ChemicalBook >> CAS DataBase List >>Metacycline hydrochloride

Metacycline hydrochloride

CAS No.
3963-95-9
Chemical Name:
Metacycline hydrochloride
Synonyms
METACYCLINE;METHACYCLINE HYDROCHLORIDE;METHACYCLINE HCL;METACYCLINE HCL;optimycin;MethacycL;metadomus;londomycin;megamycine;adriamicina
CBNumber:
CB2355197
Molecular Formula:
C22H23ClN2O8
Molecular Weight:
478.88
MDL Number:
MFCD04972012
MOL File:
3963-95-9.mol
MSDS File:
SDS
Last updated:2026-01-30 18:09:56
Product description Number Pack Size Price
Methacycline hydrochloride Pharmaceutical Secondary Standard; Certified Reference Material PHR1594 1g $186
Methacycline hydrochloride United States Pharmacopeia (USP) Reference Standard 1397006 200mg $376
Methacycline (hydrochloride) ≥98% 21338 1g $32
Methacycline (hydrochloride) ≥98% 21338 5g $63
Methacycline (hydrochloride) ≥98% 21338 10g $93
More product size

Metacycline hydrochloride Properties

Melting point >224°C(dec.)
storage temp. Inert atmosphere,Room Temperature
solubility DMSO (Slightly, Heated), Methanol (Slightly, Heated, Sonicated), Water (Slightly)
form Crystalline Powder
color Yellow
BRN 5470951
Major Application pharmaceutical (small molecule)
InChIKey VZQARNDJLLWXGL-ATGQEJIKNA-N
SMILES O[C@@]12C(C(C(=O)N)=C(O)[C@@H](N(C)C)[C@]1([H])[C@H]([C@]1([H])C(C3C=CC=C(O)C=3C(=O)C1=C2O)=C)O)=O.Cl |&1:1,9,13,15,16,r|
CAS DataBase Reference 3963-95-9
FDA UNII 9GJ0N7ZAP0
ATC code J01AA05
Proposition 65 List Methacycline Hydrochloride
EPA Substance Registry System Methacycline hydrochloride (3963-95-9)
UNSPSC Code 41116107
NACRES NA.24

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H335-H319
Precautionary statements  P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
Safety Statements  24/25-22
WGK Germany  2
RTECS  QI9276000
HS Code  29413020
Storage Class 11 - Combustible Solids
Toxicity LD50 in rats, mice (mg/kg): 252, 288 i.p. (Goldenthal)
NFPA 704
0
2 0

Metacycline hydrochloride price More Price(22)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich PHR1594 Methacycline hydrochloride Pharmaceutical Secondary Standard; Certified Reference Material 3963-95-9 1g $186 2025-07-31 Buy
Sigma-Aldrich 1397006 Methacycline hydrochloride United States Pharmacopeia (USP) Reference Standard 3963-95-9 200mg $376 2025-07-31 Buy
Cayman Chemical 21338 Methacycline (hydrochloride) ≥98% 3963-95-9 1g $32 2024-03-01 Buy
Cayman Chemical 21338 Methacycline (hydrochloride) ≥98% 3963-95-9 5g $63 2024-03-01 Buy
Cayman Chemical 21338 Methacycline (hydrochloride) ≥98% 3963-95-9 10g $93 2024-03-01 Buy
Product number Packaging Price Buy
PHR1594 1g $186 Buy
1397006 200mg $376 Buy
21338 1g $32 Buy
21338 5g $63 Buy
21338 10g $93 Buy

Metacycline hydrochloride Chemical Properties,Uses,Production

Description

Methacycline is a tetracycline-class antibiotic that is active against a wide range of Gram-positive and Gram-negative organisms. It is readily absorbed from the gastrointestinal tract and reaches a maximum concentration at about the fourth hour, declining to a negligible amount in about 24 hours. It is more active than tetracycline against a number of bacteria.

Chemical Properties

yellow crystalline powder

Originator

Rondomycin ,Pfizer ,UK ,1963

Uses

Broad spectrum, semisynthetic antibiotic related to Tetracycline. Antibacterial.

Uses

analgesic, narcotic antagonist

Uses

Methacycline hydrochloride is a salt prepared from methacycline taking advantage of the basic dimethylamino group which protonates and readily forms a salt in hydrochloric acid solutions. The hydrochloride is the preferred formulation for pharmaceutical applications. Like all tetracyclines, methacycline hydrochloride shows broad spectrum antibacterial and antiprotozoan activity and acts by binding to the 30S and 50S ribosomal subunits, blocking protein synthesis.

Uses

A broad spectrum, anti bacterial, semisynthetic antibiotic related to Tetracycline

Definition

ChEBI: Methacycline hydrochloride is an organic molecular entity.

Manufacturing Process

To a stirred solution of 4.6 g (0.01 mol) of anhydrous oxytetracycline in 40 ml of dry tetrahydrofuran is added 3.5 g (0.021 mol) of pyridine-sulfur trioxide complex. After 16 hours of stirring at room temperature, the resulting suspension is filtered, and the solid is slurried with 25 ml of 2% hydrochloric acid for 10 minutes, filtered and thoroughly washed with methanol followed by ether. The pale yellow crystalline 5-oxytetracycline-6,12-hemiketal-12-sulfuric acid ester melts at 210°C.
500 mg 5-oxytetracycline-6,12-hemiketal-12-sulfuric acid ester, prepared as described, is added to 4 ml dry liquid hydrogen fluoride, and the mixture is stirred for 1.5 hours at ice bath temperature. The hydrogen fluoride is then evaporated in a stream of nitrogen and the resulting gummy solids are triturated with about 15 ml ether and filtered. The resulting solid hydrofluoride salt is further purified by suspending in water, adjusting the pH to about 4, and extracting the 6-methylene-5-oxytetracycline free base from the aqueous phase with ethyl acetate. The extract is separated and evaporated to dryness under reduced pressure. The resulting residue is triturated with ether and filtered, and the solid is recrystallized from methanol-acetone-etherconcentrated hydrochloric acid to obtain the product as a purified hydrochloride, according to US Patent 3,026,354.

brand name

Rondomycin (Medpointe).

Therapeutic Function

Antibiotic

General Description

The synthesis of methacycline, 6-deoxy-6-demethyl-6-methylene-5-oxytetracycline hydrochloride (Rondomycin), reportedby Blackwood et al. in 1961, was accomplished bychemical modification of oxytetracycline. It has an antibioticspectrum like that of the other tetracyclines but greater potency;about 600 mg of methacycline is equivalent to 1 g oftetracycline. Its particular value lies in its longer serum halflife;doses of 300 mg produce continuous serum antibacterialactivity for 12 hours. Its toxic manifestations and contraindicationsare similar to those of the other tetracyclines.
The greater stability of methacycline, both in vivo and invitro, results from modification at C-6. Removal of the 6-hydroxy group markedly increases the stability of ring C toboth acids and bases, preventing the formation of isotetracyclinesby bases. Anhydrotetracyclines still can form, however,by acid-catalyzed isomerization under strongly acidicconditions. Methacycline hydrochloride is a yellow to darkyellow, crystalline powder that is slightly soluble in waterand insoluble in nonpolar solvents. It should be stored intight, light-resistant containers in a cool place.

References

[1] E G HUBERT. Activity of methacycline, related tetracyclines, and other antibiotics against various L-forms and their parent bacteria in vitro.[J]. Antimicrobial Agents and Chemotherapy, 1972, 2 4: 276-280. DOI: 10.1128/aac.2.4.276
[2] R S MORTON  D W H. Methacycline (rondomycin) in gonorrhoea.[J]. The British Journal of Venereal Diseases, 1966, 42 3: 175-177. DOI: 10.1136/sti.42.3.175
[3] DAVID G MCLONE. Gonorrheal urethritis in men treated with one oral dose of methacycline.[J]. Public health reports (Washington, D.C.?: 1896), 1968, 83 1: 87-89.

Metacycline hydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 305)Suppliers
Supplier Tel Email Country ProdList Advantage
HEBEI SHENGSUAN CHEMICAL INDUSTRY CO.,LTD
+86-15350851019; +8615350851019 admin@86-ss.com China 999 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21599 55
career henan chemical co
+86-0371-86658258 +8613203830695 sales@coreychem.com China 29833 58
BOC Sciences
+1-631-485-4226 inquiry@bocsci.com United States 19552 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49977 58
Neostar United (Changzhou) Industrial Co., Ltd.
+86-0519-85551759 +8613506123987 marketing1@neostarunited.com China 8830 58
TargetMol Chemicals Inc.
+1-781-999-5354; +17819995354 marketing@targetmol.com United States 32470 58
Hebei Miaobian Biotechnology Co., Ltd
+8617733850068 CHINA 967 58
Longyan Tianhua Biological Technology Co., Ltd
0086 18039857276 18039857276 CHINA 2783 58
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418671 +8618949823763 sales@tnjchem.com China 34563 58

View Lastest Price from Metacycline hydrochloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Methacycline hydrochloride pictures 2026-01-30 Methacycline hydrochloride
3963-95-9
US $52.00 / mg 99.50% 10g TargetMol Chemicals Inc.
Methacycline hydrochloride pictures 2026-01-30 Methacycline hydrochloride
3963-95-9
US $52.00 / mg 99.50% 10g TargetMol Chemicals Inc.
Metacycline hydrochloride pictures 2026-01-30 Metacycline hydrochloride
3963-95-9
US $0.00 / Kg/Drum 1KG 98%min 1000kg WUHAN FORTUNA CHEMICAL CO., LTD

Metacycline hydrochloride Spectrum

Methacycline HCl (PhysioMycine) Rondomycin hydrochloride 6-Methyleneoxytetracycline hydrochloride, Metacycline hydrochloride, LondoMycin (4S,4aR,5S,5aR,12aS)- 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methylene-1,11-dioxo-2-naphthacenecarboxamide, hydrochloride (1:1) Methacycline hydrochloride Solution, 100ppm Hydrochloric acid methacycline 6-DEMETHYL-6-DEOXY-6-METHYLENEOXYTETRACYCLINE MONOHYDROCHLORIDE 6-DEMETHYL-6-DEOXY-6-METHYLENEOXYTETRACYCLNE HYDROCHLORIDE METACYCLINE METACYCLINE HCL METACYCLINE HYDROCHLORIDE METHACYCLINE HCL METHACYCLINE HYDROCHLORIDE 12,12a-pentahydroxy-6-methylene-1,11-dioxo-1monohydrochloride metilenbiotic optimycin physiomycine Metacycline hydrochloride, sec. Standard, 98% 2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methylene-1,11-dioxo-, monohydrochloride, (4S,4aR,5S,5aR,12aS)- METHACYCLINE HYDROCHLORIDE (METACYCLINE HYDROCHLORIDE) METACYCLINE HYDROCHLORIDE, 98%, SEC. STANDARD MethacycL Methacycline hydrochlorid 2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methylene-1,11-dioxo-, monohydrochloride Metacycline, Adramycin, Rondomycin, Pindex Methacycline hydrochloride, potency: 877 u/mg Metacylcline HLC (4S,4aR,5S,5aR,12aS)-4-(DiMethylaMino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-Methylene-1,11-dioxo-2-naphthacenecarboxaMide HCl Methacycline hydrochloride (PhysioMycine) adriamicina ciclobiotic germiciclin globociclina londomycin megamycine metadomus methacyclinemonohydrochloride Metacyclin hydrochloride Methacycline Hydrochloride (200 mg) Methacycline Hydrochloride (200 mg)I0C348903ug/mg(ai) Metacycline hydrochloride USP/EP/BP (4S,4aR,5S,5aR,12aS)-4-(Dimethylamino)-3,5,10,12,12a-pentahydroxy-6-methylene-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydrotetracene-2-carboxamide hydrochloride Methacycline HydrochlorideQ: What is Methacycline Hydrochloride Q: What is the CAS Number of Methacycline Hydrochloride Q: What is the storage condition of Methacycline Hydrochloride Q: What are the applications of Methacycline Hydrochloride Metacyclinhydrochlorid Methacycline Hydrochloride (1397006) Doxycycline EP Impurity B / Methacycline Impurity Doxycycline Hyclate Impurity B as Hydrochloride Doxycycline Hyclate EP Impurity B as Hydrochloride (4S,4Ar,5S,5aR,12aS)-4-(dimethylamino)-1,5,10,11,12a-pentahydroxy-6-methylidene-3,12-dioxo-4,4a,5,5a-tetrahydrotetracene-2-carboxamide Doxycycline EP Impurity B(HCl) Methicycline hydrochloride Methacylcycline Hydrochloride C14917000 MetacyclinEhydrochloride Methacycline hydrochloride 100 μg/ml Acetonitrile Methacycline hydrochloride, 10 mM in DMSO DOXYCYCLINE EP IMPURITY B (METHACYCLINE HCL) Metacycline hydrochloride 100 μg/mL in Acetonitrile Metacycline hydrochloride RS