| Identification | More | [Name]
4-Hydroxybenzylamine | [CAS]
696-60-6 | [Synonyms]
4-(AMINOMETHYL)PHENOL
4-HYDROXYBENZYLAMINE
RARECHEM AL BW 0048
4-HYDROXYBENZYLAMINE[4-(AMINOMETHYL)PHENOL]
4-(aminomethyl)phenol hydrochloride | [Molecular Formula]
C7H9NO | [MDL Number]
MFCD00870499 | [Molecular Weight]
123.15 | [MOL File]
696-60-6.mol |
| Chemical Properties | Back Directory | [Melting point ]
123-128 °C | [Boiling point ]
262.4±15.0 °C(Predicted) | [density ]
1.141±0.06 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Inert atmosphere,2-8°C | [solubility ]
DMSO (Slightly), Water (Slightly, Heated) | [form ]
Powder | [pka]
8.93±0.26(Predicted) | [color ]
Off-white to pale yellow | [InChIKey]
RQJDUEKERVZLLU-UHFFFAOYSA-N | [LogP]
0.350 (est) | [CAS DataBase Reference]
696-60-6(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R34:Causes burns. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . | [RIDADR ]
2735 | [WGK Germany ]
3 | [Hazard Note ]
Irritant | [HazardClass ]
IRRITANT, CORROSIVE | [HS Code ]
29214990 |
| Hazard Information | Back Directory | [Description]
4-HOBA is an isomer of the isoketal scavenger 2-HOBA (Item No. 25357) that has reduced efficacy as an isoketal scavenger.1 Unlike 2-HOBA, 4-HOBA has no effect on hypertension induced by angiotensin II (Item No. 17150) in mice.1 4-HOBA has been used as a negative control for the activity of 2-HOBA and related compounds in a mouse model of hypertension.1 | [Chemical Properties]
Light Green Solid | [Uses]
4-Hydroxybenzylamine (cas# 696-60-6) is a compound useful in organic synthesis. | [Definition]
ChEBI: 4-Hydroxybenzylamine is an aromatic amine. | [Preparation]
Synthesis 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 | [target]
GABA Receptor |
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