What is L-Histidine Hydrochloride Monohydrate (CAS 5934-29-2)?

L-Histidine Hydrochloride Monohydrate (CAS 5934-29-2) is a chemical compound registered under CAS number 5934-29-2. Molecular formula: C₆H₁₂ClN₃O₃. Molar mass: 209.63 g/mol. IUPAC: (2S)-2-amino-3-(1H-imidazol-5-yl)propanoic acid;hydrate;hydrochloride.

What is the CAS number of L-Histidine Hydrochloride Monohydrate (CAS 5934-29-2)?

The CAS number of L-Histidine Hydrochloride Monohydrate (CAS 5934-29-2) is 5934-29-2 — a unique Chemical Abstracts Service (CAS) identifier.

What is the molecular formula of L-Histidine Hydrochloride Monohydrate (CAS 5934-29-2)?

Molecular formula: C₆H₁₂ClN₃O₃. Molar mass: 209.63 g/mol. PSA: 93 Å².

Where can I buy L-Histidine Hydrochloride Monohydrate (CAS 5934-29-2)?

L-Histidine Hydrochloride Monohydrate (CAS 5934-29-2) is available in our shop. View the product: https://molgod.org/sds-cards/l-histidine-hydrochloride-monohydrate-cas-no-5934-29-cas-5934-29-2-xilong-scientific/

Where does the chemical data for L-Histidine Hydrochloride Monohydrate (CAS 5934-29-2) come from?

Chemical data for L-Histidine Hydrochloride Monohydrate (CAS 5934-29-2) comes from authoritative sources: PubChem (NIH). PubChem CID: 165377. Compliant with the CLP Regulation (EC 1272/2008), available under the CC-BY 4.0 licence.

L-Histidine Hydrochloride Monohydrate (CAS 5934-29-2)

Name: L-Histidine Hydrochloride Monohydrate (CAS 5934-29-2) (CAS 5934-29-2) — complete chemical dataset
Creator: MolGod
License: https://creativecommons.org/licenses/by/4.0/

Histidine Monohydrochloride Monohydrate

CAS 5934-29-2 · C₆H₁₂ClN₃O₃ · MW 209.63 g/mol

About L-Histidine Hydrochloride Monohydrate (CAS 5934-29-2)

L-Histidine Hydrochloride Monohydrate (CAS 5934-29-2) is a chemical compound registered under number CAS 5934-29-2, with the molecular formula C₆H₁₂ClN₃O₃, and a molar mass of 209.63 g/mol.

The molecule contains 25 atoms connected by 23 chemical bonds. The full systematic IUPAC name of this compound is (2S)-2-amino-3-(1H-imidazol-5-yl)propanoic acid;hydrate;hydrochloride. The interactive 3D model above lets you view the spatial arrangement of the atoms — you can rotate it with the mouse, zoom with the scroll wheel, and switch between skeletal / Ball & Stick / Space Fill visualization modes.

In terms of physicochemical properties, polar surface area PSA = 93 Å², 5 donors and 5 hydrogen bond acceptors. These parameters are key when assessing bioavailability and interaction with biomolecules.

Chemical data for this compound comes from PubChem (NIH NLM NCBI), one of the world's largest chemical databases. All information is updated automatically and enriched with GHS hazard statement translations compliant with the CLP Regulation (EC 1272/2008). The widget above may be used for educational, research and commercial purposes.

Physicochemical properties

Wzór sumaryczny	C₆H₁₂ClN₃O₃
Masa molowa	209.63 g/mol
IUPAC	(2S)-2-amino-3-(1H-imidazol-5-yl)propanoic acid;hydrate;hydrochloride
SMILES	`C1=C(NC=N1)C[C@@H](C(=O)O)N.O.Cl`
InChIKey	`CMXXUDSWGMGYLZ-XRIGFGBMSA-N`
logP (XLogP3)	—
PSA	93 Å²
HBD / HBA	5 / 5
PubChem CID	CID 165377 ↗

GHS safety

Sygnał: Uwaga

GHS07

Scientific literature

Related literature

16 artykułów · 4 open access · Źródła: PubMed, OpenAlex, Semantic Scholar

📈 Timeline publikacji (16 artykułów)

Wysokość słupka = liczba artykułów w roku. Hover dla szczegółów.

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Comparative Pharmacology of Bombesin Receptor Subtype-3, Nonpeptide Agonist MK-5046, a Universal Peptide Agonist, and Peptide Antagonist Bantag-1 for Human Bombesin Receptors

P. Moreno, S. Mantey, B. Nuche-Berenguer et al. (2013) · Journal of Pharmacology and Experimental Therapeutics

AI Summary
MK-5046 and Bantag-1 have high affinity/selectivity for hBRS-3, an orphan G-protein-coupled receptor of the bombesin (Bn) family whose natural ligand is unknown and which does not bind any natural Bn-peptide with high affinity.

Cytowania: 35Influential: 4Open AccessDOI ↗PubMed ↗PDF ↗

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Preparation, Spectrochemical, and Computational Analysis of L-Carnosine (2-[(3-Aminopropanoyl)amino]-3-(1H-imidazol-5-yl)propanoic Acid) and Its Ruthenium (II) Coordination Complexes in Aqueous Solution

Michael Lee Branham, Parvesh Singh, Krishna Bisetty et al. (2011) · Molecules

Cytowania: 35Open AccessDOI ↗PDF ↗

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Induction of anxiolytic, antidepressant and analgesic effects by Shiff base of (E)-3-(1H-imidazol-4-yl)-2-((2-oxoindolin-3-ylidene)amino)propanoic acid derivatives in diabetic rats

Mohaddese Goleij, Leila Youseftabar-Miri, Maryam Montazeri et al. (2021) · Journal of Diabetes & Metabolic Disorders

Cytowania: 15Open AccessDOI ↗PDF ↗

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SYNTHESIS, CHARACTERIZATION AND THEORETICAL CALCULATION OF 4-(((1H-IMIDAZOL-2-YL)METHYLENE)AMINO)PHENOL

Dilek ELMALI, Kader ÇITAK (2022) · Eskişehir Teknik Üniversitesi Bilim ve Teknoloji Dergisi B - Teorik Bilimler

Open AccessDOI ↗PDF ↗

In‐vitro Aluminum Determination and Preconcentration in Blood of Dialysis Patients Based on Ionic Liquid Dispersive Liquid‐Liquid Biomicroextraction by 2‐Amino‐3‐(1H‐imidazol‐4‐yl)propanoic Acid

H. Shirkhanloo, H. Z. Mousavi, M. Mohamadi (2014) · Journal of the Chinese Chemical Society

Cytowania: 1$ PaywallDOI ↗

Identification ofS-[2-carboxy-1-(1H-imidazol-4-yl)ethyl]-3-mercaptopyruvic acid with a metabolic intermediate betweenS-[2-carboxy-1-(1H-imidazol-4-yl)ethyl]-l-cysteine andS-[2-carboxy-1-(1H-imidazol-4-yl)ethyl]-3-mercaptolactic acid

M. Kinuta, H. Shimizu, N. Masuoka et al. (1997) · Amino Acids

Cytowania: 4$ PaywallDOI ↗

Chemical structure 1. Synthesis of compound 1: 3-{[2-(1H-imidazol-4-yl)ethyl]carbamoyl}propanoic acid.

$ PaywallDOI ↗

Factor XIa in complex with the inhibitor (2S)-6-amino-N-{(1S)-1-[4-(3-amino-2H-indazol-6-yl)-5-chloro-1H-imidazol-2-yl]-2-phenylethyl}-2-ethylhexanamide

A. Wei (2014)

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Propanoic Acid, 3‐((((3S)‐2‐((2S)‐2‐Amino‐3‐(4‐Hydroxy‐2,6‐Dimethylphenyl)‐1‐Oxopropyl)‐1,2,3,4‐Tetrahydro‐3‐Isoquinolinyl)Carbonyl)Amino)‐3‐(1H‐Benzimidazol‐2‐Yl)‐, (3S)‐ 1421‐14‐3

(2012) · Sax's Dangerous Properties of Industrial Materials

$ PaywallDOI ↗

Crystal structure of ((2S)-5-amino-2-((1-n-propyl-1H-imidazol-4-yl) methyl)pentanoic acid) UK396,082 a TAFIa inhibitor, Bound to Activated Porcine Pancreatic carboxypeptidaseB

D.G. Brown, R.S. Moore (2007) · Worldwide Protein Data Bank

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Structure of the DNA duplex d(AAATTT)2 with [N-(3-chloro-4-((4,5-dihydro-1H-imidazol-2-yl)amino)phenyl)-4-((4,5-dihydro-1H-imidazol-2- yl)amino)benzamide] - (drug JNI18)

C.R. Millan, C. Dardonvile, H.P. de Koning et al. (2018)

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Bovine Trypsin 2-[amino(imino)methyl]-2-hydroxyphenoxy]-6-[3-(4,5-dihydro-1H-imidazol-2-yl)phenoxy]pyridine-4-carboxylic Acid (ZK-806688) Complex

M. Whitlow (2000)

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Bovine Trypsin with 1-[2-[5-[amino(imino)methyl]-2-hydroxyphenoxy]-6-[3-(4,5-dihydro-1-methyl-1H-imidazol-2-yl)phenoxy]pyridin-4-yl]piperidine-3-carboxylic Acid (ZK-806974)

M. Whitlow (2000)

$ PaywallDOI ↗

FACTOR XIA IN COMPLEX WITH THE INHIBITOR 1-{(1S)-1-[4-(3-amino-1H-indazol-6-yl)-5-chloro-1H-imidazol-2-yl]-2-phenylethyl}-3-[5-chloro-2-(1H-tetrazol-1-yl)benzyl]urea

A. Wei (2015)

$ PaywallDOI ↗

ChemInform Abstract: Synthesis of 3‐(1‐Methyl‐1H‐imidazol‐2‐ylthio)propanoic Acid and (E)‐3‐(1‐Methyl‐1H‐imidazol‐2‐ylthio)acrylic Acid.

Christopher M. Hattan, Jalil Shojaie, Serrine S. Lau et al. (2013) · ChemInform

$ PaywallDOI ↗

Crystal structure of E.coli Phosphopantetheine Adenylyltransferase (PPAT/CoaD) in complex with 3-((1S,2S)-2-(4-hydroxy-1H-benzo[d]imidazol-2-yl)cyclopentyl)benzoic acid

M. Mamo, B.A. Appleton (2018) · Worldwide Protein Data Bank

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Dane z PubMed (NIH NLM), OpenAlex (CC0), Semantic Scholar (AI2). AI Summary wygenerowane przez Semantic Scholar TLDR. Artykuły z ikoną wymagają płatnego dostępu.

Synonyms

5934-29-2 · L-Histidine Hydrochloride Monohydrate · L-Histidine hydrochloride hydrate · L-Histidine monohydrochloride monohydrate · L-Histidine HCl hydrate · L-Histidine, monohydrochloride, monohydrate · Histidine monohydrochloride monohydrate · Histidine hydrochloride hydrate · Histidine, monohydrochloride, monohydrate, L- · X573657P6P · histidine hydrochloride monohydrate · L-Histidine hydrochloride hydrate (JP17) · L-HISTIDINE HYDROCHLORIDE HYDRATE [JAN] · HISTIDINE, L-, HYDROCHLORIDE MONOHYDRATE · HISTIDINE, L-, MONOHYDROCHLORIDE MONOHYDRATE

Data sources

📊 PubChem CID 165377 — NIH
🔬 NIST WebBook — spektroskopia
🌐 Wikidata
💊 ChEMBL — bioaktywność

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