Tetracycline hydrochloride structure
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Common Name | Tetracycline hydrochloride | ||
|---|---|---|---|---|
| CAS Number | 64-75-5 | Molecular Weight | 480.896 | |
| Density | N/A | Boiling Point | 799.4ºC at 760 mmHg | |
| Molecular Formula | C22H25ClN2O8 | Melting Point | 220-223 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 437.3ºC | |
| Symbol |
GHS07 |
Signal Word | Warning | |
Use of Tetracycline hydrochlorideTetracycline hydrochloride is a broad-spectrum antibiotic used to treat a wide range of infections. |
This table lists Chinese names, IUPAC names and various aliases of this chemical substance.
| Name | Tetracycline hydrochloride |
|---|---|
| Synonym | More Synonyms |
This table contains bioactivity, target information and biological‑assay experimental data of this compound.
| Description | Tetracycline hydrochloride is a broad-spectrum antibiotic used to treat a wide range of infections. |
|---|---|
| Related Catalog | |
| In Vitro | Tetracyclines are broad-spectrum agents, exhibiting activity against a wide range of gram-positive and gram-negative bacteria, atypical organisms such as chlamydiae, mycoplasmas, and rickettsiae, and protozoan parasites. Tetracyclines inhibit bacterial protein synthesis by preventing the association of aminoacyl-tRNA with the bacterial ribosome. Tetracyclines traverse the outer membrane of gram-negative enteric bacteria through the OmpF and OmpC porin channels, as positively charged cation (probably magnesium)-tetracycline coordination complexes [1]. |
| In Vivo | The tetracyclines have applications for the treatment of infections in poultry, cattle, sheep, and swine. In some cases, e.g., for therapeutic treatment of large numbers of poultry reared on commercial farms, the antibiotics are added directly to feed or water or can be administered in aerosols. Tetracyclines could be used as growth promotion or growth enhancement. Tetracyclines are used in aquaculture to control infections in salmon, catfish, and lobsters[2]. |
| References |
This table shows physicochemical parameters including melting point, boiling point, density, solubility and optical rotation. Missing data is marked as N/A.
| Boiling Point | 799.4ºC at 760 mmHg |
|---|---|
| Melting Point | 220-223 °C(lit.) |
| Molecular Formula | C22H25ClN2O8 |
| Molecular Weight | 480.896 |
| Flash Point | 437.3ºC |
| Exact Mass | 480.129944 |
| PSA | 181.62000 |
| LogP | 1.28790 |
| Vapour Pressure | 5.82E-27mmHg at 25°C |
| Index of Refraction | -253 ° (C=0.5, 0.1mol/L HCl) |
| InChIKey | YCIHPQHVWDULOY-FMZCEJRJSA-N |
| SMILES | CN(C)C1C(=O)C(C(N)=O)=C(O)C2(O)C(=O)C3=C(O)c4c(O)cccc4C(C)(O)C3CC12.Cl |
| Water Solubility | 50 g/L |
This table provides MSDS information including hazard classification, first‑aid, fire‑fighting, spill handling, operation and storage instructions.
This table summarizes toxicological test data, acute & chronic toxicity and ecological hazard parameters for this chemical.
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
MUTATION DATA
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This table covers safety warnings, protective measures, incompatible substances and disposal guidelines for this compound.
| Symbol |
GHS07 |
|---|---|
| Signal Word | Warning |
| Hazard Statements | H315-H319-H335 |
| Precautionary Statements | P305 + P351 + P338 |
| Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
| Hazard Codes | Xi:Irritant |
| Risk Phrases | R36/37/38 |
| Safety Phrases | S26-S36 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 2 |
| RTECS | QI9100000 |
| HS Code | 29413000 |
This table presents publicly reported synthetic routes, reaction conditions, reactants and product information of the compound.
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Tetracycline hy... CAS#:64-75-5 |
| Literature: WO2005/112945 A2, ; Page/Page column 106-107 ; |
This table lists upstream starting materials and downstream derivative products related to this chemical.
| Precursor 1 | |
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| DownStream 1 | |
This table shows customs‑related data including HS‑code, tariff and regulatory conditions for import and export.
| HS Code | 29413000 |
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This table lists relevant public references with title, journal and publication metadata for this compound.
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Selective growth-inhibitory effect of 8-hydroxyquinoline towards Clostridium difficile and Bifidobacterium longum subsp. longum in co-culture analysed by flow cytometry.
J. Med. Microbiol. 63(Pt 12) , 1663-9, (2014) The major risk factor for Clostridium difficile infection (CDI) is the use of antibiotics owing to the disruption of the equilibrium of the host gut microbiota. To preserve the beneficial resident pro... |
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Pre-microRNA binding aminoglycosides and antitumor drugs as inhibitors of Dicer catalyzed microRNA processing.
Bioorg. Med. Chem. Lett. 22 , 1709-11, (2012) Over-expressions of miRNAs are being increasingly linked with many diseases including different types of cancer. In this study, the role of some known small molecular therapeutics has been investigate... |
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Development of a Method for the Analysis of Multiclass Antibiotic Residues in Milk Using QuEChERS and Liquid Chromatography-Tandem Mass Spectrometry.
Foodborne Pathog. Dis. 12 , 693-703, (2015) A precise and simplified method of sample preparation for the simultaneous quantification of the antibiotics β-lactam, macrolide, tetracycline, sulfonamide, and quinolone in bovine milk was developed.... |
This table contains target information, in‑vitro & in‑vivo assay data for this compound.
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Name: Antimicrobial activity against Bifidobacterium thermophilum ATCC 25866
Source: ChEMBL
Target: Bifidobacterium thermophilum
External Id: CHEMBL910836
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Name: Antimicrobial activity against Bifidobacterium breve R0070
Source: ChEMBL
Target: Bifidobacterium breve
External Id: CHEMBL910837
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Name: Antimicrobial activity against 60 min 1 M HCl-stressed Bifidobacterium animalis ATCC ...
Source: ChEMBL
Target: NON-PROTEIN TARGET
External Id: CHEMBL910838
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Name: Primary qHTS assay for inhibitors of alpha-synuclein gene (SNCA) expression
Source: NCGC
External Id: SNCA-p-activity-luciferase
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Name: Antimicrobial activity against 60 min 1 M HCl-stressed Bifidobacterium bifidum R0071 ...
Source: ChEMBL
Target: Bifidobacterium bifidum
External Id: CHEMBL910839
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Name: Antimicrobial activity against Bifidobacterium longum ATCC 15708
Source: ChEMBL
Target: Bifidobacterium longum
External Id: CHEMBL910832
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Name: Antimicrobial activity against Bifidobacterium longum R0175
Source: ChEMBL
Target: Bifidobacterium longum
External Id: CHEMBL910833
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Name: Cytochrome P450 Family 1 Subfamily A Member 2 (CYP1A2) small molecule antagonists: lu...
Source: 824
External Id: CYP273
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Name: Antimicrobial activity against Bifidobacterium longum P/N 601377
Source: ChEMBL
Target: Bifidobacterium longum
External Id: CHEMBL910834
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Name: Antimicrobial activity against Bifidobacterium pseudolongum ATCC 25562
Source: ChEMBL
Target: NON-PROTEIN TARGET
External Id: CHEMBL910835
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This table collects all English aliases, systematic names and CAS‑related synonyms of the compound.
| achromycin hydrochloride |
| paltet |
| u-5965 |
| EINECS 200-593-8 |
| alatet |
| partrex |
| Tetracycline (hydrochloride) |
| tetracycline HCl |
| teline |
| MFCD00078142 |
| sumycin |
| tet-cy |
| quatrex |
| qidtet |
| unicin |
This section contains frequently‑asked‑questions about this compound, including basic parameters, properties, storage conditions and corresponding answers.
| Q: What are the downstream products of Tetracycline hydrochloride? |
| A: Related downstream products(CAS) of Tetracycline hydrochloride: 60-54-8. |
| Q: What English synonyms does Tetracycline hydrochloride have? |
| A: English synonyms of Tetracycline hydrochloride: achromycin hydrochloride, paltet, u-5965, EINECS 200-593-8, alatet, partrex, Tetracycline (hydrochloride), tetracycline HCl, teline, MFCD00078142, sumycin, tet-cy, quatrex, qidtet, unicin. |
| Q: What is the InChIKey of Tetracycline hydrochloride? |
| A: InChIKey of Tetracycline hydrochloride is YCIHPQHVWDULOY-FMZCEJRJSA-N. |
| Q: What is the safety information for Tetracycline hydrochloride? |
| A: Safety information for Tetracycline hydrochloride: S26-S36. |
| Q: What is the English name of Tetracycline hydrochloride? |
| A: The English name of Tetracycline hydrochloride is Tetracycline hydrochloride. |
| Q: What is the CAS number of Tetracycline hydrochloride? |
| A: CAS number of Tetracycline hydrochloride is 64-75-5. |
| Q: How is the water solubility of Tetracycline hydrochloride? |
| A: Water solubility of Tetracycline hydrochloride: 50 g/L. |
| Q: What are the uses of Tetracycline hydrochloride? |
| A: Main uses of Tetracycline hydrochloride: Tetracycline hydrochloride is a broad-spectrum antibiotic used to treat a wide range of infections. |
| Q: What is the LogP of Tetracycline hydrochloride? |
| A: LogP of Tetracycline hydrochloride is 1.28790. |
| Q: What is the boiling point of Tetracycline hydrochloride? |
| A: Boiling point of Tetracycline hydrochloride is 799.4ºC at 760 mmHg. |
This table lists manufacturers and suppliers of this compound, including vendor names and product supply reference information.
| Shanghai Nianxing Industrial Co., Ltd |
| Dayang Chem (Hangzhou) Co., Ltd. |
| Henan Tianfu Chemical Co., Ltd. |