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Penicillin G procaine salt monohydrate - ≥98%, high purity , CAS No.6130-64-9

COA

Grade & Purity:

≥98%

Cas Number: 6130-64-9
Molecular Weight: 588.72
PubChem CID: 22502
PubChem SID: 488182762

In stock

Item Number

P274715

Grouped product items
SKU	Size	Availability	Price
P274715-25mg	25mg	2	$296.90
P274715-100mg	100mg	2	$893.90
P274715-250mg	250mg	2	$1,580.90

Combination of Penicillin G and Procaine

View related series

Antibiotic (1629) Bacterial (3013)

Basic Description

Synonyms	F82417 \| Ampin-penicillin \| Parencillin \| Penicillin G procaine [USP] \| Kabipenin \| Penicillin G procaine (hydrate) \| NOVOCAINE PENICILLIN \| Penicillin G procaine (USP) \| Abbocillin-DC \| PROCAINI BENZYLPENICILLINUM [WHO-IP LATIN] \| Aquasuspen \| s5515 \| Aq
Specifications & Purity	≥98%
Biochemical and Physiological Mechanisms	Antibiotic. Combination of Penicillin G and Procaine. Antibacterial and antimicrobial agent. Active in vivo.
Storage Temp	Store at -20°C
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Note	Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description	Penicillin G Procaine(PGP), a β-lactam antibiotic, is a crystalline complex produced by chemically combining penicillin G with procaine.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Class Carboxylic acids and derivatives
    - Subclass Amino acids, peptides, and analogues
      - Level5 Peptides
        Level6 Dipeptides

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Class	Carboxylic acids and derivatives
Subclass	Amino acids, peptides, and analogues
Intermediate Tree Nodes	Peptides
Direct Parent	Dipeptides
Alternative Parents	Penicillins N-acyl-alpha amino acids and derivatives Aminobenzoic acids and derivatives Benzoic acid esters Phenylacetamides Aniline and substituted anilines Benzoyl derivatives Tertiary carboxylic acid amides Thiazolidines Carboxylic acid esters Trialkylamines Azetidines Secondary carboxylic acid amides Monocarboxylic acids and derivatives Dialkylthioethers Carboxylic acids Thiohemiaminal derivatives Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Primary amines
Molecular Framework	Not available
Substituents	Alpha-dipeptide - Penicillin - N-acyl-alpha amino acid or derivatives - Alpha-amino acid or derivatives - Aminobenzoic acid or derivatives - Benzoate ester - Phenylacetamide - Benzoic acid or derivatives - Benzoyl - Aniline or substituted anilines - Penam - Monocyclic benzene moiety - Benzenoid - Thiazolidine - Tertiary carboxylic acid amide - Beta-lactam - Tertiary aliphatic amine - Amino acid or derivatives - Tertiary amine - Secondary carboxylic acid amide - Azetidine - Carboxamide group - Carboxylic acid ester - Lactam - Hemithioaminal - Thioether - Dialkylthioether - Organoheterocyclic compound - Carboxylic acid - Monocarboxylic acid or derivatives - Azacycle - Amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Primary amine - Organic nitrogen compound - Aromatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as dipeptides. These are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

Pubchem Sid	488182762
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488182762
IUPAC Name	2-(diethylamino)ethyl 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
INCHI	InChI=1S/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
InChIKey	KZDCMKVLEYCGQX-UDPGNSCCSA-N
Smiles	CCN(CC)CCOC(=O)C1=CC=C(C=C1)N.CC1(C(N2C(S1)C(C2=O)NC(=O)CC3=CC=CC=C3)C(=O)O)C.O
Isomeric SMILES	CCN(CC)CCOC(=O)C1=CC=C(C=C1)N.CC1([C@@H](N2[C@H](S1)[C@@H](C2=O)NC(=O)CC3=CC=CC=C3)C(=O)O)C.O
Alternate CAS	54-35-3
PubChem CID	22502
Molecular Weight	588.72

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

7 results found

Lot Number	Certificate Type	Date	Item
C2504035	Certificate of Analysis	Mar 06, 2025	P274715
B2320501	Certificate of Analysis	Mar 07, 2024	P274715
B2320447	Certificate of Analysis	Feb 01, 2024	P274715
B2320528	Certificate of Analysis	Feb 01, 2024	P274715
B2320488	Certificate of Analysis	Dec 20, 2023	P274715
B2320448	Certificate of Analysis	Dec 20, 2023	P274715
B2320446	Certificate of Analysis	Dec 20, 2023	P274715

Chemical and Physical Properties

Solubility	Soluble in water
Molecular Weight	588.700 g/mol
XLogP3
Hydrogen Bond Donor Count	4
Hydrogen Bond Acceptor Count	10
Rotatable Bond Count	11
Exact Mass	588.262 Da
Monoisotopic Mass	588.262 Da
Topological Polar Surface Area	169.000 Å²
Heavy Atom Count	41
Formal Charge	0
Complexity	752.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	3
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	3

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