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Fosfomycin tromethamine

CAS No.
78964-85-9
Chemical Name:
Fosfomycin tromethamine
Synonyms
FOSFOMYCIN TROMETAMOL;FOSFOMYCIN TROMETHAMOL;phosphomycin trometamol;tromethamine-fosfomycin;z1282;monuril;Fosfomycin tramine;Fosfomycin tromethanol;Fosfomycine Trometamol;fosfomycin tromethamine
CBNumber:
CB9365184
Molecular Formula:
C7H18NO7P
Molecular Weight:
259.19
MDL Number:
MFCD01706261
MOL File:
78964-85-9.mol
MSDS File:
SDS
Last updated:2026-01-13 11:27:13
Product description Number Pack Size Price
Fosfomycin trometamol European Pharmacopoeia (EP) Reference Standard F0400000 1500 mg $156
Fosfomycin trometamol 1286322 800mg $432
Fosfomycin trometamol European Pharmacopoeia (EP) Reference Standard F0400000 f0400000 $153
Fosfomycin Trometamol SML2512 20MG $125
Fosfomycin Trometamol ≥98% 23632 5mg $37
More product size

Fosfomycin tromethamine Properties

Melting point 122-125oC
storage temp. Hygroscopic, Refrigerator, under inert atmosphere
solubility Very soluble in water, slightly soluble in ethanol (96 per cent) and in methanol, practically insoluble in acetone.
form Solid
color White to Off-White
Stability Hygroscopic
Major Application pharmaceutical (small molecule)
InChI InChI=1/C4H11NO3.C3H7O4P/c5-4(1-6,2-7)3-8;1-2-3(7-2)8(4,5)6/h6-8H,1-3,5H2;2-3H,1H3,(H2,4,5,6)/t;2-,3+/s3
InChIKey QZJIMDIBFFHQDW-LMLSDSMGSA-N
SMILES C(N)(CO)(CO)CO.P([C@H]1O[C@H]1C)(O)(O)=O |&1:9,11,r|
FDA UNII 7FXW6U30GY
NCI Drug Dictionary fosfomycin tromethamine
UNSPSC Code 41116107
NACRES NA.24

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS08
Signal word  Danger
Hazard statements  H319-H317-H334-H315
Precautionary statements  P261-P272-P280-P302+P352-P333+P313-P321-P363-P501-P261-P285-P304+P341-P342+P311-P501-P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
WGK Germany  WGK 3
HS Code  2941906000
Storage Class 11 - Combustible Solids

Fosfomycin tromethamine price More Price(21)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich F0400000 Fosfomycin trometamol European Pharmacopoeia (EP) Reference Standard 78964-85-9 1500 mg $156 2025-07-31 Buy
Sigma-Aldrich 1286322 Fosfomycin trometamol 78964-85-9 800mg $432 2025-07-31 Buy
Sigma-Aldrich F0400000 Fosfomycin trometamol European Pharmacopoeia (EP) Reference Standard 78964-85-9 f0400000 $153 2024-03-01 Buy
Sigma-Aldrich SML2512 Fosfomycin Trometamol 78964-85-9 20MG $125 2023-06-20 Buy
Cayman Chemical 23632 Fosfomycin Trometamol ≥98% 78964-85-9 5mg $37 2024-03-01 Buy
Product number Packaging Price Buy
F0400000 1500 mg $156 Buy
1286322 800mg $432 Buy
F0400000 f0400000 $153 Buy
SML2512 20MG $125 Buy
23632 5mg $37 Buy

Fosfomycin tromethamine Chemical Properties,Uses,Production

Chemical Properties

White to off-white powder

Uses

Phosphonic acid derivative; antibacterial.

Uses

Fosfomycin Tromethamine is used as an antibiotic compound in the treatment of urinary tract infections.

Definition

ChEBI: Fosfomycin tromethamine is a phosphonoacetic acid.

brand name

Monurol (Zambon).

General Description

Fosfomycin tromethamine (Monurol) is a phosphonic acidepoxide derivative that was initially isolated from fermentationsof Streptomyces spp. Making the tromethamine salt greatly expanded the therapeutic utility of this antibacterial because water solubilityincreased enough to allow oral administration.
Fosfomycin is a broad-spectrum, bactericidal antibacterialthat inhibits the growth of E. coli, S. aureus, andSerratia, Klebsiella, Citrobacter, Enterococcus, andEnterobacter spp. at a concentration less than 64 mg/L.Currently fosfomycin is recommended as single-dose therapyfor uncomplicated urinary tract infections. It possessesin vitro efficacy similar to that of norfloxacin and trimethoprim-sulfamethoxazole.
Fosfomycin covalently inactivates the first enzyme in thebacterial cell wall biosynthesis pathway, UDP-N-acetylglucosamineenolpyruvyl transferase (MurA) by alkylation ofthe cysteine-115 residue. The inactivation reaction occursthrough nucleophilic opening of the epoxide ring. Resistanceto fosfomycin can occur through chromosomal mutationsthat result in reduced uptake or reduced MurA affinity for theinhibitor. Plasmid-mediated resistance mechanisms involveconjugative bioinactivation of the antibiotic with glutathione.The frequency of resistant mutants in in vitro studies hasbeen low, and there appears to be little cross-resistance betweenfosfomycin and other antibacterials.

Fosfomycin tromethamine Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 278)Suppliers
Supplier Tel Email Country ProdList Advantage
Nanjing Dorra Pharmaceutical Technology Co., Ltd
+86-15951889564 +86-025-82232955 info@dorrapharma.com China 29 58
Hebei Yanxi Chemical Co., Ltd.
+8618531123677 faithe@yan-xi.com China 5853 58
Hebei Chuanghai Biotechnology Co., Ltd
+8615531151365 mina@chuanghaibio.com China 18126 58
airuikechemical co., ltd.
+86-18353166132 sales02@airuikechemical.com China 983 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21595 55
Shanghai Yingrui Biopharma Co., Ltd.
+86-21-33585366 - 03@ sales03@shyrchem.com CHINA 738 60
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418679 +8618949832763 info@tnjchem.com China 2988 55
career henan chemical co
+86-0371-86658258 +8613203830695 sales@coreychem.com China 29830 58
Shandong chuangyingchemical Co., Ltd.
18853181302 sale@chuangyingchem.com CHINA 5906 58
Shanghai Yingrui Biopharma Co.,Ltd
21-33585366 export01@shyrchem.com CHINA 1319 58

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View Lastest Price from Fosfomycin tromethamine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Fosfomycin tromethamine pictures 2026-03-05 Fosfomycin tromethamine
78964-85-9
0.99 RongNa Biotechnology Co.,Ltd
Fosfomycin tromethamine pictures 2026-03-05 Fosfomycin tromethamine
78964-85-9
US $0.00 / Kg/Bag 1KG 98%-102%; EP 100KG WUHAN FORTUNA CHEMICAL CO., LTD
Fosfomycin tromethamine pictures 2025-12-01 Fosfomycin tromethamine
78964-85-9
US $0.00-0.00 / KG 1KG 98.0% 10000KGS Shaanxi Dideu New Materials Co. Ltd
(3-methyloxiranyl)-phosphonicaci(2r-cis)-phosphonicacicompd.with2-amino-2-(hydroxy fosfomycincompd.withtrometamol fosfomycintrometamolsalt methyl)-1,3-propanediol(1:1) Tromethamine fosfosmycin Fosfomycin Tromethamine (800 mg) FosfoMycin troMethaMine API Fosfomycin trometamolUSP, 98.0%-102.0% monuril z1282 fosfomycin tromethamine (2r-cis)-(3-methyloxiranyl)phosphonic acid compound with 2-amino-2-(hydroxymethyl)propane-1,3-diol (1:1) (1R,2S)-(1,2-Epoxypropyl)phosphonic acid, compound with 2-amino-2-(hyd roxymethyl)-1,3-propanediol (1:1) Fosfomycin Tromethaminel Fosfomycin tromethamine (MK-0955 tromethamine) Fosfomycin trometamol CRS Fosfomycin tromethamine USP/EP/BP Fosfomycin Trometamol Impurity 13 Fosfomycin TrometamolQ: What is Fosfomycin Trometamol Q: What is the CAS Number of Fosfomycin Trometamol Q: What is the storage condition of Fosfomycin Trometamol Q: What are the applications of Fosfomycin Trometamol Fosfomycin Tromethamine (1286322) FOSFOMYCIN TROMETAMOL FOSFOMYCIN TROMETHAMOL phosphomycin trometamol tromethamine-fosfomycin 2-Amino-2-(hydroxymethyl)propane-1,3-diol ((2R,3S)-3-methyloxiran-2-yl)phosphonate (Fosfomycin Impurity) Fosfomycin Tromethamine 2-amino-2-(hydroxymethyl)propane-1,3-diol ((2R,3S)-3- methyloxiran-2-yl) phosphonate 2-amino-2-(hydroxymethyl)propane-1,3-diol ((2R,3S)-3-methyloxiran-2-yl)phosphonate Fosfomycin tromethanol Fosfomycine Trometamol Fosfomycin tramine 2-Amino-2-(hydroxymethyl)-propan-1,3-diol ((2R,3S)-3-methyloxiran-2-yl)phosphonate 78964-85-9 156-2-90 8964-85-9 C4H11NO3C3H7O4P C7H18NO7P 25919 API Antibiotics