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DL-Norepinephrine Hydrochloride - 97%, high purity , CAS No.55-27-6
Basic Description
Synonyms
1,2-BENZENEDIOL, 4-(2-AMINO-1-HYDROXYETHYL)-, HYDROCHLORIDE, (+/-)- | FT-0673074 | DL-alpha-(Aminomethyl)-3,4-dihydroxybenzyl alcohol | EINECS 200-229-8 | Levarterenol hydrochloride; L-Noradrenaline hydrochloride | EN300-1590673 | NORADRENALINE HYDROCHLOR
Specifications & Purity
≥97%
Storage Temp
Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description
Norepinephrine modulates human dendritic cell activation by altering cytokine release It is suitable adrenergic drug used in the following studies:To investigate the effects of adrenergic drugs on lantern of larval fly; To evaluate the ability of α-adrenergic stimulation in the presence of elevated calcium levels to induce delayed after depolarizations and triggered activity in Purkinje fibers isolated from cat hearts; Simultaneous reduction and surface functionalization of graphene oxide by a one-step poly(norepinephrine) functionalization.
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Phenols
Subclass
Benzenediols
Intermediate Tree Nodes
Not available
Direct Parent
Catechols
Alternative Parents
Aralkylamines 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Benzene and substituted derivatives Secondary alcohols 1,2-aminoalcohols Organopnictogen compounds Monoalkylamines Hydrochlorides Hydrocarbon derivatives Aromatic alcohols
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
Catechol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Aralkylamine - Monocyclic benzene moiety - 1,2-aminoalcohol - Secondary alcohol - Organopnictogen compound - Aromatic alcohol - Alcohol - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Organic oxygen compound - Organic nitrogen compound - Amine - Hydrochloride - Hydrocarbon derivative - Aromatic homomonocyclic compound
Description
This compound belongs to the class of organic compounds known as catechols. These are compounds containing a 1,2-benzenediol moiety.
External Descriptors
Not available
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Associated Targets(Human)
Associated Targets(non-human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
Pubchem Sid
488179962
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488179962
IUPAC Name
4-(2-amino-1-hydroxyethyl)benzene-1,2-diol;hydrochloride
INCHI
InChI=1S/C8H11NO3.ClH/c9-4-8(12)5-1-2-6(10)7(11)3-5;/h1-3,8,10-12H,4,9H2;1H
InChIKey
FQTFHMSZCSUVEU-UHFFFAOYSA-N
Smiles
C1=CC(=C(C=C1C(CN)O)O)O.Cl
Isomeric SMILES
C1=CC(=C(C=C1C(CN)O)O)O.Cl
WGK Germany
3
RTECS
DN6650000
Molecular Weight
205.64
Beilstein
3707003
Reaxy-Rn
4211089
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4211089&ln=
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Solubility
Soluble in water (100 g/l), and DMSO.
Sensitivity
Moisture sensitive
Molecular Weight
205.640 g/mol
XLogP3
Hydrogen Bond Donor Count
5
Hydrogen Bond Acceptor Count
4
Rotatable Bond Count
2
Exact Mass
205.051 Da
Monoisotopic Mass
205.051 Da
Topological Polar Surface Area
86.700 Ų
Heavy Atom Count
13
Formal Charge
0
Complexity
142.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
1
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
2
Citations of This Product
1.
Man Zhang, Rubo Tian, Siyang Tang, Kejing Wu, Binshen Wang, Yingying Liu, Yingming Zhu, Houfang Lu, Bin Liang.
(2023)
The structure and properties of lignin isolated from various lignocellulosic biomass by different treatment processes.
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,
243
(125219).
2.
Wei Luo, Teris A. van Beek, Bo Chen, Han Zuilhof, Gert IJ. Salentijn.
(2022)
Boronate affinity paper spray mass spectrometry for determination of elevated levels of catecholamines in urine.
ANALYTICA CHIMICA ACTA,
1235
(340508).
3.
Tian Wang, Boya Hao, Shilin Xu, Jie Meng, Tao Wen, Jian Liu, Haiyan Xu.
(2022)
Effective RNAi in leukemia cells is enhanced by spermine-modified pullulan combined with desloratadine.
CARBOHYDRATE POLYMERS,
292
(119646).
4.
He Maofang, Wei Yinmao, Wang Rong, Wang Chunyang, Zhang Bo, Han Lu.
(2019)
Boronate affinity magnetic nanoparticles with hyperbranched polymer brushes for the adsorption of cis-diol biomolecules.
MICROCHIMICA ACTA,
186
(10):
(1-9).
5.
Lingsha Cheng, Haoqian Wu, Xiaoying Cai, Youying Zhang, Siqi Yu, Yuanlong Hou, Zhe Yin, Qingyuan Yan, Qiong Wang, Taipeng Sun, Guangji Wang, Yonggui Yuan, Xueli Zhang, Haiping Hao, Xiao Zheng.
(2024)
A Gpr35-tuned gut microbe-brain metabolic axis regulates depressive-like behavior.
Cell Host & Microbe,
6.
Wei Wei, Yali Liu, Yuanlong Hou, Shuqi Cao, Zhuo Chen, Youying Zhang, Xiaoying Cai, Qingyuan Yan, Ziguang Li, Yonggui Yuan, Guangji Wang, Xiao Zheng, Haiping Hao.
(2024)
Psychological stress-induced microbial metabolite indole-3-acetate disrupts intestinal cell lineage commitment.
Cell Metabolism,
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