ChemicalBook >> CAS DataBase List >>Minoxidil

Minoxidil

CAS No.
38304-91-5
Chemical Name:
Minoxidil
Synonyms
Minoxidil Base;pdp;Minoxidil powder;2,4-diamino-6-piperidinopyrimidine3-n-oxide;rogaine;minoxidi;Minoxidil CRS;4-pyrimidinediamine;Minoxidil for system suitability;Minoxidil for system suitability CRS
CBNumber:
CB7383531
Molecular Formula:
C9H15N5O
Molecular Weight:
209.25
MDL Number:
MFCD00063409
MOL File:
38304-91-5.mol
MSDS File:
SDS
Last updated:2024-04-19 20:05:26

Minoxidil Properties

Melting point 272-274 °C (dec.) (lit.)
Boiling point 348.61°C (rough estimate)
Density 1.1651 (rough estimate)
refractive index 1.7610 (estimate)
storage temp. 2-8°C
solubility Slightly soluble in water, soluble in methanol and in propylene glycol.
pka 4.61(at 25℃)
color White
Water Solubility Soluble in water (2.2 mg/ml), 100% ethanol (29 mg/ml), propylene glycol, acetone, DMSO (6.5 mg/ml), and methanol.
Merck 14,6203
BCS Class 3
Stability Stable for 2 years from date of purchase as supplied. Protect from moisture. Solutions in DMSO or ethanol may be stored at -20°C for up to 3 months.
InChIKey ZFMITUMMTDLWHR-UHFFFAOYSA-N
CAS DataBase Reference 38304-91-5(CAS DataBase Reference)
EWG's Food Scores 1-3
FDA UNII 5965120SH1
NIST Chemistry Reference Minoxidil(38304-91-5)
ATC code C02DC01,D11AX01
Pesticides Freedom of Information Act (FOIA) Triclosan, Irgasan

Pharmacokinetic data

Excreted unchanged in urine 15-20%
Volume of distribution 2-3(L/kg)
Biological half-life 4.2 / 8.9

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P301+P312+P330-P305+P351+P338
Hazard Codes  Xn,T+
Risk Statements  22-36/37/38-26/27/28
Safety Statements  26-36-45-36/37/39-22
WGK Germany  3
RTECS  UV8200000
HS Code  29335990
Toxicity LD50 in rats, mice (mg/kg): 49, 51 i.v. (Carlson, Feenstra)
NFPA 704
0
2 0

Minoxidil price More Price(49)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich M4145 Minoxidil ≥99% (TLC) 38304-91-5 25mg $88.8 2024-03-01 Buy
Sigma-Aldrich PHR2123 Minoxidil Pharmaceutical Secondary Standard; Certified Reference Material 38304-91-5 200MG $186 2024-03-01 Buy
Sigma-Aldrich BP637 Minoxidil British Pharmacopoeia (BP) Reference Standard 38304-91-5 100MG $262 2024-03-01 Buy
Sigma-Aldrich 1444208 Minoxidil United States Pharmacopeia (USP) Reference Standard 38304-91-5 125mg $358 2024-03-01 Buy
TCI Chemical M1389 Minoxidil >98.0%(HPLC)(T) 38304-91-5 1g $33 2024-03-01 Buy
Product number Packaging Price Buy
M4145 25mg $88.8 Buy
PHR2123 200MG $186 Buy
BP637 100MG $262 Buy
1444208 125mg $358 Buy
M1389 1g $33 Buy

Minoxidil Chemical Properties,Uses,Production

an antihypertensive vasodilator medication

Minoxidil is an antihypertensive vasodilator medication also claiming to slow or stop hair loss and promote hair regrowth. It is available over the counter for treatment of androgenic alopecia, among other baldness treatments, but measurable changes, if experienced, disappear within months after discontinuation of treatment.
Minoxidil was first sold as a drug for high blood pressure and was noted to have the interesting side-effect of increased body hair-growth, or in some cases, significant hair loss. Treatments for baldness and hair loss usually include a 5% concentration solution that is designed for men, whereas the 2% concentration solutions are designed for women.

Indications and Usage

Minoxidil is a type of oral drug that is clinically used to lower blood pressure, and it is also called Loniten and piperidine diamine. Minoxidil is an antihypertensive drug that is clinically used to treat intractable, primary or renal hypertension. It can also be used to treat severe hypertension that does not respond well to other antihypertensive drugs, but it needs to be used in combination with diuretic drugs to prevent water and sodium retention, and combined use with beta receptor blockers may increase its curative effects and reduce adverse effects. Minoxidil is also used to prevent grease-type alopecia and on livestock.

Mechanisms of Action

Minoxidil is a type of potassium channel opener and can directly relax smooth vascular muscles and has a strong small artery dilating effect. It can reduce peripheral resistance, dilate blood vessels, and lower blood pressure while having no effect on blood volume, thus promoting venous return. In addition, due to reflective regulation and positive frequency effects, it can increase cardiac output and heart rate, but will not cause orthostatic hypotension.

Adverse reactions

Long term use of Minoxidil may have the side effect of increased body hair, such as arm hair.
Adverse reactions to oral intake mainly include: weight gain and lower body swelling due to water and sodium retention, heart palpitations and arrhythmia due to reflexive sympathetic nervous excitement, and hirsuitism.
Adverse reactions to external use mainly include: skin irritation, red spots in applied areas, itching, and other skin inflammation reactions. Although only a small amount is absorbed, but there is also a slight possibility of causing a recurrence in patients with a history or heart disease. Use with caution if suffering from cerebrovascular disease, non-hypertensive heart failure, coronary heart disease, angina pectoris, myocardial infarction, pericardial effusion, renal dysfunction and other diseases.

Contradictions

Do not use if allergic to Minoxidil or suffering from pheochromocytoma.

Description

Minoxidil is a peripheral vasodilator that directly relaxes vascular smooth musculature, thus, lowering systolic and diastolic pressure. Its action is linked to the activation of calcium channels. Open calcium channels cause hyperpolarization of smooth muscle cells, which in turn, reduces the flow of calcium ions into the cell, which is necessary for supporting vascular tonicity. However, when taking minoxidil, tachycardia, elevated renin secretion, and water and sodium ion retention all appear simultaneously with hypotension.

Chemical Properties

White Crystalline Solid

Originator

Loniten ,Upjohn ,US ,1979

Uses

A selective ATP dependent K+ (Kir6) channel activator

Uses

Used as an antihypertensive and antialopecia agent. Minoxidil activates ATP-activated K+ channels

Definition

ChEBI: Minoxidil is a pyrimidine N-oxide that is pyrimidine-2,4-diamine 3-oxide substituted by a piperidin-1-yl group at position 6. It has a role as a vasodilator agent and an antihypertensive agent. It is a pyrimidine N-oxide, a member of piperidines and an aminopyrimidine.

Manufacturing Process

Barbituric acid is reacted with phosphorus oxychloride then with 2,4,6-trichloropyrimidine and that product with ammonia to give 4-chloro-2,6-diaminopyritnidine.
A 30 g (0.15 mol) quantity of 4-chloro-2,6-diaminopyrimidine is dissolved in600 ml of hot 3A alcohol, the solution cooled to 0°C to 10°C and 41.8 g (0.24mol) of m-chloroperbenzoic acid is added. The mixture is held at 0°C to 10°Cfor 4 hours and filtered. The solid is shaken for 2 hours in 0.24 mol of 10%sodium hydroxide and filtered. The solid is washed with water and dried toyield 193 g of crude product. This product is extracted for 1 hour with 900 mlof boiling acetonitrile to yield 14.8 g (44.7% yield) of 6-amino-4-chloro-1,2-dihydro-1-hydroxy-2-iminopyrimidine, melting point 193°C.
A mixture of 3.0 g (0.019 mol) of 6-amino-4-chloro-1,2-dihydro-1-hydroxy-2-iminopyrimidine and 35 ml of piperidine is refluxed for 1.5 hours, cooled andfiltered. The solid is shaken for 20 minutes in a solution of 0.8 g of sodiumhydroxide in 30 ml of water and filtered. The solid is washed with water andextracted with 800 ml of boiling acetonitrile and filtered to yield 3.5 g (89%)yield of 6-amino-4-chloro-1,2-dihydro-1-hydroxy-2-iminopyrimidine, meltingpoint 248°C, decomposition at 259°C to 261°C.

brand name

Loniten (Pharmacia & Upjohn); Rogaine (Pharmacia & Upjohn); Minodyl (Quantum Pharmics).

Therapeutic Function

Antihypertensive

General Description

Minoxidil, 2,4-diamino-6-piperidinopyrimidine-3-oxide . It is converted to minoxidil sulfate in the liver bya sulfotransferase enzyme.
The antihypertensive properties of minoxidil are similarto those of hydralazine hydrochloride, in that minoxidil candecrease arteriolar vascular resistance. Minoxidil exerts itsvasodilatory action by a direct effect on arteriolar smoothmuscle and appears to have no effect on the CNS or on theadrenergic nervous system in animals. The serum half-lifeis 4.5 hours, and the antihypertensive effect may last up to24 hours.

Biological Activity

Antihypertensive. Antialopecia agent. K + channel (K ATP ) activator.

Biochem/physiol Actions

Activates ATP-activated K+ channels; vasodilator; slow or stop hair loss and promote hair regrowth.

Mechanism of action

Potassium channel openers are drugs that activate (i.e., open) ATP-sensitive K+ channels in the VSM. By opening these potassium channels, there is increased efflux of potassium ions from the cells, causing hyperpolarization of VSM, which closes the voltage-gated calcium channels and, thereby, decreases intracellular calcium. With less calcium available to combine with calmodulin, there is less activation of MLCK and phosphorylation of myosin light chains. This leads to relaxation and vasodilation. Because small arteries and arterioles normally have a high degree of smooth muscle tone, these drugs are particularly effective in dilating these resistance vessels, decreasing systemic vascular resistance, and lowering arterial pressure. The fall in arterial pressure leads to reflex cardiac stimulation (baroreceptor-mediated tachycardia).
Minoxidil, as its active metabolite minoxidil O-sulfate, prolongs the opening of the potassium channel, sustaining greater vasodilation on arterioles than on veins. The drug decreases blood pressure in both the supine and standing positions, and there is no orthostatic hypotension. Associated with the decrease in peripheral resistance and blood pressure is a reflex response that is accompanied by increased heart rate, cardiac output, and stroke volume, which can be attenuated by the coadministration of a β-blocker. Along with this decrease in peripheral resistance is increased plasma renin activity and sodium and water retention, which can result in expansion of fluid volume, edema, and congestive heart failure. The sodium- and water-retaining effects of minoxidil can be reversed by coadministration of a diuretic. When minoxidil is used in conjunction with a β-adrenergic blocker, pulmonary artery pressure remains essentially unchanged.

Pharmacokinetics

Minoxidil is absorbed from the GI tract and is metabolized to its active sulfate metabolite. Plasma concentrations for minoxidil sulfate peak within 1 hour and then decline rapidly. Following an oral dose of minoxidil, its hypotensive effect begins in 30 minutes, is maximal in 2 to 8 hours, and persists for approximately 2 to 5 days. The delayed onset of the hypotensive effect for minoxidil is attributed to its metabolism to its active metabolite. The drug is not bound to plasma proteins. The major metabolite for minoxidil is its N-O-glucuronide, which unlike the sulfate metabolite is inactive as a hypotensive agent. Approximately 10 to 20% of an oral dose of minoxidil is metabolized to its active metabolite, minoxidil O-sulfate, and approximately 20% of minoxidil is excreted unchanged.

Clinical Use

Minoxidil is used for severe hypertension that is difficultto control with other antihypertensive agents. The drug hassome of the characteristic side effects of direct vasodilatorydrugs. It causes sodium and water retention and may requirecoadministration of a diuretic. Minoxidil also causes reflextachycardia, which can be controlled by use of a -adrenergicblocking agent.
Minoxidil topical solution is used to treat alopecia androgenitica(male-pattern baldness). Although the mechanismis not clearly understood, topical minoxidil is believed to increasecutaneous blood flow, which may stimulate hairgrowth. The stimulation of hair growth is attributed to vasodilationin the vicinity of application of the drug, resultingin better nourishment of the local hair follicles.

Side effects

Adverse reactions include local irritation and contact dermatitis. If the treatment is discontinued, clinical regression occurs within 3 months to the state of hair thinning that would have occurred had the treatment not been started. Twice-daily treatment is more efficacious than once-daily application. Women who use the5%concentrationmay note the development of facial hair, which is reversible on discontinuation of the medication. The 5% concentration can be more irritating than the 2% solution.

Synthesis

Minoxidil, 6-amino-1,2-dihydro-1-hydroxy-2-imino-4-piperidinopyrimidine (22.8.5), is synthesized from barbituric acid, the reaction of which with phosphorous oxychloride gives 2,4,6-trichloropyrimidine (22.8.1). Upon reaction with ammonium, this turns into 2,4-diamino-6-chloropyrimidine (22.8.2). Next, the resulting 2,4-diamino-6- chloropyrimidine (22.8.2) undergoes reaction with 2,4-dichlorophenol in the presence of potassium hydroxide, giving 2,4-diamino-6-(2,4-dichlorophenoxy)-pyrimidine (22.8.3). Oxidation of this product with 3-chloroperbenzoic acid gives 2,4-diamino-6-(2,4- dichlorophenoxy)pyrimidine-3-oxide (22.8.4), the 2,4-dichlorophenoxyl group of which is replaced with a piperidine group at high temperature, giving minoxidil (22.8.5).

Synthesis_38304-91-5

Drug interactions

When minoxidil is administered with diuretics or other hypotensive drugs, the hypotensive effect of minoxidil increases, and concurrent use may cause profound orthostatic hypotensive effects.

Metabolism

Extensively metabolised by the liver. It requires sulphation to become active, but the major metabolite is a glucuronide conjugate. Excreted mainly in the urine in the form of metabolites. Minoxidil and its metabolites are dialysable, although the pharmacological effect is not reversed.

storage

Room temperature

References

1) Meisheri et al. (1988), Mechanism of action of minoxidil sulfate-induced vasodilation: a role for increased K+ permeability; J. Pharmacol. Exp. Ther., 245 7 2) Messenger and Rundegren (2004) Minoxidil:mechanisms of action on hair growth; Br. J. Dermatol., 150 186

110-89-4
35139-67-4
38304-91-5
Synthesis of Minoxidil from Piperidine and 2,6-Diamino-4-chloropyrimidine 1-oxide
Global( 734)Suppliers
Supplier Tel Email Country ProdList Advantage
Xi'an Kono chem co., Ltd.,
029-86107037 13289246953 info@konochemical.com China 2995 58
Baoji Guokang Bio-Technology Co., Ltd.
0917-3909592 13892490616 gksales1@gk-bio.com China 9339 58
Lihe Pharm Technology(Wuhan)Co.,Ltd
+8618071517867 info@lihepharma.com China 194 58
XI'AN TIANGUANGYUAN BIOTECH CO., LTD.
+86-029-86333380 18829239519 sales06@tgybio.com China 961 58
Sinoway Industrial co., ltd.
0592-5800732; +8613806035118 xie@china-sinoway.com China 992 58
Guangzhou Tengyue Chemical Co., Ltd.
+86-86-18148706580 +8618826483838 evan@tyvovo.com China 152 58
Shanghai Affida new material science and technology center
+undefined15081010295 2691956269@qq.com China 359 58
Shanghai Aosiris new Material Technology Co., LTD
+8615139564871 wrjmoon2000@163.com China 354 58
Dorne Chemical Technology co. LTD
+86-13583358881 +86-18560316533 Ethan@dornechem.com China 293 58
Hebei Lingding Biotechnology Co., Ltd.
+86-18031140164 +86-19933155420 erin@hbldbiotech.com China 879 58

Related articles

  • The effect of Minoxidil on hair
  • Minoxidil is a cosmetic drug recognized as a mitogenic agent, which may be potential mutagenic and carcinogenic agent.
  • Nov 10,2023

View Lastest Price from Minoxidil manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Minoxidil pictures 2024-04-19 Minoxidil
38304-91-5
US $3.00-1.00 / kg 1kg 99.9% 10 tons Shanghai Aosiris new Material Technology Co., LTD
Minoxidil pictures 2024-04-19 Minoxidil
38304-91-5
US $1.00 / g 1g 99% 1000kg Dorne Chemical Technology co. LTD
Minoxidil 5% solution pictures 2024-04-19 Minoxidil 5% solution
38304-91-5
US $35.00 / KG 20KG 99% 1000 Hebei Yime New Material Technology Co., Ltd.
  • Minoxidil pictures
  • Minoxidil
    38304-91-5
  • US $3.00-1.00 / kg
  • 99.9%
  • Shanghai Aosiris new Material Technology Co., LTD
  • Minoxidil pictures
  • Minoxidil
    38304-91-5
  • US $1.00 / g
  • 99%
  • Dorne Chemical Technology co. LTD
6-amino-1,2-dihydro-1-hydroxy-2-imino-4-piperidinopyrimidine 6-piperidino-2,4-diaminopyrimidine3-oxide alopexil alostil lonolox minossidile minoximen prexidil regaine tricoxidil 2,6-diaMino-4-(piperidin-1-yl)-1$l^{5},3-pyriMidin-1-one Minoxidil (U-10858) Minoxidil/2,4-DiaMino-6-piperidino-pyriMidine-3-oxide 2,6-Diamino-4-(piperidin-1-yl)pyrimidine 1-oxide 2,3-dihydro-3-hydroxy-2-imino-6-(1-piperidinyl)-4-pyrimidinamine 2,4-diamino-6-piperidinilpirimidina-3-ossido [Pyruvate dehydrogenase [acetyl-transferring]]-phosphatase 1, mitochondrial ANTI-PDP1 (CENTER) antibody produced in rabbit PPM2C Minoxidil, Loniten,Lonolox,Lonoten,Minona inoxidil regain MONOXIDIL MINOXIDIL U-10858 2,4-DIAMINO-6-PIPERIDINOPYRIMIDINE 3-OXIDE 6-(1-PIPERIDINYL)-2,4-PYRIMIDINEDIAMINE 3-OXIDE 6-(1-PIPERIDINYL)PYRIMIDINE-2,4-DIAMINE 3-OXIDE loniten Minoidil MINOXIDIL EP, BP, USP MINOXIDIL K+ CHANNEL ACTIVATOR, MethylPhosphateEster 2,4-Pyrimidinediamine, 6-(1-piperidinyl)-, 3-oxide MINOXIDIL,POWDER,USP TRICLOSAN (IRGASAN) Minoxidil (Subject To Patent Free) 6-(1-Piperidinyl)-2,4-pyrimidinediamine 3-oxide, 6-(1-Piperidinyl)pyrimidine-2,4-diamine 3-oxide Minoxidil,6-(1-Piperidinyl)-2,4-pyrimidinediamine 3-oxide, 6-(1-Piperidinyl)pyrimidine-2,4-diamine 3-oxide Minoxidil (125 mg) Aalopexil 2,4-diamino-6-piperidino-pyrimidin3-oxide 2,6-diamino-4-(piperidin-1-yl)pyrimidin-1-ium-1-olate Minoxidil, 98%, vasodilator agent LONTEN Minoxidil> Minoxidil powder/Minoxidil 6-(piperidin-1-yl)pyrimidine-2,4-diamine 3-oxide Minoxidil Solution in Methanol, 100μg/mL minoxcidil 2,6-Diamino-4-piperidinopyrimidine 1-Oxide Minoxidil USP/EP/BP Minoxidil 5% solution Latilavir side chain Pure Minoxidil powder Sonwu CAS?38304-91-5?of Minoxidil Powder MINOⅪDIL Pharmaceutical Minoxidil