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6-AMINOPENICILLANIC ACID | ||
PRODUCT IDENTIFICATION |
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CAS NO. | 551-16-6 |
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EINECS NO. | 208-993-4 | |
FORMULA | C8H12N2O3S | |
MOL WT. | 216.25 | |
H.S. CODE |
2941.10 | |
TOXICITY |
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SYNONYMS | 6-APA; (+)-6-Aminopenicillanic acid; | |
4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-amino-3,3-dimethyl-7- oxo-, [2S-(2alpha,5alpha,6beta)]-; (2S,5R,6R)-6-Amino-3,3-dimethyl-7-oxo-4- thia-1-azabicyclo[3.2.0]heptane-2- carboxylic acid; Acido 6-aminopenicillanico (Italian); 6-Amino-3,3-dimethyl-7-oxo-4-thia-1 -azabicyclo [3.2.0]heptane-2- carboxylic acid; | ||
CLASSIFICATION |
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PHYSICAL AND CHEMICAL PROPERTIES |
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PHYSICAL STATE | white powder | |
MELTING POINT | 198 - 200 C | |
BOILING POINT | > 200 C(Decomposes) | |
SPECIFIC GRAVITY |
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SOLUBILITY IN WATER | ||
pH | ||
VAPOR DENSITY |
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AUTOIGNITION |
> 250 C | |
NFPA RATINGS |
Health: 1; Flammability: 0; Reactivity: 0 | |
REFRACTIVE INDEX |
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FLASH POINT |
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STABILITY |
Stable under ordinary conditions |
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APPLICATIONS |
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6-Aminopenicillanic acid is the active core body of all penicillins substituted at the 6-amino position resulting in a variety of antibacterial and pharmacologic characteristics. It is a non-hygroscopic crystal that decompose at 209 C; | ||
SALES SPECIFICATION | ||
APPEARANCE |
white to off white free flowing crystalline powder |
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IDENTIFICATION |
Complies |
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OPTICAL ROTATION |
+260° ~ +280° |
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ASSAY |
98.0 - 101.0 % |
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PENICILLIN G |
0.6 % max |
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PHENYLACETIC ACID |
0.6 % max |
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SULPHATED ASH |
0.5% max |
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WATER |
0.3% max |
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pH |
3.5 - 5.5 |
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N,N-DIMETHYLANILINE |
Absent |
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TRANSPORTATION | ||
PACKING |
25kgs
in Bag
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HAZARD CLASS | Not regulated | |
UN NO. | ||
OTHER INFORMATION | ||
Hazard Symbols: n/a, Risk Phrases: n/a, Safety Phrases: 24/25 | ||
GENERAL DESCRIPTION OF PENICILLIN |
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· Penicillin: Any of a large group of broad-spectrum antibiotic drugs derived
directly or indirectly from molds of the genus Penicillium and other
soil-inhabiting fungi grown on special culture media, which exert a
bacteriocidal as well as a bacteriostatic effect on susceptible bacteria during
their growth stage by the inhibition of biosynthesis of their cell wall
mucopeptide. Penicillin, beta-lactam antibiotics, possess a four-ring
beta-lactam structure shares a nitrogen and a carbon atom with fused a
five-membered thiazolidine ring. These antibiotics have low toxicity for the
host but effective against most gram-positive bacteria including pathogens
(streptococci, staphylococci, pneumococci); clostridia; some gram-negative
gonococci; some spirochetes (Treponema pallidum and T. pertenue); and some
fungi. Certain strains of some target species, e.g., staphylococci, secrete the
enzyme penicillinase, which inactivates penicillin and confers resistance to the
antibiotic.
· Penicillic acid [CAS RN: 90-65-3]: an antibiotic substance produced by several species of Penicillium and Aspergillus; a white solid soluble in water; melting point 83 - 84 C; antibiotic and mycotoxin induceing DNA single-strand breaks, toxic to animal tissues also, causing nephrotoxicity and other damage. · Penicillin G [also called benzylpenicillin, CAS RN: 61-33-6]: the first and the most widely used penicillin compound for medicinal use. It is used in the form of its stable salts (benzathine, potassium, procaine, and sodium) to treat principally the infections due to penicillin-susceptible gram-positive bacteria, gram-negative cocci, Treponema pallidum, and Actinomyces israelii. · Penicillin G Benzathine [CAS RN: 41372-02-5]: the benzathine salt of penicillin G; having a long-sustained action, administered orally, intramuscularly. Chemically designation is (2S,5R,6R)- 3,3-Dimethyl-7-oxo-6-(2-phenylacetamido)-4-thia-1-azabicyclo [3.2.0] heptane-2-carboxylic acid with N,N' -Dibenzylethylenediamine (2:1). It is a white crystalline powder; slightly soluble in water and sparingly soluble in alcohol. · Penicillin G Potassium [CAS RN: 113-98-4]: the potassium salt of penicillin G; administered orally and by intravenously. It is a white crystalline powder; odorless, moderately hygroscopic; soluble in water. · Penicillin G Procaine [CAS RN: 6130-64-9]: the procaine salt of penicillin G; having a long-sustained action, administered intramuscularly. Chemically designation is (2S,5R,6R)- 3,3-Dimethyl-7-oxo-6-(2-phenylacetamido)-4-thia-1-azabicyclo [3.2.0] heptane-2-carboxylic acid with 2-(Diethylamino)ethyl p-aminobenzoate (1:1). It is a white crystalline powder; slightly soluble in water. · Penicillin G sodium [CAS RN: 69-57-8]: the sodium salt of penicillin G having a potency of 1500–1750 U per mg; administered intramuscularly and intravenously. · Penicillin N (also called adicillin, CAS RN: 525-94-0]: a cephalosporin that is more active against gram-negative organisms than penicillin G and is highly active against Neisseria; has been used in the treatment of typhoid fever and gonorrhea. · Penicillin O: similar to penicillin G in antibiotic action but produced by adding a precursor to the culture medium; penicillin O and its potassium and sodium salts are hypoallergenic. · Penicillin V: [CAS RN: 87-08-1] a semisynthetic penicillin prepared from cultures of the mold Penicillium in the presence of 2-phenoxyethanol with an autolysate of yeast as the source of nitrogen; a white, crystalline powder, soluble in alcohol and acetone; resists destruction by high humidity (gastric juice), thus orally effective. · Penicillin V Benzathine [CAS RN: 63690-57-3] : the benzathine salt of penicillin V, administered orally. Chemical designation is [2S-(2a,5a,6b)]-3,3 -dimethyl-7-oxo-6-[(phenoxyacetyl)amino]-4- thia-1- azabicyclo[3.2.0] heptane-2-carboxylic acid with N,N' -Dibenzylethylenediamine (2:1). · Penicillin V Potassium [CAS RN: 132-98-9]: the potassium salt of penicillin V, administered orally. Chemical designation is [2S-(2a,5a,6b)]-3,3 -dimethyl-7-oxo-6-[(phenoxyacetyl)amino]-4- thia-1- azabicyclo[3.2.0] heptane-2-carboxylic acid, monopotassium salt. |
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PRICE INFORMATION | ||
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