Ambroxol HCl - 2mM in DMSO , CAS No.23828-92-4

CAS: 23828-92-4 Cat. No.: A408443 Summenformel: C13H18Br2N2O·HCl Molekulargewicht: 414.56 EG-Nummer: 245-899-2
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GRADE & PURITY 2mM in DMSO
Synonyms
Cyclohexanol, 4-[[(2-amino-3,5-dibromophenyl)methyl]amino]-, hydrochloride (1:1), trans-
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Size
Deutschland (EU)
USA*
Price
Qty
1ml
A408443-1ml
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2 Auf Lager

29,42€

34,62€
Speichern 5,21 € (15.04%)
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Why this grade

2mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Übersicht

Information

Ambroxol HCl AmbroxolHCl is a potent inhibitor of the neuronal Na+ channels , inhibits TTX-resistant Na+ currents with IC50 of 35.2 μM and 22.5 μM for tonic and phasic block, inhibits TTX-sensitive Na+ currents with IC50 of 100 μM. Phase 3.
In vitro

Ambroxol inhibits Na+ channels in sensory neurons. The potency for tonic block of TTX-r channels is relatively high. Ambroxol affects the Na+ current kinetics of TTX-r and TTX-s channels differently. In CNaIIA cells, the compound behaves like a charged local anesthetic: the block is dependent on stimulus number and increases with higher frequencies in a train of depolarizing stimuli. In CNaIIA cells, ambroxol inhibits inactivated channels 5.5-fold more potently than resting channels. The corresponding factor for TTX-r channels is only 3.3. Ambroxol inhibits the release of histamine, leukotrienes and cytokines from human leukocytes and mast cells.

In vivo

Ambroxol inhibited histamine release by more than 50% from human adenoidal mast cells (1000 microM ambroxol) and skin mast cells (100 microM ambroxol) stimulated by Con A and compound 48/80, respectively. Ambroxol (100 microM) strikingly inhibited anti-IgE induced release of both histamine, LTC4, IL-4 and IL-13 from basophils and reduced both histamine and LTB4 release induced by C5a or Zymosan in monocytes. The drug also reduced LTB4 and superoxide anion production in granulocytes stimulated by zymosan or fMLP.
Cell Data

cell lines:

Concentrations:

Incubation Time:

Powder Purity:≥99%

Specifications

Synonyme
Cyclohexanol, 4-[[(2-amino-3,5-dibromophenyl)methyl]amino]-, hydrochloride (1:1), trans-
Spezifikationen & Reinheit
2mM in DMSO
Biochemische und physiologische Mechanismen
AmbroxolHCl is a potent inhibitor of the neuronal Na+ channels, inhibits TTX-resistant Na+ currents with IC50 of 35.2 μM and 22.5 μM for tonic and phasic block, inhibits TTX-sensitive Na+ currents with IC50 of 100 μM. Phase 3.
Storage
Store at -80°C
Verschickt in
Dry ice packs + Cold packs
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Namen und Kennungen
Isomere SMILES C1CC(CCC1NCC2=C(C(=CC(=C2)Br)Br)N)O.Cl
RTECS GV8425000
Alternative CAS-Nummer 18683-91-5
Molekulargewicht 414.56
Reaxy-Rn 6882396
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=6882396&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemische und physikalische Eigenschaften
Schmelzpunkt (°C)235°C(dec.)(lit.)
Citations of This Product
Referenzen
1. Yushi Ding, Suyun Yu, Zhonghong Wei, Rui Deng, Peng Chen, Yifan Sun, Qi Jia, Xiaoman Li, Yuanyuan Wu, Wenxing Chen, Kurt S. Zanker, Aiyun Wang, Yin Lu.  (2020)  Relieving Sore Throat Formula Exerts a Therapeutic Effect on Pharyngitis through Immunoregulation and NF-κB Pathway.  MEDIATORS OF INFLAMMATION,      [PMID:32508523] [10.1155/2020/2929163]
2. Sovichea Lay, Hai-ning Yu, Bao-xiang Hu, Sheng-rong Shen.  (2016)  Molecularly imprinted polymers as the extracted sorbents of clenbuterol ahead of liquid chromatographic determination.  Journal of Zhejiang University-SCIENCE B,      [PMID:27256680] [10.1631/jzus.B1500225]
3. Binbin Shao, Chenkai Hu, Hainan Zhao, Chengcheng Xiao, Erdeng Du, Anhong Cai, Jing Deng.  (2024)  Degradation of ambroxol by UV/chloramine process: Kinetics, degradation pathway, and control of the risk of highly toxic disinfection by-products.  ENVIRONMENTAL POLLUTION,      [PMID:39393762] [10.1016/j.envpol.2024.125091]
4. Fan Zhang, Yajie Ma, Jie Mei, Xinrong Xie, Xiaoyan Wang, Yuanyuan Zhang, Boyang Yu.  (2026)  Complementary Roles and Synergy of the Ephedra-Glycyrrhiza Herb Pair Across Murine Models of Respiratory Symptoms and Poly(I:C)-Induced Pneumonia.  PHYTOMEDICINE,      [PMID:41539102] [10.1016/j.phymed.2026.157795]
5. Zheng Xiong, Niu Qiuqi, Cui Zihan, Sun Chuanzhi, Long Min, Wu Yang, Chen Yinguang.  (2026)  Functional Groups in Pharmaceutical Contaminants Reshape Sludge Fermentation Pathways: Substrate Selectivity and Microbial Stress Responses.  ENVIRONMENTAL SCIENCE & TECHNOLOGY,      [PMID:] [10.1021/acs.est.6c01101]
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