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Chemical structure of 1,7-Heptanediol | 629-30-1
CAS: 42823-46-1
SKU: S1600
4-Guanidinobenzoic acid hydrochloride | SKU: S1600
Chemical structure of 1,7-Heptanediol | 629-30-1
Request Quote — S1600

Specifications

AppearanceN/A
Content of ZincN/A
Boiling PointN / A
Melting Point276°C
Vapor PressureN/A
% Volatile by WeightN/A
Solubility in WaterN/A
DensityN/A
pH of Liquid, Typical (10% soln)N/A
Specific Gravity ApproxN/A
OdorN/A
pHN/A
Flash PointN/A
Ignition temperatureN/A
Lower exposure limitN/A
Upper exposure limitN/A
ColorWhite
Formula Weight215.64
Physical FormCrystal-Powder at 20°C
Chemical Name or Material4-Guanidinobenzoic Acid Hydrochloride

Applications

No Application Found

Product Description

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

Safety Information

No Safety Information Available.

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FAQs: 4-Guanidinobenzoic acid hydrochloride

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.