ADRENOCHROME structure, CAS 54-06-8

ADRENOCHROME

CAS Number54-06-8

Synonymsadrenochrome

Molecular FormulaC9H9NO3

Molecular Weight179.17

Purity≥95 (HPLC)%

Density1.42g/cm3

Boiling Point375.1ºC at 760 mmHg

Melting Point115-120ºC

Flash Point

Appearancepowder

EINECS200-192-8

MSDSChineseEnglish

Symboltransportation

Signal WordWarning

Cat. No.: 2A-1194634 Purity: ≥95 (HPLC)%
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Quality Control of [ 54-06-8 ] Purity: ≥95 (HPLC)% SDS Specification MoL

Chemical & Physical Properties
CAS Number54-06-8
Catalog No.2A-1194634
Chinese Name肾上腺色素
Synonymsadrenochrome
Molecular FormulaC9H9NO3
Molecular Weight179.17
Purity≥95 (HPLC)
Density1.42g/cm3
Boiling Point375.1ºC at 760 mmHg
Melting Point115-120ºC
Appearancepowder
Storage ConditionThe warehouse is ventilated and dried at low tempe
ApplicationAdrenochrome (Adraxone) is the oxidation product of adrenaline. Adrenochrome is a potent constrictor of coronary arteries in the rat heart. Adrenochrome can be used in the study of neurological diseas
EINECS200-192-8
HTC2933990090
PubChem ID24891016
MDL NumberMFCD00069732
SMILESCN1CC(O)C2=CC(=O)C(=O)C=C12
InChI1S/C9H9NO3/c1-10-4-9(13)5-2-7(11)8(12)3-6(5)10/h2-3,9,13H,4H2,1H3
InChI KeyRPHLQSHHTJORHI-UHFFFAOYSA-N
NACRES CodeNA.47
UNSPSC12171500
Hazard Symbolstransportation
MSDSmsds/196315_1_54_06_8.pdf
BioactivityAdrenochrome (Adraxone) is an oxidation product of Epinephrine. Adrenochrome is a potent coronary constricting agent in the rat heart. Adrenochrome can be used for neurological disorder research[1][2][3]. Related Catalog Research Areas >> Cardiovascular Disease Signaling Pathways >> Others >> Others Research Areas >> Neurological Disease In Vitro Adrenochrome decreases microsomal calcium binding, calcium uptake and Ca2+-stimulated Mg2+-dependent ATPase activities. The inhibitory effect of Adrenochrome on microsomal calcium uptake activity of the isolated membrane is independent of pH (6.0-8.0), calcium concentrations (10-200 μM), protein concentration (0.02-0.10 mg/mL), temperature (25-37 degrees C) and incubation time (2-30 min)[2]. In Vivo In isolated rat hearts, concentrations of Adrenochrome from 1 to 1000 ng/mL increases coronary pressure in a dose- and time-dependent manner. Furthermore, the degree of constriction by Adrenochrome is dependent on the CaCl2 concentration in the perfusion medium[1]. References [1]. M Karmazyn,, et al. Adrenochrome-induced coronary artery constriction in the rat heart. J Pharmacol Exp Ther. 1981 Oct;219(1):225-30. [2]. S Takeo,et al. Effects of adrenochrome on calcium accumulating and adenosine triphosphatase activities of the rat heart microsomes. J Pharmacol Exp Ther. 1980 Sep;214(3):688-93. [3]. Koji Ueda, et al. Catecholamine oxidation-mediated transcriptional inhibition in Mn neurotoxicity. J Toxicol Sci. 2020;45(10):619-624. Chemical & Physical Properties Density 1.42g/cm3 Boiling Point 375.1ºC at 760 mmHg Melting Point 115-120ºC Molecular Formula C9H9NO3 Molecular Weight 179.17300 Flash Point 180.7ºC Exact Mass 179.05800 PSA 57.61000 Index of Refraction 1.63 InChIKey RPHLQSHHTJORHI-UHFFFAOYSA-N SMILES CN1CC(O)C2=CC(=O)C(=O)C=C21
Use ofAdrenochrome (Adraxone) is an oxidation product of Epinephrine. Adrenochrome is a potent coronary constricting agent in the rat heart. Adrenochrome can be used for neurological disorder research[1][2][3]. Properties Articles29 Name 3-Hydroxy-1-methyl-5,6-indolinedione Synonym More Synonyms ADRENOCHROME Biological Activity Description Adrenochrome (Adraxone) is an oxidation product of Epinephrine. Adrenochrome is a potent coronary constricting agent in the rat heart. Adrenochrome can be used for neurological disorder research[1][2][3]. Related Catalog Research Areas >> Cardiovascular Disease Signaling Pathways >> Others >> Others Research Areas >> Neurological Disease References [1]. M Karmazyn,, et al. Adrenochrome-induced coronary artery constriction in the rat heart. J Pharmacol Exp Ther. 1981 Oct;219(1):225-30. [2]. S Takeo,et al. Effects of adrenochrome on calcium accumulating and adenosine triphosphatase activities of the rat heart microsomes. J Pharmacol Exp Ther. 1980 Sep;214(3):688-93. [3]. Koji Ueda, et al. Catecholamine oxidation-mediated transcriptional inhibition in Mn neurotoxicity. J Toxicol Sci. 2020;45(10):619-624. Chemical & Physical Properties Molecular Formula C9H9NO3 Exact Mass 179.05800 PSA 57.61000 Index of Refraction 1.63 InChIKey RPHLQSHHTJORHI-UHFFFAOYSA-N
Tax Rebate13.0%
SupervisionNone. MFN tariff: 6.5%. Ordinary tariff: 20.0%
Transport InfoProduct name: Purity: 99.0%
MSDS Transport InfoModule 14. Shipping information 14.1 UN number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 Names specified by the United Nations (UN) European Land Transport Dangerous Regulations: No dangerous goods IMDG Code: No dangerous goods International Air Transport Dangerous Regulations: No dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Dangerous Regulations: No International Maritime Transport Dangerous Regulations Maritime Pollutants: No International Air Transport Risk Regulations: No 14.6 Special precautions for users No data available The company is not responsible for any damage caused by any operation or contact with the above products. For more terms of use, see invoice or package The reverse side of the mounting strip.
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