Date published: 2026-5-6

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L-Norepinephrine hydrochloride (CAS 329-56-6)

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Alternate Names:
L-Noradrenaline hydrochloride; (−)-Arterenol hydrochloride
Application:
L-Norepinephrine hydrochloride is an adrenal medullary stress hormone, which mediates the fight-or-flight response
CAS Number:
329-56-6
Molecular Weight:
205.64
Molecular Formula:
C8H11NO3•HCl
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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L-Norepinephrine hydrochloride, often recognized for its pivotal role in neurobiology and molecular research, is a synthetic form of the naturally occurring neurotransmitter norepinephrine, distinguished by the addition of a hydrochloride group to enhance solubility and stability for experimental applications. This compound plays a critical role in the investigation of the sympathetic nervous system′s mechanisms, particularly in understanding how nerve impulses are transmitted across synapses. Its action is primarily through the binding to and activation of adrenergic receptors, which are pivotal in the study of stress responses, learning, and memory formation processes. Researchers leverage L-Norepinephrine hydrochloride as a tool to dissect the intricate pathways of neurotransmission, examining its effects on receptor activation, signal transduction, and neurotransmitter release. This has profound implications for elucidating the molecular underpinnings of a wide array of physiological responses and offers a window into the modulation of these processes at a cellular level, aiding in the advancement of neuroscientific knowledge.


L-Norepinephrine hydrochloride (CAS 329-56-6) References

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  4. Regulation of (Na+, K+) adenosinetriphosphatase of nerve ending membranes: action of norepinephrine and a soluble factor.  |  Rodriguez De Lores Arnaiz, G. and Mistrorigo De Pacheco, M. 1978. Neurochem Res. 3: 733-44. PMID: 216946
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  6. Label-free silver triangular nanoplates for spectrophotometric determination of catecholamines and their metabolites.  |  Zaytsev, VD., et al. 2020. Mikrochim Acta. 187: 610. PMID: 33057848
  7. Some characteristics of an adenyl cyclase preparation from rabbit ciliary process tissue.  |  Waitzman, MB. and Woods, WD. 1971. Exp Eye Res. 12: 99-111. PMID: 4330453
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Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

L-Norepinephrine hydrochloride, 500 mg

sc-279253
500 mg
$553.00