Erythromycin CAS#114-07-08

Erythromycin CAS#114-07-08

Erythromycin (CAS No.: 114-07-8) - Macrolide Antibacterial For Gram-Positive & Atypical Infections As a professional supplier of pharmaceutical-grade and veterinary-grade antibacterial active ingredients, we provide high-purity Erythromycin that strictly complies with global pharmacopoeia standards (USP, EP, BP, CP). A natural macrolide antibiotic derived from Streptomyces erythreus, it exhibits potent bacteriostatic (and bactericidal at high doses) activity against Gram-positive bacteria and atypical pathogens. It is widely used in human medicine for treating respiratory, skin, and soft tissue infections—especially in patients allergic to penicillins—and in veterinary practice for livestock and companion animals, serving as a foundational agent in antibacterial therapy.
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Description

Erythromycin (CAS No.: 114-07-8) - Macrolide Antibacterial for Gram-Positive & Atypical Infections

As a professional supplier of pharmaceutical-grade and veterinary-grade antibacterial active ingredients, we provide high-purity Erythromycin that strictly complies with global pharmacopoeia standards (USP, EP, BP, CP). A natural macrolide antibiotic derived from Streptomyces erythreus, it exhibits potent bacteriostatic (and bactericidal at high doses) activity against Gram-positive bacteria and atypical pathogens. It is widely used in human medicine for treating respiratory, skin, and soft tissue infections-especially in patients allergic to penicillins-and in veterinary practice for livestock and companion animals, serving as a foundational agent in antibacterial therapy.

Product Basic Information

Item Details
Product Name Erythromycin
CAS No. 114-07-8 (Note: Correct CAS for Erythromycin; the "114-07-08" provided is a typo)
Synonyms (3R,4S,5S,6R,7R,9R,10R,11R,12S,13R)-6,11,12,13-Tetrahydroxy-3,7,9,11,13-pentamethyl-10-[(E)-1-oxo-3-(3,4,5-trihydroxyphenyl)prop-2-en-1-yl]-2,4,6,8,10,12-hexahydro-1H-3,5,7-trioxacyclopentadecine-1,9-dione
Molecular Formula C₃₇H₆₇NO₁₃
Molecular Weight 733.93
Appearance White to off-white crystalline powder or hygroscopic granules; Odorless or with a slight characteristic odor
Specification - Pharmaceutical Grade: Purity ≥98.0% (HPLC); Assay 950–1050 μg/mg (anhydrous basis); Loss on drying ≤2.0%; Heavy metals (Pb≤5ppm, Hg≤1ppm, Cd≤1ppm); Residual solvents (ethanol ≤500ppm, acetone ≤500ppm)- Veterinary Grade: Purity ≥95.0% (HPLC); Assay 900–1100 μg/mg; Heavy metals ≤10ppm
Melting Point 135–140°C (with decomposition)
Solubility Practically insoluble in water (≈0.1 g/L at 25°C); Soluble in ethanol (≈50 g/L), methanol (≈80 g/L), chloroform (≈200 g/L), and acetone; Slightly soluble in ether
Storage Conditions Store in a cool (15–25°C), dry, light-protected container; Sealed to prevent moisture absorption (hygroscopic) and degradation (sensitive to acid/alkali); Avoid contact with strong oxidizing agents; Shelf life: 36 months for pharmaceutical grade, 24 months for veterinary grade

Core Functions & Mechanism of Action

Erythromycin exerts its antibacterial effect by targeting the bacterial ribosome, inhibiting protein synthesis-critical for bacterial growth and survival:

Ribosome Binding:is binds reversibly to the 50S subunit of the bacterial ribosome, specifically interacting with the 23S rRNA and ribosomal proteins L4 and L22.

Protein Synthesis Blockade: This binding prevents the translocation step of protein synthesis-blocking the movement of the ribosome along mRNA and halting the addition of new amino acids to the growing peptide chain.

Bacteriostatic/Bactericidal Activity: At standard doses, it suppresses bacterial growth (bacteriostatic); at high doses or against susceptible strains (e.g., Streptococcus pneumoniae), it can kill bacteria (bactericidal) by disrupting membrane integrity.

Key antibacterial spectrum advantages:

Gram-Positive Coverage: Active against Staphylococcus aureus (MSSA), Streptococcus pyogenes (Group A strep), Streptococcus pneumoniae, and Corynebacterium diphtheriae-ideal for penicillin-allergic patients.

Atypical Pathogen Coverage: Effective against Mycoplasma pneumoniae, Chlamydophila pneumoniae, Chlamydia trachomatis, and Legionella pneumophila-critical for respiratory and sexually transmitted infections (STIs).

Gram-Negative Coverage: Inhibits select Gram-negative bacteria like Haemophilus influenzae and Neisseria gonorrhoeae (though not first-line for these pathogens).

Core Applications

Erythromycin CAS#114-07-08 is administered orally (tablets, capsules, suspensions) or topically (ointments, eye drops); parenteral formulations (IV) are also available for severe infections. It is not active against viral infections (e.g., cold/flu) or Gram-negative rods (e.g., E. coli, Klebsiella).

1. Human Pharmaceutical Field

1.1 Respiratory Tract Infections

Community-Acquired Pneumonia (CAP): Treats CAP caused by Mycoplasma pneumoniae, Chlamydophila pneumoniae, or penicillin-sensitive S. pneumoniae (penicillin-allergic patients). Oral dose: 500 mg every 6 hours or 1 g every 12 hours for 7–14 days; IV dose: 500 mg–1 g every 6 hours for severe cases.

Acute Pharyngitis/Tonsillitis: For Streptococcus pyogenes infections (penicillin-allergic patients). Oral dose: 250 mg every 6 hours for 10 days (prevents rheumatic fever).

Legionnaires' Disease: First-line therapy for Legionella pneumophila infections. IV/oral dose: 1–2 g daily (divided into 4 doses) for 10–14 days.

1.2 Skin & Soft Tissue Infections

Impetigo & Cellulitis: Treats Staphylococcus aureus or Streptococcus pyogenes infections. Oral dose: 250–500 mg every 6 hours for 7–10 days; topical ointment (2%) applied 3–4 times daily for mild cases.

Diphtheria: Adjuvant therapy to diphtheria antitoxin, eliminating Corynebacterium diphtheriae from the throat. Oral dose: 250–500 mg every 6 hours for 14 days.

1.3 Sexually Transmitted Infections (STIs)

Chlamydia Trachomatis Infections: Treats urethritis, cervicitis, or pelvic inflammatory disease (PID) in patients allergic to azithromycin. Oral dose: 500 mg twice daily for 7 days.

Gonorrhea: Alternative therapy for Neisseria gonorrhoeae (when first-line agents are unavailable). Oral dose: 500 mg every 6 hours for 7 days (combined with probenecid for enhanced efficacy).

1.4 Topical Infections

Ophthalmic Infections: Eye ointment (0.5%) for bacterial conjunctivitis (e.g., Haemophilus influenzae, Staphylococcus aureus)-applied 1–2 times daily for 7–10 days.

Acne Vulgaris: Topical gel/ointment (2%) for mild-to-moderate acne, reducing Cutibacterium acnes colonization-applied once daily.

2. Veterinary Field (Livestock & Companion Animals)

CAS#114-07-08 is used to treat bacterial infections in cattle, pigs, chickens, dogs, and cats:

Bovine Respiratory Disease (BRD): Caused by Mannheimia haemolytica or Mycoplasma bovis. IM/oral dose: 10–20 mg/kg body weight once daily for 3–5 days.

Porcine Respiratory Disease Complex (PRDC): For Mycoplasma hyopneumoniae or Streptococcus suis infections. Oral dose: 20–40 mg/kg feed for 7–10 days.

Poultry Chronic Respiratory Disease (CRD): Treats Mycoplasma gallisepticum infections in chickens. Oral dose: 10–20 mg/kg drinking water for 5–7 days.

Canine/Feline Skin & Ear Infections: For Staphylococcus pseudintermedius (skin) or Mycoplasma spp. (ears). Oral dose: 10–20 mg/kg twice daily for 7–14 days; topical ear drops (0.5%) applied twice daily.

Contraindications: Avoid use in horses (colitis risk) or animals with pre-existing hepatic impairment; not approved for dairy cattle producing milk for human consumption.

Quality & Safety Assurance

As a widely used macrolide antibiotic, Erythromycin CAS#114-07-08 requires strict quality control to ensure potency, purity, and safety-especially given its potential for gastrointestinal side effects and drug interactions:

1. Manufacturing & Purity Control

Production: Produced via microbial fermentation of Streptomyces erythreus, followed by purification (solvent extraction, chromatography) and crystallization. The process ensures:

Minimal impurities (e.g., degradation products, related macrolides) ≤1.0% (pharmaceutical grade);

Consistent potency (950–1050 μg/mg) for reliable therapeutic effect.

GMP Compliance: Pharmaceutical-grade Erythromycin CAS#114-07-08 is manufactured in Grade D cleanrooms (per ICH Q7 guidelines); veterinary grade complies with GMP for animal pharmaceuticals.

2. Comprehensive Testing Protocol

Test Item Method Acceptance Criterion
Purity & Assay HPLC (C18 column, 210 nm detection) Pharmaceutical grade: ≥98.0% purity; Assay 950–1050 μg/mg
Related Substances HPLC (gradient elution) Single impurity ≤0.5%; Total impurities ≤1.0% (pharmaceutical grade)
Heavy Metals ICP-MS (Inductively Coupled Plasma-Mass Spectrometry) Pharmaceutical grade: Pb≤5ppm; Veterinary grade: ≤10ppm
Residual Solvents GC (headspace sampling, FID detector) Class 2 solvents ≤500ppm; Class 1 solvents not detected
Loss on Drying Gravimetric method (105°C for 2 hours) ≤2.0% (pharmaceutical grade)
Identification IR Spectroscopy & HPLC Retention Time Matches reference standard spectrum; Retention time consistent with standard

3. Safety Reminders

Human Use:

Contraindications: Hypersensitivity to macrolide antibiotics; history of QT interval prolongation (avoid with antiarrhythmic drugs like amiodarone); severe hepatic impairment.

Adverse Effects: Common: gastrointestinal upset (nausea, diarrhea, abdominal pain) (mitigated with enteric-coated formulations); rare but serious: cholestatic jaundice (reversible upon discontinuation), ototoxicity (high doses).

Drug Interactions: Inhibits CYP3A4 enzymes-avoid concurrent use with warfarin (increased bleeding risk), simvastatin (rhabdomyolysis risk), or cyclosporine (increased nephrotoxicity risk).

Veterinary Use:

Withdrawal Periods: Cattle: 21 days (meat); Pigs: 14 days (meat); Chickens: 7 days (meat/eggs); Dogs/Cats: No withdrawal period (non-food animals).

Residue Warning: Prohibited in dairy cattle (milk residues) and laying hens (egg residues) beyond the withdrawal period.

Cooperation & Contact

We supply Erythromycin in grades and forms tailored to human and veterinary applications:

Pharmaceutical Grade: Fine powder or enteric-coated granules (1kg–100kg per order, sealed aluminum foil bags with desiccants) for oral/topical formulations.

Veterinary Grade: Powder for livestock oral premixes or injectables (10kg–500kg per order; monthly production capacity of 2500kg).

Value-added services include:

Providing DMF (Drug Master File) and CEP (Certificate of Suitability) for pharmaceutical-grade products to support EU/US/Asia registration.

Technical support for enteric coating (reducing gastrointestinal side effects) and veterinary formulation stability testing.

Batch-specific COA with purity, assay, and residual solvent results to ensure regulatory compliance.

If you are a pharmaceutical manufacturer, nutraceutical brand, or veterinary drug enterprise, please contact us for detailed cooperation:

Contact Information:

Email: sales@huarongpharma.com

Phone/WhatsApp: +86 13751168070

We adhere to the principles of "antibacterial efficacy, safety compliance, and versatility" and look forward to partnering with global healthcare and animal health industries!

 

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