4-Hydroxybenzylamine

4-Hydroxybenzylamine
  • CAS No.:696-60-6
Other grades of this product :
4-Hydroxybenzylamine Basic information
Product Name:4-Hydroxybenzylamine
Synonyms:RARECHEM AL BW 0048;4-HYDROXYBENZYLAMINE[4-(AMINOMETHYL)PHENOL];4-(AMINOMETHYL)PHENOL;4-HYDROXYBENZYLAMINE;4-Hydroxybenzylamine, (4-Hydroxyphenyl)methylamine;4-(aminomethyl)phenol hydrochloride;4-Hydroxybenzylamine monohydrate, 97%;[(4-Hydroxyphenyl)Methyl]aMine
CAS:696-60-6
MF:C7H9NO
MW:123.15
EINECS:
Product Categories:Amines;Aromatics;Anilines, Aromatic Amines and Nitro Compounds;Intermediates
Mol File:696-60-6.mol
4-Hydroxybenzylamine Chemical Properties
Melting point 123-128 °C
Boiling point 262.4±15.0 °C(Predicted)
density 1.141±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
solubility DMSO (Slightly), Water (Slightly, Heated)
pka8.93±0.26(Predicted)
form Powder
color Off-white to pale yellow
InChIKeyRQJDUEKERVZLLU-UHFFFAOYSA-N
CAS DataBase Reference696-60-6(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 34-36/37/38
Safety Statements 26-36/37/39-24/25
RIDADR 2735
WGK Germany 3
Hazard Note Irritant
HazardClass IRRITANT, CORROSIVE
HS Code 29214990
MSDS Information
4-Hydroxybenzylamine Usage And Synthesis
Description4-HOBA is an isomer of the isoketal scavenger 2-HOBA that has reduced efficacy as an isoketal scavenger. Unlike 2-HOBA, 4-HOBA has no effect on hypertension induced by angiotensin II in mice. 4-HOBA has been used as a negative control for the activity of 2-HOBA and related compounds in a mouse model of hypertension.
Chemical Properties4-Hydroxybenzylamine, also known as tyramine and p-hydroxyphenethylamine, is a white or off-white or light green solid. Tyramine, a compound originally isolated from ergot alkaloids and decomposed animal tissues, is an important synthetic drug intermediate.
Uses4-Hydroxybenzylamine (cas# 696-60-6) is a compound useful in organic synthesis.
PreparationSynthesis of 4-Hydroxybenzylamine:Ammonia is passed into 500 ml of ethanol at 10° C. until saturation is reached, 122.1 g=1 mole of p-hydroxybenzaldehyde, 20 g of Raney nickel and 0.1 ml of concentrated sulfuric acid are added and the mixture is stirred in an autoclave for 6 hours at room temperature and under a hydrogen pressure of 100 atmospheres. After releasing the pressure, the catalyst is filtered off and the filtrate is boiled up with active charcoal, filtered and concentrated. The residue is recrystallized from a mixture of ethanol and ether. This gives 104 g (85% of theory), melting point: 104° C.Literature source US04391805
4-Hydroxybenzylamine Preparation Products And Raw materials
Preparation Products4-[2-(DIMETHYLAMINO)ETHOXY]BENZYLAMINE

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