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Dopamine hydrochloride

CAS No.
62-31-7
Chemical Name:
Dopamine hydrochloride
Synonyms
DOPAMINE HYDROCHLORIDE;3-HYDROXYTYRAMINE HYDROCHLORIDE;DOPAMINE HCL;2-benzenediol,4-(2-aminoethyl)-hydrochloride;2-(3,4-DIHYDROXYPHENYL)ETHYLAMINE HYDROCHLORIDE;ASL-279;intropin;Dopamin Hcl;Dopamine HCI;dopaminechloride
CBNumber:
CB9243534
Molecular Formula:
C8H12ClNO2
Molecular Weight:
189.64
MDL Number:
MFCD00012898
MOL File:
62-31-7.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 04:53:26
Product description Number Pack Size Price
Dopamine hydrochloride European Pharmacopoeia (EP) Reference Standard D2960000 20 mg $175
Dopamine hydrochloride solution 1.0?mg/mL in methanol with 5% 1 M HCl (as free base), ampule of 1?mL, certified reference material, Cerilliant? D-081 1mL $91
Dopamine hydrochloride British Pharmacopoeia (BP) Reference Standard BP468 100MG $294
Dopamine hydrochloride certified reference material, TraceCERT 43658 50mg $202
Dopamine hydrochloride United States Pharmacopeia (USP) Reference Standard 1225204 200mg $501
More product size

Dopamine hydrochloride Properties

Melting point 248-250 °C(lit.)
Density 1.4 g/cm3
Flash point 11℃
storage temp. Store below +30°C.
solubility alcohol: 20 mg/mL
form Crystalline Powder
color light tan
Water Solubility soluble
Sensitive Air & Light Sensitive
Merck 14,8462
BRN 3656720
Stability Stable. Incompatible with strong oxidizing agents. Combustible.
Major Application pharmaceutical (small molecule)
InChI 1S/C8H11NO2.ClH/c9-4-3-6-1-2-7(10)8(11)5-6;/h1-2,5,10-11H,3-4,9H2;1H
InChIKey CTENFNNZBMHDDG-UHFFFAOYSA-N
SMILES Cl[H].NCCc1ccc(O)c(O)c1
CAS DataBase Reference 62-31-7(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII 7L3E358N9L
EPA Substance Registry System 1,2-Benzenediol, 4-(2-aminoethyl)-, hydrochloride (62-31-7)
UNSPSC Code 41116107
NACRES NA.77

Pharmacokinetic data

Excreted unchanged in urine Minimal
Biological half-life 2 minutes / -

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P301+P312+P330
Hazard Codes  Xi,N,Xn,T,F
Risk Statements  36/37/38-50/53-22-39/23/24/25-23/24/25-11
Safety Statements  26-36-61-45-36/37-16
RIDADR  UN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany  2
RTECS  UX1092000
8-10-23
Hazard Note  Irritant
TSCA  TSCA listed
HS Code  29222900
Storage Class 11 - Combustible Solids
Hazard Classifications Skin Sens. 1
Toxicity LD50 orally in Rabbit: 2859 mg/kg
NFPA 704
1
0 0

Dopamine hydrochloride price More Price(89)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich D2960000 Dopamine hydrochloride European Pharmacopoeia (EP) Reference Standard 62-31-7 20 mg $175 2026-04-30 Buy
Sigma-Aldrich D-081 Dopamine hydrochloride solution 1.0?mg/mL in methanol with 5% 1 M HCl (as free base), ampule of 1?mL, certified reference material, Cerilliant? 62-31-7 1mL $91 2026-04-30 Buy
Sigma-Aldrich BP468 Dopamine hydrochloride British Pharmacopoeia (BP) Reference Standard 62-31-7 100MG $294 2026-04-30 Buy
Sigma-Aldrich 43658 Dopamine hydrochloride certified reference material, TraceCERT 62-31-7 50mg $202 2026-04-30 Buy
Sigma-Aldrich 1225204 Dopamine hydrochloride United States Pharmacopeia (USP) Reference Standard 62-31-7 200mg $501 2026-04-30 Buy
Product number Packaging Price Buy
D2960000 20 mg $175 Buy
D-081 1mL $91 Buy
BP468 100MG $294 Buy
43658 50mg $202 Buy
1225204 200mg $501 Buy

Dopamine hydrochloride Chemical Properties,Uses,Production

Description

Dopamine (hydrochloride) is an endogenous catecholamine neurotransmitter synthesized from the amino acid L-tyrosine that acts as an agonist at dopamine receptors (D1-5). Dopamine is mainly synthesized in the substantia nigra and ventral tegmental area, and is a precursor in norepinephrine and epinephrine biosynthesis. Dopamine-containing neurons in the brain are involved in reward-motivated behavior, motor control, and hormone release. Dopamine is also synthesized in the adrenal glands where it exerts peripheral paracrine functions including control of vasodilation, sodium excretion, insulin production, gastrointestinal motility, and the activity of lymphocytes. Loss or damage of dopaminergic neurons in the substantia nigra is associated with Parkinson’s disease.

Chemical Properties

Dopamine hydrochloride is designated chemically as 3,4-dihydroxyphenethylamine hydrochloride, a white crystalline powder freely soluble in water. It can also be dissolved in hot 95% ethanol, methanol, and sodium hydroxide solution. However, it is insoluble in chloroform, ether, and benzene. It has no odor and a slightly bitter taste. Dopamine (also referred to as 3-hydroxytyramine) is a naturally occurring biochemical catecholamine precursor of norepinephrine.

Uses

Endogenous catecholamine with α and β-adrenergic activity. Cardiotonic; antihypotensive.

Uses

dopaminergic: Dopamine (DA) works as neurotransmitter in the central nervous system. It is a catecholamine made from the amino acid L-tyrosine. It also works as a hormone in vesicles of the adrenal medulla, thereby controlling heart beat rate and blood pressure. Absence of DA-containing neurons is associated with parkinson′s disease.

Uses

A neurotransmitter and vasopressor that modulates cortical activation. Dopamine hydrochloride is a vasopressor that moderates cortical activation. It is used as a precursor to norepinepherine and epinephrine. It is an important neurotransmitter and chemical messenger that helps in the transmission of signals in the brain and other vital areas.

Indications

Dopamine HCl is indicated for the correction of hemodynamic imbalances present in the shock syndrome due to myocardial infarction, trauma, endotoxic septicemia, open-heart surgery, renal failure, and chronic cardiac decompensation as in congestive failure.

Application

Dopamine hydrochloride has been used to study dopamine-mediated transient modulation of the physiological responses in whiteleg shrimp, Litopenaeus vannamei.
It has been used to study dopamine-mediated changes in immunity susceptibility to Lactococcus garvieae in the freshwater giant prawn, Macrobrachium rosenbergii.
It has been used to study the molecular link between dopamine-induced oxidative stress and mHtt (mutant Huntingtin) toxicity in relation to the activation of the autophagy pathway in an 'in vitro' model of parkinsonian Huntington's Disease.

Definition

ChEBI: Dopamine hydrochloride is a catecholamine.

Preparation

Dopamine hydrochloride is produced through the ring-opening reaction of piperonyl ethylamine. Piperethylamine and phenol are added to a reaction vessel and cooled down. Hydrochloric acid is slowly added while heating up the mixture to 110°C, and refluxed for 12-44 hours until the reaction reaches completion. The solution is then slightly cooled and water is added, and the mixture is stirred well and allowed to separate into layers. The upper phenolic layer is then removed, and the aqueous layer is extracted with isopropyl acetate. The extracted aqueous layer is then evaporated under reduced pressure (8.0kPa) until dry. Half the amount of ethanol and hydrochloric acid are added to the dry residue and heated to dissolve. The solution is then cooled, crystallized, and filtered. The filter cake is washed with ethanol and dried to obtain the final product, with a yield of 74%.

brand name

Intropin (Mayne).

General Description

Dopamine Hydrochloride is the hydrochloride salt form of dopamine, a monoamine compound with positive inotropic activity. Dopamine is a neurotransmitter which is a naturally occurring catecholamine. Dopamine hydrochloride salt is indicated as a medicine for the treatment of acute congestive and renal failures.

Biological Activity

Endogenous neurotransmitter that acts as an agonist at dopamine D 1-5 receptors. Synthesized in the substantia nigra and ventral tegmental area, and is a precursor in noradrenalin and adrenalin biosynthesis.

Pharmacokinetics

Dopamine hydrochloride(62-31-7) is a precursor for the synthesis of epinephrine in the body. It has β (mainly β1 receptor) receptor agonism and α receptor agonism, and can also promote the release of norepinephrine. It can enhance myocardial contractility, increase cardiac output, and accelerate the heart rate to a lesser extent (not as obvious as isoproterenol); stimulate the α-receptors of blood vessels in tissues such as skin and muscles, so that blood vessels constrict and blood supply is reduced; it stimulates visceral blood vessels ( The dopamine receptors in the kidney, mesentery, and heart) dilate and increase blood flow. The change of total peripheral resistance is not obvious, but it is beneficial to improve the blood supply of vital organs during shock.

Clinical Use

Cardiogenic shock in infarction or cardiac surgery

target

Dopamine Receptor

Drug interactions

Potentially hazardous interactions with other drugs
Alpha-blockers: avoid with tolazoline.
Anaesthetics: risk of ventricular arrhythmias with isoflurane - avoid.
Antidepressants: risk of hypertensive crisis with MAOIs and moclobemide.
Ciclosporin: may reduce risk of ciclosporin nephrotoxicity
Dopaminergics: effects possibly enhanced by entacapone; avoid with rasagiline; risk of hypertensive crisis with selegiline.

Metabolism

Dopamine is a metabolic precursor of noradrenaline and, whereas a proportion is excreted as the metabolic products of noradrenaline, the majority is mainly metabolised into 3,4,-dihydroxyphenylacetic acid (DOPAC) and 3-methoxy-4-hydroxyphenylacetic (HVA) which are rapidly excreted in the urine.

storage

Store at -20°C

References

[1] C MISSALE. Dopamine receptors: from structure to function.[J]. Physiological reviews, 1998, 78 1: 189-225. DOI: 10.1152/physrev.1998.78.1.189
[2] HAYAISHI O. Molecular genetic studies on sleep-wake regulation, with special emphasis on the prostaglandin D(2) system.[J]. Journal of applied physiology, 2002, 344 1: 863-868. DOI: 10.1152/japplphysiol.00766.2001
[3] CAN D J J. Neuroendocrine Peptide Receptors on Cells of the Immune System[C]. 1992: 0. DOI: 10.1159/000421045
[4] DARIO C. ANGELES. Antioxidants inhibit neuronal toxicity in Parkinson’s disease-linked LRRK2[J]. Annals of Clinical and Translational Neurology, 2016, 3 4: 288-294. DOI: 10.1002/acn3.282

120-20-7
62-31-7
Synthesis of Dopamine hydrochloride from 3,4-Dimethoxyphenethylamine

Dopamine hydrochloride Preparation Products And Raw materials

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1KG 0.99 1000KG Shaanxi Xianhe Biotech Co., Ltd
4-(2-aminoethyl)-pyrocatechohydrochloride dopaminechloride OEM 3-Hydroxytyramine hydrochloride 3-Hydroxytyramine, HCl TIMTEC-BB SBB003668 3,4-DIHYDROXYPHENETHYLAMINE HYDROCHLORIDE 3,4-DIHYDROXYPHENETHYLAMINE, HCL 4-(2-AMINOETHYL)-1-2-BENZENEDIAL HYDROCHLORIDE 4-[2-AMINOETHYL]-1,2-BENZENEDIOL HYDROCHLORIDE 4-(2-AMINOETHYL)PYROCATECHOL HYDROCHLORIDE 3-HYDROXYTYRAMINIUM CHLORIDE 2-(3,4-DIHYDROXYPHENYL)ETHYL-1-13C-AMINE HCL 2-(3,4-DIHYDROXYPHENYL)ETHYLAMINE HYDROCHLORIDE Dopamin Hcl Levomisal Hcl Dopamine-ring-D3HCl 1,2-Benzenediol, 4-(2-aminoethyl)-, hydrochloride 2-(3,4-Dihydroxyphenyl)ethylamine hydrochloride 98% DOPAMINE HC DOPAMINE HCL(RG) Dopamine Hydlrochloride 2-(3,4-Dihydroxyphenyl)ethylamine HCl Dopamine hydrochloride, 3-Hydroxytyramine hydrochloride, 4-(2-Aminoethyl)benzene-1,2-diol hydrochloride 4-(3-aminopropyl)benzene-1,2-diol hydrochloride Dopamine solution Dopamine hydrochloride Solution, 100ppm 2-(3,4-Dihydroxyphenyl)ethylamine hydrochloride, 3,4-Dihydroxyphenethylamine hydrochloride, 3-Hydroxytyramine hydrochloride, 4-(2-Aminoethyl)-1,2-benzenediol hydrochloride Dopamine hydrochloride solution Dopamine hydrochloride (Inotropin) Dopamine Hydrochloride 〔3-Hydroxytyramine Hydrochloride〕 3-Hydroxytyraminium chloride for synthesis Factory supply low price CAS: 62-31-7 Dopamine hydrochloride CAS NO.62-31-7 DOPAMINE HCL CP2000 High quality Dopamine Hydrochloride /Dopamine HCL Powder In stock ,CAS No. 62-31-7 intropin m-hydroxytyraminehydrochloride DOPAMINE HCL DOPAMINE HYDROCHLORIDE HYDROXYTYRAMINE HCL 3,4-DIHYDROXYPHENYL-ETHYLAMINE HYDROCHLORIDE Hydroxyazaniumylidynemethane Pyrocatechol, 4-(2-aminoethyl)-, hydrochloride Dopamine-ring-D3Cl alpha-(3,4-Dihydroxyphenyl)-beta-aminoethane hydrochloride Dopastat KW-3160 3-Hydroxytyramine hydrochloride,99% ASL-279 Cardiosteril α-(3,4-Dihydroxyphenyl)ethylaMMoniuM chloride α-(3,4-Dihydroxyphenyl)β-aMinoethane hydrochloride 3-HydroxytyraMine hydrochloride, 99% 10GR 3-HydroxytyraMine hydrochloride, 99% 25GR 3-Hydroxytyramine hydrochloride,3,4-DihydrophenethylamineHydrochloride Dopamine hydrochloride,2-(3,4-Dihydroxyphenyl)ethylamine hydrochloride, 3,4-Dihydroxyphenethylamine hydrochloride, 3-Hydroxytyramine hydrochloride, 4-(2-Aminoethyl)-1,2-benzenediol hydrochloride Dopamine Hydrochloride (200 mg) 3,4-Dihydroxyphenethylamine hydrochloride 98% 4-(2-Aminoethyl)pyrocatechol Hydrochloride 2-(3,4-Dihydroxyphenyl)ethylamine Hydrochloride Dopamine Hydrochloride