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Chemical structure of CAS 588-05-6

m-Tyramine

In Stock•Starting at $66 for 50 mg•Purity ≥ 95%
CAS No.588-05-6
MDL No.N/A
MFC8H11NO
MW137.18
InChI KeyGHFGJTVYMNRGBY-UHFFFAOYSA-N
CUSTOM SYNTHESIS

Pricing & Availability

Pack SizePurityPriceAvailabilityAction
50 mg≥95%$66In Stock
100 mg95%$93In Stock
250 mg95%$170In Stock
1 g95%$238In Stock
Custom synthesis and bulk supply options are available upon request.

Product Information

M-tyramine is a primary amino compound, specifically 2-phenylethanamine with a hydroxy group at position 3. It functions as a human urinary metabolite and neurotransmitter, belonging to the tyramine family and acting as the conjugate base of m-tyraminium.

CAS No.588-05-6
Product Namem-Tyramine
CorrosiveCorrosive
IrritantIrritant
Signal Word:Danger
HCode:H302-H318
PCode:P264-P264+P265-P270-P280-P301+P317-P305+P354+P338-P317-P330-P501

Related Articles

Studies related to this compound and its mechanism of action

Calcium-promoted Pictet-Spengler reactions of ketones and aldehydes.

The Journal of organic chemistry • Vol. 75, Issue 24 • 2010
PMID: 21090691DOI: 10.1021/jo1019283

Human and mouse trace amine-associated receptor 1 have distinct pharmacology towards endogenous monoamines and imidazoline receptor ligands.

The Biochemical journal • Vol. 424, Issue 1 • 2009
PMID: 19725810DOI: 10.1042/BJ20090998

Covalent and noncovalent chemical modifications of arginine residues decrease dopamine transporter activity.

Synapse (New York, N.Y.) • Vol. 52, Issue 4 • 2004
PMID: 15103693DOI: 10.1002/syn.20021

Solid-phase synthesis of 1-substituted tetrahydroisoquinoline derivatives employing BOC-protected tetrahydroisoquinoline carboxylic acids.

Journal of combinatorial chemistry • Vol. 6, Issue 4 • 2004
PMID: 15244409DOI: 10.1021/cc0340776

Documentation

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