Chloramphenicol - Moligand™, 10mM in DMSO , CAS No.56-75-7

CAS: 56-75-7 Cat. No.: C408156 Formule: C11H12Cl2N2O5 Poids moléculaire: 323.13 Beilstein Registry Number: 2225532 Numéro CE: 200-287-4
DISPONIBLE À COMMANDE
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. 10mM in DMSO
Synonyms
Chloromycetin | 2,​2-​dichloro-​N-​[(1R,​2R)​-​2-​hydroxy-​1-​(hydroxymethyl)​-​2-​(4-​nitrophenyl)​ethyl]​-acetamide
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Size
USA
Allemagne (EU)*
Price
Qty
1ml
C408156-1ml
4 En stock
—
19,90$US
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Why this grade

Moligand™, 10mM in DMSO Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

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Quality documents

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

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Literature proof

Cited in 328 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Vue d’ensemble

Information

Chloramphenicol Chloramphenicol (Chloromycetin) is a bacteriostatic by inhibiting protein synthesis.
In vitro

Chloramphenicol results in a constitutive increase in the level of cspA transcript and constitutive production of CS7.4. Chloramphenicol down-regulates the mitochondrial DNA-encoded Cox I protein, but not nuclear-encoded proteins. Chloramphenicol increases cellular levels of the p21(waf1/cip1) protein and p21(waf1/cip1) mRNA through a p53-independent pathway. Chloramphenicol, at concentrations greater than 0.1 g/L (0.3 mM), inhibits the denitrifying enzyme activity (DEA) of slurries of humisol and sandy loam soils by disrupting the activity of existing nitrate reductase enzymes. Chloramphenicol, at concentrations from 5 mM to 2 mM initiates apoptosis in dividing cells from a monkey kidney-derived cell line and in haematopoietic progenitor cells from human neonatal cord blood. Chloramphenicol suppresses growth of progenitor cells.

In vivo

Chloramphenicol results in increased t1/2(beta) (by 209%), and decreased ClB (by 45%), and prolonged recovery indices (by 768 to 946%) in greyhounds. Chloramphenicol suppresses increases in the body weight and liver weight of experimental animals and at the same time induced a remarkable increase in lipid peroxidation in the liver during the formation of megamitochondria. Chloramphenicol-induced formation of megamitochondria is not simply ascribed to the suppression of the dividing process of mitochondria due to lowered protein synthesis in mitochondria but is intimately related to oxidative stress.
Cell Data

cell lines:MCF-7 cells

Concentrations:

Incubation Time:

Powder Purity:≥99%

Specifications

Synonymes
Chloromycetin | 2,​2-​dichloro-​N-​[(1R,​2R)​-​2-​hydroxy-​1-​(hydroxymethyl)​-​2-​(4-​nitrophenyl)​ethyl]​-acetamide
Spécifications et pureté
Moligand™, 10mM in DMSO
Mécanismes biochimiques et physiologiques
Chloramphenicol (Chloromycetin) is a bacteriostatic by inhibiting protein synthesis.
Conditions de stockage de stockage
Store at -80°C
Expédié en
Dry ice packs + Cold packs
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Grade
Moligand™
Propriétés du produit
ALogP
1.1
Noms et identifiants
Isomères SMILES
C1=CC(=CC=C1[C@H]([C@@H](CO)NC(=O)C(Cl)Cl)O)[N+](=O)[O-]
WGK Allemagne
3
RTECS
AB6825000
Poids moléculaire
323.13
Beilstein
2225532
Reaxy-Rn
2063328
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2063328&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

Cibles associées (humaines)
TAS2R41 Tchem Taste receptor type 2 member 41 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
TAS2R8 Tchem Taste receptor type 2 member 8 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propriétés chimiques et physiques
SolubilitéSolubility (25°C) In vitro DMSO: 5 mg/mL warmed with 50ºC Water: bath (6.68 mM); Water: Insoluble; Ethanol: Insoluble;
Rotation spécifique [α]20 ° (C=5, EtOH)
Point d'éclair (°F)57.2°F closed cup
Point d'éclair (°C)14.0°C closed cup
Point de fusion (°C)149-153°C
FAQ et articles
Five Key Structural Features of Plasmids
How Antibiotics Halt Bacterial Protein Synthesis (With Representative Products and a Selection Guide)
A Practical Guide to Selecting and Using Common Antibiotics in Research
16 Frequently Asked Questions About Nourseothricin
Azithromycin: Physicochemical Features, Mechanism of Action, and Key Points for Research Applications
Comparison of Chloramphenicol and Common Antibiotic Resistance Selection Systems in Molecular Cloning
What Is Synthetic Biology? The Industrialization Pathway from Upstream Reagent Toolchains to Biomanufacturing Applications
Citations of This Product
Calculateurs de solution
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