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3-Hydroxybenzylamine

CAS# 73604-31-6

3-Hydroxybenzylamine

Catalog No. BCN1804----Order now to get a substantial discount!

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Quality Control of 3-Hydroxybenzylamine

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Chemical structure

3-Hydroxybenzylamine

3D structure

Chemical Properties of 3-Hydroxybenzylamine

Cas No. 73604-31-6 SDF Download SDF
PubChem ID 735894 Appearance Cryst.
Formula C7H9NO M.Wt 123.15
Type of Compound Alkaloids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 3-(aminomethyl)phenol
SMILES C1=CC(=CC(=C1)O)CN
Standard InChIKey JNZYADHPGVZMQK-UHFFFAOYSA-N
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Source of 3-Hydroxybenzylamine

The herbs of Reseda media

Protocol of 3-Hydroxybenzylamine

Structure Identification
Tetrahedron, 1977, 33(1):489-495.

Photochemical synthesis of 1,2,3,4-tetrahydroisoquinolin-3-ones from N-chloroacetylbenzylamines.[Reference: WebLink]


METHODS AND RESULTS:
When N-chloroacetyl-3-Hydroxybenzylamine (37) in aqueous acetonitrile was irradiated, both ortho and para photocyclizations with reference to the OH group occurred to give 7- and 5-hydroxy-3-oxo-1,2,3,4-tetrahydroisoquinolines (52,53). Similarly, 1-methylisoquinoline derivatives (54,55) were synthesized. N-Chloroacetyl-3,5-dihydroxybenzylamine (39) gave a single photoproduct, 5,7-dihydroxy-3-oxo-1,2,3,4-tetrahydroisoquinoline (56). These photocyclizations were smoothly extended to the synthesis of 1-benzyl, 1-(4′-methoxybenzyl)- and 1-(3′,4′,5′-trimethoxybenzyl)-isoquinoline derivatives (58∼64).

3-Hydroxybenzylamine Dilution Calculator

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3-Hydroxybenzylamine Molarity Calculator

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Preparing Stock Solutions of 3-Hydroxybenzylamine

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 8.1202 mL 40.6009 mL 81.2018 mL 162.4036 mL 203.0045 mL
5 mM 1.624 mL 8.1202 mL 16.2404 mL 32.4807 mL 40.6009 mL
10 mM 0.812 mL 4.0601 mL 8.1202 mL 16.2404 mL 20.3004 mL
50 mM 0.1624 mL 0.812 mL 1.624 mL 3.2481 mL 4.0601 mL
100 mM 0.0812 mL 0.406 mL 0.812 mL 1.624 mL 2.03 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on 3-Hydroxybenzylamine

Determination of catechol-O-methyltransferase activity by high-performance liquid chromatography with electrochemical detection.[Pubmed:6731809]

Anal Biochem. 1984 Feb;137(1):69-73.

A rapid and simple assay for catechol-O-methyltransferase (COMT) activity by high-performance liquid chromatography with electrochemical detection is described. The method is based on the measurement of 3-O- and 4-O-methylated products (3-methoxy-4-hydroxy- and 4-methoxy-3-Hydroxybenzylamine, respectively) of the substrate 3,4-dihydroxybenzylamine. These compounds are determined from the incubation mixture after removal of protein injecting aliquot into the liquid chromatograph. The detection limit is 1 pmol of product. This method is very suitable for screening of COMT activity as well as for determining the meta/para product ratios.

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