jian Zhang, Lingling Liang, Yanqing Miao, Yang Yang, Xin Bao, Chunye Liu.  (2022)  Open-tubular capillary electrochromatography with hydroxypropyl-β-cyclodextrin imprinted polymers: hybrid polyhedral oligomeric silsesquioxane as a coating for enantioseparation.  RSC Advances,  12  (16): (9637-9644).  [PMID:35424918] [10.1039/D2RA00079B]
2. Qing Xiong, Jing Jin, Liqiong Lv, Zhisi Bu, Shengqiang Tong.  (2018)  Chiral ligand exchange countercurrent chromatography: Enantioseparation of amino acids.  JOURNAL OF SEPARATION SCIENCE,  41  (6): (1479-1488).  [PMID:29323783] [10.1002/jssc.201701117]
3. Quanzhou Xu, Xing Fei, Xueqing Qiu, Xiaofei Wang, Tiejun Wang, Xuliang Lin, Sha Li, Yanlin Qin.  (2024)  Structure regulation of lignin-derived N-doped carbon-supported Ni catalyst for efficient upgrading of ethanol to higher alcohols.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2024.151092]
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