| 3084875 |
Synonym: 4-guanidinobenzoic acid hydrochloride, n-4-carboxyphenyl guanidine hydrochloride, 4-guanidinobenzoic acid hcl, 4-guanidino benzoic acid hydrochloride, 4-amidinoamino benzoic acid, chloride, pubchem14981, pubchem14993, acmc-1an3m, ksc494a0j, 4-guanidino-benzoic acid-hcl salt
| Appearance | N/A |
| Content of Zinc | N/A |
| Boiling Point | N / A |
| Melting Point | 276°C |
| Vapor Pressure | N/A |
| % Volatile by Weight | N/A |
| Solubility in Water | N/A |
| Density | N/A |
| pH of Liquid, Typical (10% soln) | N/A |
| Specific Gravity Approx | N/A |
| Odor | N/A |
| pH | N/A |
| Flash Point | N/A |
| Ignition temperature | N/A |
| Lower exposure limit | N/A |
| Upper exposure limit | N/A |
| Color | White |
| Formula Weight | 215.64 |
| Physical Form | Crystal-Powder at 20°C |
| Chemical Name or Material | 4-Guanidinobenzoic Acid Hydrochloride |
Classification of the substance or mixture
GHS Label elements, including precautionary statements
Hazards not otherwise classified (HNOC) or not covered by GHS
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS). For the full text of the H-Statements mentioned in this Section, see Section 16.
Signal word :
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4-Guanidinobenzoic acid hydrochloride is a crystalline compound derived from guanidinobenzoic acid. It is used in chemical synthesis and biochemical research due to its reactive guanidine group and hydrochloride stability.
4-Guanidinobenzoic acid is the parent compound, while 4-Guanidinobenzoic acid hydrochloride is its salt form. The hydrochloride variant offers enhanced solubility and stability, making it more suitable for laboratory applications.
Key guanidinobenzoic acid hydrochloride properties include high solubility in water, stability under standard storage conditions, and strong basicity due to the guanidine group. It also acts as an effective reagent in biochemical research.
4-Guanidinobenzoic acid hydrochloride is commonly used in peptide synthesis, enzyme inhibition studies, and pharmaceutical research. It’s favored for its reactivity and compatibility with biological systems.
Researchers prefer 4-Guanidinobenzoic acid hydrochloride because it combines the chemical activity of guanidinobenzoic acid with the handling ease of a stable, water-soluble hydrochloride salt.
