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Procaine penicilline G hydrate

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Name

Procaine penicilline G hydrate

EINECS 612-112-2
CAS No. 6130-64-9 Density 1.255-1.256
PSA 201.30000 LogP 3.10500
Solubility N/A Melting Point 106-110° (with decompn)
Formula C16H18N2O4S.C13H20N2O2.H2O Boiling Point 663.3 °C at 760 mmHg
Molecular Weight 588.72 Flash Point 355 °C
Transport Information N/A Appearance N/A
Safety 36 Risk Codes 42/43
Molecular Structure Molecular Structure of 6130-64-9 (Procaine penicilline G hydrate) Hazard Symbols HarmfulXn
Synonyms

Duracillin (TN);Penicillin G procaine (USP);Duracillin;PENICILLIN G;Penicillin g procaine & dihydrostreptomycin sulphate suspension for inj.;

 

Procaine penicilline G hydrate Specification

The IUPAC name of Procaine penicilline G hydrate is 2-diethylaminoethyl 4-aminobenzoate; (2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid; hydrate. With the CAS registry number 6130-64-9, it is also named as 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-((phenylacetyl)amino)-, (2S-2alpha,5alpha,6beta))-, compd. with 2-(diethylamino)ethyl 4-aminobenzoate (1:1) monohydrate; Abbocillin. The classification codes are Anti-Bacterial Agents, Anti-Infective Agents, Antibacterial, Drug / Therapeutic Agent and Human Data.

The other characteristics of this product can be summarized as: (1)ACD/LogP: 1.67; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -1.31; (4)ACD/LogD (pH 7.4): -2.06; (5)ACD/BCF (pH 5.5): 1; (6)ACD/BCF (pH 7.4): 1; (7)ACD/KOC (pH 5.5): 1; (8)ACD/KOC (pH 7.4): 1; (9)#H bond acceptors: 6; (10)#H bond donors: 2; (11)#Freely Rotating Bonds: 4; (12)Enthalpy of Vaporization: 102.51 kJ/mol; (13)Vapour Pressure: 1.69E-18 mmHg at 25°C; (14)Rotatable Bond Count: 11; (15)Tautomer Count: 12; (16)Exact Mass: 588.26177; (17)MonoIsotopic Mass: 588.26177; (18)Topological Polar Surface Area: 169; (19)Heavy Atom Count: 41; (20)Complexity: 752.

When you are using this chemical, please be cautious about it as the following. It may cause sensitization by inhalation and skin contact. If you want to contact this product, you must wear suitable protective clothing.

People can use the following data to convert to the molecule structure.
1. SMILES: O=C(O)[C@@H]2N3C(=O)[C@@H](NC(=O)Cc1ccccc1)[C@H]3SC2(C)C.O=C(OCCN(CC)CC)c1ccc(N)cc1.O;
2. InChI: InChI=1/C16H18N2O4S.C13H20N2O2.H2O/c1-16(2)12(15(21)22)18-13(20)11(14(18)23-16)17-10(19)8-9-6-4-3-5-7-9;1-3-15(4-2)9-10-17-13(16)11-5-7-12(14)8-6-11;/h3-7,11-12,14H,8H2,1-2H3,(H,17,19)(H,21,22);5-8H,3-4,9-10,14H2,1-2H3;1H2/t11-,12+,14-;;/m1../s1.

The following is the toxicity data which has been tested.

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
dog LDLo subcutaneous > 545mg/kg (545mg/kg)   Antibiotics and Chemotherapy Vol. 3, Pg. 421, 1953.
man TDLo intramuscular 4mg/kg (4mg/kg) KIDNEY, URETER, AND BLADDER: INTERSTITIAL NEPHRITIS

SKIN AND APPENDAGES (SKIN): "DERMATITIS, ALLERGIC: AFTER SYSTEMIC EXPOSURE"
JAMA, Journal of the American Medical Association. Vol. 147, Pg. 1139, 1951.
mouse LD50 intramuscular > 1gm/kg (1000mg/kg)   Arzneimittel-Forschung. Drug Research. Vol. 9, Pg. 31, 1959.
mouse LD50 intraperitoneal 146mg/kg (146mg/kg)   Research Progress in Organic-Biological and Medicinal Chemistry. Vol. 2, Pg. 306, 1970.
mouse LD50 intravenous 119mg/kg (119mg/kg)   Arzneimittel-Forschung. Drug Research. Vol. 9, Pg. 31, 1959.
mouse LD50 oral > 2gm/kg (2000mg/kg)   Antibiotics Annual. Vol. 2, Pg. 133, 1954/1955.
mouse LD50 subcutaneous 2300mg/kg (2300mg/kg)   Arzneimittel-Forschung. Drug Research. Vol. 1, Pg. 28, 1951.
rabbit LD50 intravenous 70mg/kg (70mg/kg)   Antibiotics and Chemotherapy Vol. 5, Pg. 152, 1955.
rat LD50 intravenous 97mg/kg (97mg/kg)   Antibiotics and Chemotherapy Vol. 5, Pg. 152, 1955.
rat LD50 subcutaneous > 6gm/kg (6000mg/kg)   Antibiotics and Chemotherapy Vol. 5, Pg. 152, 1955.

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