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2-Hydroxybenzylamine

CAS No.
932-30-9
Chemical Name:
2-Hydroxybenzylamine
Synonyms
2-(Aminomethyl)phenol;2-HydroxybenzyL;Phenol, 2-(aminomethyl)-;2-HOBA;NSC 127870;Salicylamine;α-AMino-o-cresol;o-HydroxybenzylaMine;2-Hydroxybenzylamine;2-Hydroxybenzylamine,98%
CBNumber:
CB4197977
Molecular Formula:
C7H9NO
Molecular Weight:
123.15
MDL Number:
MFCD03426060
MOL File:
932-30-9.mol
MSDS File:
SDS
Last updated:2023-09-21 18:25:44

2-Hydroxybenzylamine Properties

Melting point 127 °C
Boiling point 245.0±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 Chloroform (Slightly), Methanol (Very Slightly, Heated)
form Solid
pka 8.63±0.35(Predicted)
color Beige to Brown
FDA UNII 696R5N4NRM

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-37/39
WGK Germany  3
HazardClass  IRRITANT
HS Code  29222990
NFPA 704
0
2 0

2-Hydroxybenzylamine price More Price(31)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich CDS008020 2-(aminomethyl)phenol Aldrich 932-30-9 250mg $209 2024-03-01 Buy
Cayman Chemical 25357 2-HOBA ≥98% 932-30-9 250mg $44 2024-03-01 Buy
Cayman Chemical 25357 2-HOBA ≥98% 932-30-9 500mg $84 2024-03-01 Buy
Cayman Chemical 25357 2-HOBA ≥98% 932-30-9 1g $155 2024-03-01 Buy
Cayman Chemical 25357 2-HOBA ≥98% 932-30-9 5g $680 2024-03-01 Buy
Product number Packaging Price Buy
CDS008020 250mg $209 Buy
25357 250mg $44 Buy
25357 500mg $84 Buy
25357 1g $155 Buy
25357 5g $680 Buy

2-Hydroxybenzylamine Chemical Properties,Uses,Production

Description

2-Hydroxybenzylamine (2-HOBA), also known as salicylamide, is a potent γKA scavenger that scavenges γKAs 980-fold faster than the formation of γKA protein adducts and therefore protects cells from the deleterious effects of γKA adducts. 2-HOBA is currently being developed as a nutritional supplement to help protect against the development of conditions associated with dicarbonyl electrophile formation, such as the cognitive decline observed with Mild Cognitive Impairment or Alzheimer's disease.

Chemical Properties

white to light yellow crystal powder.

Uses

2-Hydroxybenzylamine is a potent γ-ketoaldehyde scavenger that has been shown to protects cardiac sodium channel (NaV1.5) from oxidant-induced inactivation.

Production Methods

A simplified method for extracting 2-hydroxybenzylamine from buckwheat is as follows:
1. Dry the roots, stems, and seeds of buckwheat separately. Grind them into a powder using liquid nitrogen.
2. Mix the powder with deionized water and adjust the pH of the solution to 5.0. Add an enzyme mixture consisting of cellulase and pectinase, with a weight ratio of 2:1 to the powder. Perform enzymatic hydrolysis at a temperature of 25°C for 40 minutes. Filter the mixture after hydrolysis.
3. Mix the filter residue obtained in step 2 with 95% ethanol using a solid-liquid ratio of 1g:10mL. Perform ultrasonic extraction at an ultrasound power density of 100W/cm2, ultrasound frequency of 30kHz, extraction temperature of 20°C, and extraction time of 30 minutes. Repeat the extraction process three times, filter the extracts, and combine them.
4. Concentrate the supernatant obtained in step 3 under reduced pressure to obtain a Chemicalbook extract. Add a 3 wt% sodium hydroxide solution to dissolve the extract. Filter the solution to obtain the filtrate.
5. Adjust the filtrate obtained in step 4 to pH 3 using hydrochloric acid, resulting in an adjusted solution. Pass the adjusted solution through an NDA-150 resin column at a temperature of 20°C and a flow rate of 10 BV/h until saturated adsorption is achieved.
6. After reaching saturated adsorption, elute the filtrate obtained in step 4 with an 8 wt% sodium hydroxide solution at 50°C and a flow rate of 2 BV/h. Collect twice the volume of the column volume. Then, elute the filtrate obtained in step 5 with a 3 wt% sodium hydroxide solution at 50°C and a flow rate of 2 BV/h. Collect once the volume of the column volume. Lastly, elute the filtrate obtained in step 5 with water at 60°C and a flow rate of 3 BV/h. Collect once the volume of the column volume. Combine the three eluents.
7. Concentrate the combined eluents under reduced pressure and recrystallize them using edible alcohol. Separate the crystals to obtain 2-hydroxybenzylamine.

Synthesis Reference(s)

Tetrahedron, 48, p. 4301, 1992 DOI: 10.1016/S0040-4020(01)80441-5

611-20-1
932-30-9
Synthesis of 2-Hydroxybenzylamine from 2-Cyanophenol
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View Lastest Price from 2-Hydroxybenzylamine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2-Hydroxybenzylamine pictures 2023-07-27 2-Hydroxybenzylamine
932-30-9
US $1.50 / g 1g 99.0% Min 100 Tons Shaanxi Didu New Materials Co. Ltd
2-Hydroxybenzylamine pictures 2023-03-06 2-Hydroxybenzylamine
932-30-9
US $9.00 / KG 1KG 99.8% 100tons Hebei Guanlang Biotechnology Co,.LTD
2-Hydroxybenzylamine pictures 2022-02-23 2-Hydroxybenzylamine
932-30-9
US $0.00 / KG 1KG 97.2% 100 tons Honest Joy Holdings Limited
2-(3-CHLOROPHENOXY)MALONDIALDEHYDE 2-Hydroxybenzylamine 2-Hydroxybenzylamine, (2-Hydroxyphenyl)methylamine 2-HydroxybenzylaMine, 98% 1GR 2-HydroxybenzeneMethanaMine NSC 127870 o-HydroxybenzylaMine α-AMino-o-cresol Salicylamine 2-Hydroxybenzylamine,98% 2-HOBA 2-Hydroxybenzylamine USP/EP/BP Phenol, 2-(aminomethyl)- 2-(Aminomethyl)phenol 2-HydroxybenzyL 2-HYDROXYBENZYLAMINE[2-(AMINOMETHYL)PHENOL] antioxidant,IsoLGs,inhibit,Inhibitor,atherosclerosis,scavenger,oxidative stress,atrial fibrillation,arrhythmias,o-Hydroxybenzylamine,FH model,inflammation,radical,Reactive Oxygen Species,2-HOBA,2 Hydroxybenzylamine,2Hydroxybenzylamine 932-30-9 Phenyls & Phenyl-Het Anilines, Aromatic Amines and Nitro Compounds Amines Aromatics Intermediates & Fine Chemicals Pharmaceuticals Aminomethyl's Phenyls & Phenyl-Het Amine