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alpha-[(2-pyridylamino)methyl]benzyl alcohol monohydrochloride

Product Name
alpha-[(2-pyridylamino)methyl]benzyl alcohol monohydrochloride
CAS No.
326-43-2
Chemical Name
alpha-[(2-pyridylamino)methyl]benzyl alcohol monohydrochloride
Synonyms
Vazalmin;Firmalgil;Phenyramidol HCl;FENYRAMIDOLHYDROCHLORIDE;1-Phenyl-2-(pyridin-2-ylamino)ethanol hydrochloride;alpha-[(2-pyridylamino)methyl]benzyl alcohol monohydrochloride;Benzenemethanol, a-[(2-pyridinylamino)methyl]-,hydrochloride (1:1)
CBNumber
CB1906929
Molecular Formula
C13H15ClN2O
Formula Weight
250.724
MOL File
326-43-2.mol
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alpha-[(2-pyridylamino)methyl]benzyl alcohol monohydrochloride Property

Melting point:
140-142°
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Safety

Toxicity
LD50 oral in mouse: 2425mg/kg
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
API0016333
Product name
PHENYRAMIDOL HYDROCHLORIDE
Purity
95.00%
Packaging
5MG
Price
$496.22
Updated
2021/12/16
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alpha-[(2-pyridylamino)methyl]benzyl alcohol monohydrochloride Chemical Properties,Usage,Production

Originator

Analexin, Mallinckrodt Inc., US ,1960

Uses

Analgesic; relaxant (skeletal muscle).

Manufacturing Process

A mixture containing 188 g (0.20 mol) of 2-arninopyridine, 0.55 g of lithium amide and 75 cc of anhydrous toluene was refluxed for 1.5 hours. Styrene oxide (12.0 g = 0.10 mol) was then added to the reaction mixture with stirring over a period of ten minutes. The reaction mixture was stirred and refluxed for an additional 3.5 hours. A crystalline precipitate was formed during the reaction which was removed by filtration, MP 170°C to 171°C. 1.5 g. The filtrate was concentrated to dryness and a dark residue remained which was crystallized from anhydrous ether; yield 6.0 g. Upon recrystallization of the crude solid from 30 cc of isopropyl alcohol, 2.0 g of a light yellow solid was isolated; MP 170° to 171°C.

Therapeutic Function

Analgesic, Muscle relaxant

alpha-[(2-pyridylamino)methyl]benzyl alcohol monohydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

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alpha-[(2-pyridylamino)methyl]benzyl alcohol monohydrochloride Suppliers

TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
19892
Advantage
58
Alfa Chemistry
Tel
+1-5166625404
Fax
1-516-927-0118
Email
Info@alfa-chemistry.com
Country
United States
ProdList
21317
Advantage
58

326-43-2, alpha-[(2-pyridylamino)methyl]benzyl alcohol monohydrochloride Related Search:


  • alpha-[(2-pyridylamino)methyl]benzyl alcohol monohydrochloride
  • FENYRAMIDOLHYDROCHLORIDE
  • Firmalgil
  • Phenyramidol HCl
  • Vazalmin
  • 1-Phenyl-2-(pyridin-2-ylamino)ethanol hydrochloride
  • Benzenemethanol, a-[(2-pyridinylamino)methyl]-,hydrochloride (1:1)
  • 326-43-2