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KANAMYCIN B SULFATE

CAS No.
29701-07-3
Chemical Name:
KANAMYCIN B SULFATE
Synonyms
BEKANAMYCIN SULFATE;Kanendos;Stereocidin;KANAMYCIN B SULFATE;Aminodeoxybekanamycin;Kanamycin B sulfate CRS;KANAMYCIN B SULFATE SALT;BEKANAMYCIN SULFATE SALT;aminodeoxykanamycinsulfate;Kanamycin B Sulfate, EvoPure
CBNumber:
CB6761792
Molecular Formula:
C18H37N5O10.H2O4S
Molecular Weight:
581.59
MDL Number:
MFCD00078511
MOL File:
29701-07-3.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-20 15:45:18

KANAMYCIN B SULFATE Properties

storage temp. 2-8°C
solubility H2O: 50 mg/mL, clear, colorless
form powder
Merck 13,5299
BRN 5235274
Stability Hygroscopic
InChIKey YGTPKDKJVZOVCO-KELBJJLKSA-N
SMILES OS(O)(=O)=O.NC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O[C@H]3O[C@H](CO)[C@@H](O)[C@H](N)[C@H]3O)[C@H]2O)[C@H](N)[C@@H](O)[C@@H]1O
FDA UNII KB71EA86HM
UNSPSC Code 51281654
NACRES NA.85

SAFETY

Risk and Safety Statements

PPE Eyeshields, Gloves, type N95 (US)
Safety Statements  22-24/25
WGK Germany  2
RTECS  WK1976500
Storage Class 11 - Combustible Solids

KANAMYCIN B SULFATE price More Price(16)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich B5264 Kanamycin B sulfate salt aminoglycoside antibiotic 29701-07-3 100mg $140 2026-04-30 Buy
Sigma-Aldrich K0100000 Kanamycin B sulfate salt European Pharmacopoeia (EP) Reference Standard 20 mg $254 2026-04-30 Buy
Sigma-Aldrich B5264 Kanamycin B sulfate salt aminoglycoside antibiotic 29701-07-3 1g $788 2026-04-30 Buy
TRC TRC-K137515-25MG Kanamycin B Sulfate 29701-07-3 25mg $256 2026-06-03 Buy
TRC TRC-K137515-250MG Kanamycin B Sulfate 29701-07-3 250mg $1454 2026-06-03 Buy
Product number Packaging Price Buy
B5264 100mg $140 Buy
K0100000 20 mg $254 Buy
B5264 1g $788 Buy
TRC-K137515-25MG 25mg $256 Buy
TRC-K137515-250MG 250mg $1454 Buy

KANAMYCIN B SULFATE Chemical Properties, Uses, Production

Originator

Kanendomycin,Meiji Seika,Japan,1969

Uses

Antibiotic complex produced by Streptomyces kanamyceticus Okami & Umezawa from Japanese soil. Comprised of three components, kanamycin A, the major component, and kanamycins B and C, two minor congeners. Antibacterial.

Definition

ChEBI: Bekanamycin sulfate is an aminoglycoside sulfate salt. It is functionally related to a kanamycin B.

Manufacturing Process

200 liters of the medium containing 2.0% starch, 1.0% soybean meal, 0.05% KCl, 0.05% MgSO4·7H2O, 0.3% NaCl, 0.2% NaNO3 was placed in the 400 liter fermenter, the pH was adjusted to 7.5, and the medium was then sterilized (pH after the sterilization was 7.0) for 30 minutes at 120°C, inoculated with 1,000 ml of 40 hour shake-cultured broth of S. kanamyceticus (a selected subculture of K2-J strain) and tank-cultured at 27°-29°C. As antifoam,soybean oil (0.04%)and silicone (0.04%) were added. The broth after 48 hours was found to contain 250 mcg/ml of kanamycin.
A portion (950 ml) of the rich eluate was adjusted to pH 6.0 by the addition of sulfuric acid. Ultrawet K (7.0 g) in 70 ml water was added slowly to the neutralized eluate to precipitate kanamycin B dodecylbenzenesulfonate which was collected by filtration after adding filter aid (Dicalite). The cake was washed with water and extracted with 100 ml methanol. After filtering and washing with methanol, sulfuric acid was added to the filtrate until no more kanamycin B sulfate precipitated. After addition of an equal volume of acetone to provide more complete precipitation, the kanamycin B sulfate was collected by filtration, washed with methanol and dried in vacuo at 50°C.

Therapeutic Function

D-Streptamine, O-3-amino-3-deoxy-α-D-glucopyranosyl-(1- 6)-O-[2,6-diamino-2,6-dideoxy-α-D-glucopyranosyl-(1-4)]-2-deoxy sulfate (1:1)

Purification Methods

A small quantity of kanamycin B (24mg) can be purified on a small Dowex-1 x 2 column (6 x 50mm); the required fraction is evaporated to dryness and the residue crystallised from EtOH containing a small amount of H2O. [Umezawa et al. Bull Chem Soc Jpn 42 537 1969.] It has been crystallised from H2O by dissolving ~1g in H2O (3mL), adding Me2NCHO (3mL) and setting aside at 4o overnight. The needles are collected and dried to constant weight at 130o. It has also been recrystallised from aqueous EtOH. It is slightly soluble in CHCl3 and isoPrOH. [IR: Wakazawa et al. J Antibiot 14A 180, 187 1961, Ito et al. J Antibiot 17 A 189 1964, Beilstein 18 III/IV 7631.]

KANAMYCIN B SULFATE Preparation Products And Raw materials

Raw materials

Preparation Products

KANAMYCIN B SULFATE Suppliers

Global Suppliers ( 52)
Supplier Tel Email Country ProdList Advantage
Shanghai Boyle Chemical Co., Ltd. sales@boylechem.com China 2915 55
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Chemsky (shanghai) International Co.,Ltd 021-50135380 shchemsky@sina.com China 15350 60
Beijing HuaMeiHuLiBiological Chemical 010-56205725 waley188@sohu.com China 12323 58
Shanghai Kewel Chemical Co., Ltd. 021-64609169 18901607656 greensnown@163.com China 9883 50
Alfa Chemistry 1-516-6625404 support@alfa-chemistry.com United States 9170 60
Shanghai EFE Biological Technology Co., Ltd. 021-65675885 18964387627 info@efebio.com China 9799 58
UHN Shanghai Research & Development Co., Ltd. 021-58958002 18930822973 sales@uhnshanghai.com China 1983 58
Shenzhen Polymeri Biochemical Technology Co., Ltd. +86-400-002-6226 sales@rrkchem.com China 57336 58
TOSUN PHARM 020-66392521-118 18922260391 3004261881@qq.com China 7994 58
aminodeoxykanamycinsulfate kanamycinb,sulfate(1:1)(salt) BEKANAMYCIN SULFATE SALT KANAMYCIN B SULFATE KANAMYCIN B SULFATE SALT Aminodeoxybekanamycin Kanamycin B sulfate CRS KANAMYCIN B SULFATE USP/EP/BP Kanendos Stereocidin kanamycin B sulfate (Amikacin EP Impurity D) Kanamycin B Sulfate, EvoPure D-Streptamine, O-3-amino-3-deoxy-α-D-glucopyranosyl-(1→6)-O-[2,6-diamino-2,6-dideoxy-α-D-glucopyranosyl-(1→4)]-2-deoxy-, sulfate (1:1) BEKANAMYCIN SULFATE 29701-07-3 29701-10-3 C18H37N5O10H2O4S C18H37N5O10H2SO4 C18H39N5O14S Antibiotics Antibiotics G-M Antibiotics A to Z BioChemical Amines Intermediates & Fine Chemicals Oligosaccharides Pharmaceuticals