Welcome to LookChem.com Sign In|Join Free
  • or
Home > Products >  > 

Ampicillin sodium

Related Products

Hot Products

Name

Ampicillin sodium

EINECS 200-708-1
CAS No. 69-52-3 Density N/A
PSA 140.86000 LogP 0.01250
Solubility water: 50 mg/mL, clear, very faintly yellow Melting Point 215 °C (dec.)(lit.)
Formula C16H18N3NaO4S Boiling Point 683.9 °C at 760 mmHg
Molecular Weight 371.392 Flash Point 367.4 °C
Transport Information N/A Appearance White powder
Safety 22-36/37-45 Risk Codes 42/43
Molecular Structure Molecular Structure of 69-52-3 (Ampicillin sodium) Hazard Symbols IrritantXi
Synonyms

Alpen-N;Amcill-S;Ampicillin natrium;Ampicillin sodium;Ampicillin sodium salt;Binotal sodium;Citteral;D(-)-alpha-Aminobenzylpenicillin sodium salt;Domicillin;Monosodium (2S,5R,6R)-6-((R)-2-Amino-2-phenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylate;

Article Data 4

Ampicillin sodium Synthetic route

71780-15-9

N-(1-methyl-2-ethoxycarbonylvinyl)ampicillin sodium

69-52-3

ampicillin sodium

Conditions
ConditionsYield
With water at 25℃; Rate constant; hydrolysis at pH 7.4;
69-52-3

ampicillin sodium

141-97-9

ethyl acetoacetate

71780-15-9

N-(1-methyl-2-ethoxycarbonylvinyl)ampicillin sodium

Conditions
ConditionsYield
In isopropyl alcohol at 25℃; for 3h;75%

Ampicillin sodium Consensus Reports

IARC Cancer Review: Group 3 IMEMDT    IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man . 50 ,1990,p. 153.(World Health Organization, Internation Agency for Research on Cancer,Lyon, France.: ) (Single copies can be ordered from WHO Publications Centre U.S.A., 49 Sheridan Avenue, Albany, NY 12210) ; Animal Limited Evidence IMEMDT    IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man . 50 ,1990,p. 153.(World Health Organization, Internation Agency for Research on Cancer,Lyon, France.: ) (Single copies can be ordered from WHO Publications Centre U.S.A., 49 Sheridan Avenue, Albany, NY 12210) ; Human Inadequate Evidence IMEMDT    IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man . 50 ,1990,p. 153.(World Health Organization, Internation Agency for Research on Cancer,Lyon, France.: ) (Single copies can be ordered from WHO Publications Centre U.S.A., 49 Sheridan Avenue, Albany, NY 12210) .

Ampicillin sodium Specification

The Ampicillin sodium, with the CAS registry number 69-52-3 and EINECS registry number 200-708-1, has the systematic name of sodium (2S,5R,6R)-6-{[(2R)-2-amino-2-phenylacetyl]amino}-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate. It is a kind of white powder, and the molecular formula of this chemical is C16H18N3NaO4S. As a semi-synthetic derivative of penicillin, it functions as an orally active broad-spectrum antibiotic. And it should be stored at 2-8°C.

The physical properties of Ampicillin sodium are as following: (1)ACD/LogP: 1.35; (2)# of Rule of 5 Violations: 0; (3)#H bond acceptors: 7; (4)#H bond donors: 4; (5)#Freely Rotating Bonds: 5; (6)Polar Surface Area: 106.46 Å2; (7)Flash Point: 367.4 °C; (8)Enthalpy of Vaporization: 105.36 kJ/mol; (9)Boiling Point: 683.9 °C at 760 mmHg; (10)Vapour Pressure: 1.21E-19 mmHg at 25°C.

Synthetic method and uses of Ampicillin sodium: It can be obtained by the salifing of penbritin: Add penbritin to the water, and adjust the pH to 9 by adding sodium hydroxide solution. Then you can get the product after a series of decoloration, filtration and drying. And because of its tericidal action, it is often used in the molecular biology and also used for tissue culture(to prevent microbial contamination).

You should be cautious while dealing with this chemical. It may cause sensitization by inhalation and skin contact. Therefore, you had better take the following instructions: Wear suitable protective clothing and gloves, and in case of accident or if you feel unwell, seek medical advice immediately (show label where possible); Do not breathe dust.

You can still convert the following datas into molecular structure:
(1)SMILES: [Na+].O=C([O-])[C@@H]2N3C(=O)[C@@H](NC(=O)[C@@H](c1ccccc1)N)[C@H]3SC2(C)C
(2)InChI: InChI=1/C16H19N3O4S.Na/c1-16(2)11(15(22)23)19-13(21)10(14(19)24-16)18-12(20)9(17)8-6-4-3-5-7-8;/h3-7,9-11,14H,17H2,1-2H3,(H,18,20)(H,22,23);/q;+1/p-1/t9-,10-,11+,14-;/m1./s1
(3)InChIKey: KLOHDWPABZXLGI-IANBRGBNBB

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intraperitoneal 5700mg/kg (5700mg/kg)   Toxicology and Applied Pharmacology. Vol. 18, Pg. 185, 1971.
mouse LD50 oral > 5314mg/kg (5314mg/kg)   British Journal of Pharmacology and Chemotherapy. Vol. 18, Pg. 356, 1962.
mouse LD50 subcutaneous > 5314mg/kg (5314mg/kg)   British Journal of Pharmacology and Chemotherapy. Vol. 18, Pg. 356, 1962.
mouse LDLo intravenous 2657mg/kg (2657mg/kg) BEHAVIORAL: TREMOR

BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD

LUNGS, THORAX, OR RESPIRATION: RESPIRATORY DEPRESSION
British Journal of Pharmacology and Chemotherapy. Vol. 18, Pg. 356, 1962.
rat LD50 intraperitoneal 7400mg/kg (7400mg/kg)   Toxicology and Applied Pharmacology. Vol. 18, Pg. 185, 1971.
rat LD50 oral > 5314mg/kg (5314mg/kg)   British Journal of Pharmacology and Chemotherapy. Vol. 18, Pg. 356, 1962.
rat LD50 subcutaneous > 5314mg/kg (5314mg/kg)   British Journal of Pharmacology and Chemotherapy. Vol. 18, Pg. 356, 1962.
women TDLo oral 100mg/kg/5D (100mg/kg) GASTROINTESTINAL: "HYPERMOTILITY, DIARRHEA"

GASTROINTESTINAL: OTHER CHANGES
Lancet. Vol. 2, Pg. 707, 1978.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 69-52-3