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Dicloxacillin sodium

CAS No.
13412-64-1
Chemical Name:
Dicloxacillin sodium
Synonyms
Dicloxacillin sodium;Dicloxacillin sodium RS;Dicloxacillin sodium CRS;DICLOXACILLIN SODIUM USP;Dicloxacillin Sodium (500 mg);Dicloxacillin Sodium (300 mg);icloxacillinsodiummonohydrate;Dicloxacillin sodium USP/EP/BP;Dicloxacillin Sodium (1189009);DICLOXACILLIN SODIUM WHO(CRM STANDARD)
CBNumber:
CB4679268
Molecular Formula:
C19H20Cl2N3NaO6S
Molecular Weight:
512.33
MDL Number:
MFCD00167147
MOL File:
13412-64-1.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-16 07:06:08

Dicloxacillin sodium Properties

Melting point 222-225°C
alpha D20 +127.2° (water)
storage temp. 2-8°C
solubility H2O: soluble50mg/mL
form powder
color white to off-white
Water Solubility Soluble in water
BRN 4778711
Stability Hygroscopic
Major Application clinical testing
InChIKey SIGZQNJITOWQEF-VICXVTCVSA-M
SMILES [Na+].[H]O[H].Cc1onc(c1C(=O)N[C@H]2[C@H]3SC(C)(C)[C@@H](N3C2=O)C([O-])=O)-c4c(Cl)cccc4Cl
CAS DataBase Reference 13412-64-1(CAS DataBase Reference)
FDA UNII 4HZT2V9KX0
UNSPSC Code 51102829
NACRES NA.85

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)Health Hazard (GHS08)
GHS07,GHS08
Signal word  Danger
Hazard statements  H315-H319-H334-H335
Precautionary statements  P261-P264-P271-P302+P352-P304+P340+P312-P305+P351+P338
target organs Respiratory system
PPE dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Hazard Codes  Xn
Risk Statements  36/37/38-42/43
Safety Statements  22-26-36/37-45
WGK Germany  2
RTECS  XH8925000
HS Code  29411099
Storage Class 11 - Combustible Solids
Hazard Classifications Eye Irrit. 2
Resp. Sens. 1
Skin Irrit. 2
STOT SE 3
Toxicity LD50 in mice (g/kg): 0.9 i.v.; in rats (g/kg): 0.63 i.p.; >5 orally (Gloxhuber)
NFPA 704
0
2 0

Dicloxacillin sodium price More Price(49)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich D1050000 Dicloxacillin sodium European Pharmacopoeia (EP) Reference Standard 13412-64-1 250 mg $167 2026-04-30 Buy
Sigma-Aldrich 46182 Dicloxacillin sodium salt hydrate VETRANAL 13412-64-1 100mg $63.6 2026-04-30 Buy
Sigma-Aldrich 1189009 Dicloxacillin sodium United States Pharmacopeia (USP) Reference Standard 13412-64-1 300mg $466 2026-04-30 Buy
Cayman Chemical 23770 Dicloxacillin (sodium salt hydrate) ≥98% 13412-64-1 1g $63 2026-04-30 Buy
Cayman Chemical 23770 Dicloxacillin (sodium salt hydrate) ≥98% 13412-64-1 5g $229 2026-04-30 Buy
Product number Packaging Price Buy
D1050000 250 mg $167 Buy
46182 100mg $63.6 Buy
1189009 300mg $466 Buy
23770 1g $63 Buy
23770 5g $229 Buy

Dicloxacillin sodium Chemical Properties,Uses,Production

Brand Name(s) in US

Dynapen

Chemical Properties

White to off-white crystalline powder

Originator

Dynapen,Bristol,US,1968

Uses

Dicloxacillin sodium salt is used in the treatment of staphylococci resistant to penicillin G. Dicloxacillin binds to specific penicillin-binding proteins in the bacterial cell wall and therefore inhibits the last stage of bacterial cell wall synthesis. Cell lysis, mediated by bacterial cell wall autolytic enzymes, is the result. Dicloxacillin may interfere with autolysin inhibitors.

Uses

A semi-synthetic antibiotic related to Penicillin. Antibacterial.

Uses

Antibacterial;Bacterial transpeptidase inhibitor

Definition

ChEBI: Dicloxacillin sodium monohydrate is a hydrate. It contains a dicloxacillin sodium.

Manufacturing Process

A suspension of 6-aminopenicillanic acid (216 grams) in water (2 liters) was adjusted to pH 6.8 by the addition of N aqueous sodium hydroxide (approximately 1 liter) and the resulting solution was stirred vigorously while a solution of 3-(2',6'-dichlorophenyl)-5-methylisoxazole-4-carbonyl chloride (290 grams) in acetone (1.5 liters) was added in one portion.
The temperature rose to 26°C and as reaction proceeded the free acid form of the penicillin separated as a white solid. After 30 minutes the suspension was cooled to 10°C and stirring was continued at this temperature for 1 hour more. The mixture was then cooled to 0°C, centrifuged, and the solid product washed with aqueous acetone (250 ml) and finally dried in an air oven at 30°C. The product (440 grams, 94%) had [α]D20 +106.3° (c 1 in EtOH) and was shown by alkalimetric assay to be 97.5% pure.
The salt was prepared by dissolving the free acid form of the penicillin in the equivalent amount of aqueous sodium bicarbonate and freeze drying the resulting solution. The hydrated salt so obtained was shown by alkalimetric assay to be 94% pure and to contain 6% water.

brand name

Dynapen (Apothecon).

Therapeutic Function

Antibacterial

General Description

The substitution of chlorine atoms on both carbons orthoto the position of attachment of the phenyl ring to the isoxazolering is presumed to enhance further the stability ofthe oxacillin congener dicloxacillin sodium, [3-(2,6-dichlorophenyl)-5-methyl-4-isoxazolyl]penicillin sodiummonohydrate (Dynapen, Pathocil, Veracillin) and toproduce high plasma concentrations of it. Its medicinalproperties and use are similar to those of cloxacillinsodium. Progressive halogen substitution, however, alsoincreases the fraction bound to protein in the plasma, potentiallyreducing the concentration of free antibiotic inplasma and tissues. Its medicinal properties and use are thesame as those of cloxacillin sodium.

Biological Activity

Docloxacillin binds to specific penicillin-binding proteins (PBPs) in the bacterial cell wall and therefore inhibits the last stage of bacterial cell wall synthesis. Cell lysis, mediated by bacterial cell wall autolytic enzymes, is the result. Dicloxacillin may interfere with autolysin inhibitors .

Veterinary Drugs and Treatments

The veterinary use of dicloxacillin has been primarily in the PO treatment of bone, skin, and other soft tissue infections in small animals when penicillinase-producing Staphylococcus species have been isolated. Because of its low oral bioavailability and short halflife, other drugs with good staph coverage are usually employed.

Global( 262)Suppliers
Supplier Tel Email Country ProdList Advantage
Nanjing Lirui Pharmaceutical Trading Co., Ltd. 15951922363 wendy@lyripharma.com China 500 58
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
3B Pharmachem (Wuhan) International Co.,Ltd. 18930552037 3bsc@sina.com China 15813 69
Shanghai Hanhong Scientific Co.,Ltd. 021-54306202 13764082696 info@hanhongsci.com China 42917 64
Chemsky(shanghai)International Co.,Ltd. 021-50135380 shchemsky@sina.com China 32273 50
Sinopharm Chemical Reagent Co,Ltd. 86-21-63210123 sj_scrc@sinopharm.com China 9791 79
Dalian Meilun Biotech Co., Ltd. 0411-62910999 13889544652 sales@meilune.com China 4765 58
Beijing HuaMeiHuLiBiological Chemical 010-56205725 waley188@sohu.com China 12323 58
Haoyuan Chemexpress Co., Ltd. 021-58950125 info@chemexpress.com China 7545 61
MedChemexpress LLC 021-58955995 sales@medchemexpress.cn United States 4853 58

View Lastest Price from Dicloxacillin sodium manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Dicloxacillin Sodium hydrate pictures 2026-07-15 Dicloxacillin Sodium hydrate
13412-64-1
$50.00-72.00 97.77% 10g TargetMol Chemicals Inc.
Dicloxacillin Sodium hydrate pictures 2026-07-15 Dicloxacillin Sodium hydrate
13412-64-1
$50.00-72.00 97.77% 10g TargetMol Chemicals Inc.
Dicloxacillin sodium pictures 2026-03-20 Dicloxacillin sodium
13412-64-1
$10.00 100KG 99% 100 mt Hebei Chuanghai Biotechnology Co., Ltd

Dicloxacillin sodium Spectrum

3-(2,6-DICHLOROPHENYL)-5-METHYL-4-ISOXAZOLYL PENICILLIN DICLOXACILLIN SODIUM SALT HYDRATE VETRAN DICLOXACILLIN SODIUM EPD(CRM STANDARD) DICLOXACILLIN SODIUM USP(CRM STANDARD) DICLOXACILLIN SODIUM WHO(CRM STANDARD) Dicloxacillin monohydrate sodium salt Dicloxacillin sodium Sodium 7-[3-(2,6-dichlorophenyl)-5-methyl-oxazol-4-yl]carbonylamino-3,3-dimet hyl-6-oxo-2-thia-5-azabicyclo[3.2.0]heptane-4-carboxylate 4-Thia-1-azabicyclo3.2.0heptane-2-carboxylic acid, 6-3-(2,6-dichlorophenyl)-5-methyl-4-isoxazolylcarbonylamino-3,3-dimethyl-7-oxo-, monosodium salt, monohydrate, (2S,5R,6R)- Dicloxacillin sodium monohydrate/Mesterolone Monosodium (2S,5R,6R)-6-(3-(2,6-dichlorophenyl)-5-methyl-4-isoxazolecarboxamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate (2S,5R,6R)-6-[[[3-(2,6-Dichlorophenyl)-5-Methyl-4-isoxazolyl]carbonyl]aMino]-3,3- diMethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid SodiuM Salt Hydrate Dicloxacillin Sodium (500 mg) 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylicacid,6-[[[3-(2,6-dichlorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-,sodium salt, hydrate Dicloxacillin Sodium (300 mg) Dicloxacillin sodium hydrate solution,100ppm Dicloxacillin Sodium Salt Monohydrate Standard Dicloxacillin sodium CRS icloxacillinsodiummonohydrate Dicloxacillin sodium USP/EP/BP Dicloxacillin Sodium (1189009) Dicloxacillin Sodium hydrate,Dicloxacillin sodium salt,inhibit,Antibiotic,Bacterial,sepsis,peritonitis,Inhibitor,Dicloxacillin Sodium Sodium (2S,5R,6R)-6-(3-(2,6-dichlorophenyl)-5-methylisoxazole-4-carboxamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate hydrate Dicloxacillin sodium hydrate in ACN:H2O (9:1) C12560500 Dicloxacillin sodium hydrate DICLOXACILLIN SODIUM USP Dicloxacillin sodium RS 13412-64-1 3412-64-1 C19H18Cl2N3NaO6S C19H16Cl2N3O5SNaxH2O C19H16Cl2N3NaO5SxH2O C19H17Cl2N3O5SNa C19H16Cl2N3NaO5SH2O Diclocil Peptide Synthesis/Antibiotics Aromatics Chiral Reagents Heterocycles Intermediates & Fine Chemicals Pharmaceuticals Sulfur & Selenium Compounds APIs A - KAntibiotics Antibacterial Antibiotics A to Antibiotics A-FAntibiotics Chemical Structure Class Interferes with Cell Wall SynthesisAntibiotics Mechanism of Action Penicillins and Cephalosporins (beta-Lactams) Spectrum of Activity