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65-28-1

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65-28-1 Usage

Chemical Properties

Crystalline Solid

Uses

Different sources of media describe the Uses of 65-28-1 differently. You can refer to the following data:
1. Phentolamine Mesylate is a nonselective alpha-adrenergic antagonist with IC50 of 0.1 μM
2. Phentolamine Methanesulfonate Salt is an adrenergic blocking agent. An antihypertensive. Used for the treatment of pheochromocytoma.
3. As an adrenergic blocking agent and an antihypertensive, Phentolamine mesilate can be used for the treatment of pheochromocytoma.

General Description

Phentolamine Mesylate belongs to the class of alpha adrenergic antagonist drugs. It is used in the treatment of pheochromocytoma-related hypertension, erectile dysfunction and in the diagnosis of pheochromocytoma and norepinephrine-related dermal necrosis.Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.

Biochem/physiol Actions

α-Adrenergic receptor antagonist; peripheral vasodilator.

Clinical Use

Alpha-adrenoceptor blocker: Hypertensive crisis

Safety Profile

Poison by intravenous and subcutaneous routes. Experimental reproductive effects. When heated to decomposition it emits toxic fumes of SOx and NOx.

Drug interactions

Potentially hazardous interactions with other drugs Anaesthetics: enhanced hypotensive effect. Antidepressants: additive hypotensive effect with MAOIs - avoid. Antihypertensives: enhanced hypotensive effect. Avanafil, vardenafil, sildenafil and tadalafil: enhanced hypotensive effect - avoid concomitant use. Diuretics: enhanced hypotensive effect. Linezolid: additive hypotensive effect. Moxisylyte: possibly severe postural hypotension.

Metabolism

Phentolamine is extensively metabolised. Only about 10-13% of an intravenous dose is excreted unchanged in the urine, and the fate of the remainder of the drug is unknown.

Check Digit Verification of cas no

The CAS Registry Mumber 65-28-1 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 6 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 65-28:
(4*6)+(3*5)+(2*2)+(1*8)=51
51 % 10 = 1
So 65-28-1 is a valid CAS Registry Number.
InChI:InChI=1/C17H19N3O.CH4O3S/c1-13-5-7-14(8-6-13)20(12-17-18-9-10-19-17)15-3-2-4-16(21)11-15;1-5(2,3)4/h2-8,11,21H,9-10,12H2,1H3,(H,18,19);1H3,(H,2,3,4)

65-28-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (P1985)  Phentolamine Mesylate  >98.0%(HPLC)(T)

  • 65-28-1

  • 100mg

  • 490.00CNY

  • Detail
  • TCI America

  • (P1985)  Phentolamine Mesylate  >98.0%(HPLC)(T)

  • 65-28-1

  • 1g

  • 2,300.00CNY

  • Detail
  • Sigma-Aldrich

  • (PHR1403)  Phentolamine Mesylate  pharmaceutical secondary standard; traceable to USP, PhEur

  • 65-28-1

  • PHR1403-1G

  • 862.41CNY

  • Detail
  • Sigma-Aldrich

  • (Y0001127)  Phentolamine mesilate  European Pharmacopoeia (EP) Reference Standard

  • 65-28-1

  • Y0001127

  • 1,880.19CNY

  • Detail
  • Sigma-Aldrich

  • (Y0001251)  Phentolamine mesilate for system suitability  European Pharmacopoeia (EP) Reference Standard

  • 65-28-1

  • Y0001251

  • 1,880.19CNY

  • Detail
  • Sigma

  • (P7561)  Phentolaminemethanesulfonatesalt  ≥98% (TLC), powder

  • 65-28-1

  • P7561-100MG

  • 966.42CNY

  • Detail
  • Sigma

  • (P7561)  Phentolaminemethanesulfonatesalt  ≥98% (TLC), powder

  • 65-28-1

  • P7561-500MG

  • 3,691.35CNY

  • Detail
  • USP

  • (1530004)  Phentolamine mesylate  United States Pharmacopeia (USP) Reference Standard

  • 65-28-1

  • 1530004-200MG

  • 4,662.45CNY

  • Detail

65-28-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Phentolamine Mesylate

1.2 Other means of identification

Product number -
Other names Phentolamine mesilate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:65-28-1 SDS

65-28-1Synthetic route

methanesulfonic acid
75-75-2

methanesulfonic acid

phentolamine
50-60-2

phentolamine

phentolamine mesylate
65-28-1

phentolamine mesylate

Conditions
ConditionsYield
In ethanol pH=5 - 6;99%
N-(quinolin-8-yl)but‐3‐enamide

N-(quinolin-8-yl)but‐3‐enamide

phentolamine mesylate
65-28-1

phentolamine mesylate

2-(((3-hydroxy-4-(4-oxo-4-(quinolin-8-ylamino)butyl)phenyl)(p-tolyl)amino)methyl)-4,5-dihydro-1Himidazol-3-ium acetate

2-(((3-hydroxy-4-(4-oxo-4-(quinolin-8-ylamino)butyl)phenyl)(p-tolyl)amino)methyl)-4,5-dihydro-1Himidazol-3-ium acetate

Conditions
ConditionsYield
With palladium diacetate; acetic acid In acetonitrile at 120℃; for 4h;33%

65-28-1Downstream Products

65-28-1Relevant articles and documents

Process for synthesis of phentolamine mesylate (by machine translation)

-

Paragraph 033; 0034; 0035; 0036, (2016/10/07)

The invention discloses a synthesis process of phentolamine mesilate. The synthesis process of the phentolamine mesilate comprises the following steps: A, neutralizing, namely, adjusting phentolamine hydrochloride by using diluted ammonia water for many times under the action of silica gel until proper pH value is achieved, and filtering to obtain filtrate to obtain phentolamine free alkali, watering and washing with distilled water for many times until the filtrate is qualified through chloride tracking detection, and drying and crystallizing to obtain a phentolamine free alkali refined product; and B, salifying namely, adding an ethanol solution of methanesulfonic acid into the phentolamine free alkali refined product dropwise by taking absolute ethanol as a solvent, precisely adjusting the pH value to be 5 to 6, then performing a water bath vacuum distillation salt forming reaction, inoculating ethyl acetate, separating out and crystallizing, washing and drying to obtain the phentolamine mesilate. According to the synthesis process of the phentolamine mesilate, the prominent problems that chloride and pH value are not easy to control during actual production are solved, purity is high and impurities are few.

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