Sulfaguanidine
- CAS No.
- 57-67-0
- Chemical Name:
- Sulfaguanidine
- Synonyms
- SG;SULPHAGUANIDINE;4-amino-N-carbamimidoylbenzenesulfonamide;SULFAQUANIDINE;Sulfoguanidine;50DAG;A-307;Diacta;Sulgin;rp2275
- CBNumber:
- CB7152799
- Molecular Formula:
- C7H10N4O2S
- Molecular Weight:
- 214.24
- MDL Number:
- MFCD00038136
- MOL File:
- 57-67-0.mol
| Melting point | 190-193°C |
|---|---|
| Boiling point | 426.1±47.0 °C(Predicted) |
| Density | 1.3916 (rough estimate) |
| refractive index | 1.6440 (estimate) |
| storage temp. | Keep in dark place,Inert atmosphere,Room temperature |
| solubility | 1 M HCl: soluble50mg/mL |
| form | Powder |
| pka | pKa 2.37(H2O t = 37) (Uncertain) |
| color | white to off-white |
| Water Solubility | 1g/1000mL at 25 ºC |
| Merck | 14,8908 |
| BRN | 2695326 |
| Stability | Stable. Incompatible with strong oxidizing agents. |
| CAS DataBase Reference | 57-67-0(CAS DataBase Reference) |
| FDA UNII | 15XQ8043FN |
| NIST Chemistry Reference | Sulfaguanidine(57-67-0) |
| ATC code | A07AB03 |
| EPA Substance Registry System | Benzenesulfonamide, 4-amino-N-(aminoiminomethyl)- (57-67-0) |
SAFETY
Risk and Safety Statements
| Symbol(GHS) |  GHS07 |
|||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Signal word | Warning | |||||||||
| Hazard statements | H315-H319-H335 | |||||||||
| Precautionary statements | P261-P264-P271-P280-P302+P352-P305+P351+P338 | |||||||||
| Hazard Codes | Xi | |||||||||
| Risk Statements | 36/37/38 | |||||||||
| Safety Statements | 26-36 | |||||||||
| RIDADR | 3249 | |||||||||
| WGK Germany | 3 | |||||||||
| RTECS | WO8575000 | |||||||||
| F | 10 | |||||||||
| HazardClass | 6.1(b) | |||||||||
| PackingGroup | III | |||||||||
| HS Code | 29350090 | |||||||||
| NFPA 704 |
|
Sulfaguanidine price More Price(19)
| Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|---|
| Sigma-Aldrich | S8751 | Sulfaguanidine | 57-67-0 | 25g | $57.1 | 2024-03-01 | Buy |
| Sigma-Aldrich | 32402 | Sulfaguanidine VETRANAL | 57-67-0 | 100mg | $86.7 | 2024-03-01 | Buy |
| TCI Chemical | S0464 | Sulfaguanidine >98.0%(HPLC)(T) | 57-67-0 | 25g | $23 | 2024-03-01 | Buy |
| TCI Chemical | S0464 | Sulfaguanidine >98.0%(HPLC)(T) | 57-67-0 | 500g | $126 | 2024-03-01 | Buy |
| Sigma-Aldrich | S1975600 | Sulfaguanidine European Pharmacopoeia (EP) Reference Standard | 57-67-0 | s1975600 | $220 | 2024-03-01 | Buy |
Sulfaguanidine Chemical Properties,Uses,Production
sulfanilamide drugs
Sulfa and Sulfaguanidine have been ever common sulfa drugs. Owing to its relative high toxicity, it is generally not used as the drug of first choice, now they, together with acetaminophen chloride are only used as the intermediates of the manufacturing of sulfa drugs.
Sulfaguanidine is used as sulfa drugs for the treatment of intestinal infections in the earliest time. The molecular structure of sulfaguanidine contains a strongly basic guanidine group with high dissociation property and low lipid solubility. Although there is certain amount which can be absorbed through the gut after oral administration, the amount is not enough to achieve an effective blood concentration, therefore not being used for systemic infections. However, it can be maintained at a high concentration in the intestines, mostly used for the treatment of bacterial infections in the digestive tract such as gastroenteritis and dysentery. When being used in combination with antibacterial synergist trimethoprim (TMP) or di-trimethoprim (DVD), its antibacterial effect was significantly enhanced.
Preparation methods:
1. the finished product of sulfaguanidine can be made through the melting of sulfa and guanidine nitrate in the soda and further vacuum condensation.
2. it can be alternatively made from the reaction between acesulfame chloride and guanidine nitrate in the mixed solution of acetone and water in the presence of sodium hydroxide.
3. take p-nitrobenzenesulfonyl chloride as raw material, go through catalytic hydrogenation reaction to produce p-amino benzenesulfonyl chloride and further ammoniation to generate sulfonamides, and then reacted with guanidine nitrate to obtain sulfaguanidine.
Drug interactions:
1. Simultaneous administration of urine alkaline drugs can enhance the solubility of this product in alkaline urine and increase the excretion.
2. Sulfaguanidine can’t be used in combination with 4-aminobenzoic acid which can replace this product to be absorbed by bacteria and is mutually antagonistic with each other. It is also not suitable to be used in combination with local anesthetics drugs containing the p-amino-benzoyl group such as procaine, tetracaine and so on.
3. for patients subjecting to administration of estrogen contraceptives, simultaneously prolonged administration can lead to a reduction of the reliability of Sulfaguanidine contraceptive and also increase the chance of non-menstrual bleeding.
4. being used in combination with the light-sensitive drug effect may cause photosensitive additive effect.
5. people subjecting to the treatment of goods have a high demand for vitamin K.
This information is edited by Xiongfeng Dai from Chemicalbook.
Chemical Properties
It appears as needle-like crystalline powder with the melting point being 190-193 ℃. 1g of this product can be dissolved in about 1000 ml of water at 25 ℃, dissolved in about 10 ml of water at 100 ℃. It is slightly soluble in ethanol or acetone and easily soluble in dilute hydrochloric acid. It is odorless and tasteless with its color deepened in the case of light.
Uses
1. It belongs to sulfa drugs and used for the treatment of bacillary dysentery and enteritis.
2. It can be used for the treatment of intestinal antibacterial infections such as bacterial dysentery enteritis and can also be used to prevent infection before bowel surgery.
3. It is the first-choice of drug for the treatment of leprosy, being suitable for the treatment of various types of leprosy and being able to alleviate the clinical symptoms. It can generally alleviate the mucosal lesions rapidly with the improvement of skin lesions occurring more slowly, with even slower rate in neuropathy, thereby leading to long course. It is easy to produce drug resistance and difficult to cure. In addition, it can also be used for the treatment of dermatitis herpetiformis, lupus, psoriasis, foot fungus disease and malaria. Its preparation is tablet.
Production methods
It can be made through the condensation between sulfa and guanidine nitrate.
Category
Toxic substances.
Toxicity grading
Poisoning.
Acute toxicity
Intraperitoneal-mouse LDL0: 500 mg/kg.
Flammability and hazardous characteristics
It is combustible with combustion producing toxic fumes of nitrogen oxides and sulfur oxides.
Storage characteristics
Treasury: ventilated, low-temperature and dry.
Extinguishing agent
Dry powder, foam, sand, carbon dioxide, water mist.
Chemical Properties
white powder
Originator
Sulfaguanidine,Lederle,US,1941
Uses
Sulfonamide antibacterial.
Uses
Sulfaguanidine is a sulfonamide based antibiotic drug with potential application in veterinary medicine.
Definition
ChEBI: Sulfaguanidine is a sulfonamide incorporating a guanidine moiety used to block the synthesis of folic acid; mostly used in veterinary medicine It has a role as an antiinfective agent.
Manufacturing Process
10 parts of guanidine hydrochloride (0.1 mol) was dissolved in 75 parts of
water and the pH adjusted to 8 to 9. The solution was warmed to 50°C to
60°C and kept at this temperature while a slurry of 25 parts (0.113 mol) of pnitrobenzenesulfonyl
chloride was added slowly with mechanical stirring. The
pH was kept at 8 to 9 by the addition of 40% sodium hydroxide solution. At
the end of the reaction the solution was cooled and filtered from the
separated solid. The p-nitrobenzene sulfonyl guanidine was recrystallized from
hot water.
5 parts (0.024 mol) of p-nitrobenzene sulfonyl guanidine was dissolved in 50
parts of boiling 95% alcohol and to the solution was added 0.5 part of
concentrated hydrochloric acid. The solution was heated to reflux and 6 parts
of iron dust was added. The suspension was refluxed for 3 hours, made basic
with potassium carbonate, and filtered hot. The alcohol was evaporated off
and the p-aminobenzene sulfonyl guanidine recrystallized from boiling water
with the addition of decolorizing charcoal.
brand name
Aseptil-guanidina;Coliseptale;Devaguanil;Dirkan;Emerin;Ente-rivo simplex;Granidan;Guamide;Guanicil;Guanimycin;Guanowept;Guasept;Inorgan;Intestovet;Ordenol;Orgaguanidon;Resulfon;Ruocil;Sgd;S-guanidan;S-guanidine;Shigatox;Suganyl;Sulfacarbon;Sulfentidine;Sulfogua;Tetrawest;Trisulvet.
Therapeutic Function
Antimicrobial
World Health Organization (WHO)
Sulfaguanidine, a sulfonamide anti-infective agent, was introduced in 1941 for the treatment of bacterial infections. The importance of sulfonamides has subsequently decreased as a result of increasing bacterial resistance and their replacement by antibiotics which are generally more active and less toxic. The sulfonamides are known to cause serious adverse effects such as renal toxicity sometimes fatal exfoliative dermatitis and erythema multiforma and dangerous adverse reactions affecting blood formation such as agranulocytosis and haemolytic or aplastic anaemia. Although sulfaguanidine, which is poorly absorbed from the gastrointestinal tract, is no longer recommended in some countries, it continues to be used in others for the treatment of local intestinal infections, including bacterial dysentery, and for preoperative bowel preparation.
Pharmaceutical Applications
1-Sulfanilylguanidine. A poorly absorbed compound, less potent than succinylsulfathiazole but with similar uses. Blood concentrations of 15–40 mg/L have been found after single doses of 1–7 g. Excretion in the urine is rapid.
Safety Profile
Moderately toxic by intraperitoneal route. An experimental teratogen. Other experimental reproductive effects. See also SULFONATES. When heated to decomposition it emits very toxic fumes of SO, and NO,.
Purification Methods
Crystallise the antibacterial from hot water (7mL/g). [Beilstein 14 III 1970, 14 IV 2668.]
Sulfaguanidine Preparation Products And Raw materials
Raw materials
1of2
Preparation Products
| Supplier | Tel | Country | ProdList | Advantage | |
|---|---|---|---|---|---|
| Hebei Weibang Biotechnology Co., Ltd | +8615531157085 | abby@weibangbio.com | China | 8817 | 58 |
| Hebei Mojin Biotechnology Co., Ltd | +86 13288715578 +8613288715578 | sales@hbmojin.com | China | 12837 | 58 |
| Hebei Yanxi Chemical Co., Ltd. | +8617531190177 | peter@yan-xi.com | China | 5858 | 58 |
| Hebei Weibang Biotechnology Co., Ltd | +8617732866630 | bess@weibangbio.com | China | 18194 | 58 |
| shandong perfect biotechnology co.ltd | +86-53169958659; +8618596095638 | sales@sdperfect.com | China | 294 | 58 |
| Shaanxi TNJONE Pharmaceutical Co., Ltd | +8618092446649 | sarah@tnjone.com | China | 1143 | 58 |
| Henan Suikang Pharmaceutical Co.,Ltd. | +86-18239973690 +86-18239973690 | sales@suikangpharm.com | China | 311 | 58 |
| Capot Chemical Co.,Ltd. | +86-（0）57185586718 +86-13336195806 | sales@capot.com | China | 29791 | 60 |
| Henan Tianfu Chemical Co.,Ltd. | +86-0371-55170693 +86-19937530512 | info@tianfuchem.com | China | 21639 | 55 |
| Hubei XinRunde Chemical Co., Ltd. | +8615102730682 | bruce@xrdchem.cn | CHINA | 566 | 55 |
View Lastest Price from Sulfaguanidine manufacturers
| Image | Update time | Product | Price | Min. Order | Purity | Supply Ability | Manufacturer | |
|---|---|---|---|---|---|---|---|---|
 |
2024-10-31 | Sulfaguanidine
57-67-0
|
US $78.00 / g | 99.74% | 10g | TargetMol Chemicals Inc. | ||
 |
2024-10-31 | Sulfaguanidine
57-67-0
|
US $78.00 / g | 99.74% | 10g | TargetMol Chemicals Inc. | ||
 |
2024-10-30 | Sulfaguanidine
57-67-0
|
US $1.00 / KG | 1KG | 99% | 10mt | Hebei Weibang Biotechnology Co., Ltd |
-
- Sulfaguanidine
57-67-0
- US $78.00 / g
- 99.74%
- TargetMol Chemicals Inc.
-
- Sulfaguanidine
57-67-0
- US $78.00 / g
- 99.74%
- TargetMol Chemicals Inc.
-
- Sulfaguanidine
57-67-0
- US $1.00 / KG
- 99%
- Hebei Weibang Biotechnology Co., Ltd