Atropine sulfate monohydrate - 10mM in DMSO , CAS No.5908-99-6

CAS: 5908-99-6 Cat. No.: A408832 Peso molecular: 694.83 Beilstein Registry Number: 6109275 Número EC: 611-792-8
Disponible para pedir
GRADE & PURITY 10mM in DMSO
Synonyms
α-​(hydroxymethyl)​-benzeneacetic acid (3-​endo)​-​8-​methyl-​8-​azabicyclo[3.2.1]​oct-​3-​yl ester sulfate, hydrate (2:1:1)
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Size
Estado
Price
Qty
1ml
A408832-1ml
2

106,90US$

154,90US$
Guardar 48,00 US$ (30.99%)
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Why this grade

10mM 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.

Descripción general

Information

Atropine sulfate monohydrate is a competitive antagonist for themuscarinic acetylcholine receptor, used to decrease the production of saliva and secretions of the airway prior to surgery.
In vitro

Atropine increases the release of the neurotransmitter dopamine into the superfusate in vitro at 100-500 mM and into the vitreous in vivo at 250 mg. Atropine induces spreading depression (SD) in the in vitro preparation. Atropine reduces the ERG b- and d-wave, leads to damped oscillations of RPE potentials, and reverses the ERG c-wave. Atropine suppresses myopia only at doses at which severe nonspecific side effects are observed in the retina.

In vivo

Atropine (1.0 mg/kg, i.p.), but not methylatropine (1.0 mg/kg, i.p.), prevents the enhancement of retention induced by both doses of the anticholinesterase when given immediately after training in mice. Atropine administration effectively prevents bradycardia and second-degree heart block but induces pulsus alternans and hypertension in dogs. Atropine has no effect on handling-induced acetylcholine output in the presence of 10 nM neostigmine, but causes greater and longer increases in the presence of 100 nM and 1000 nM neostigmine in rats. Atropine not only blocks the rapid eye movement (REM) sleep increases induced by CGS but it also tends to decrease REM sleep compared to atropine preceding saline in rats. Atropine decreases the time to exhaustion by 67% in intact rats and by 96.2% in adrenodemedullated (ADM) and also reduces the exercise-induced pituitary prolactin (PRL) release in both intact (50%) and ADM rats (90%).
Cell Data

cell lines:Rodent fibrosarcoma KHT cells

Concentrations:

Incubation Time:

Powder Purity:≥99%

Specifications

Sinónimos
α-​(hydroxymethyl)​-benzeneacetic acid (3-​endo)​-​8-​methyl-​8-​azabicyclo[3.2.1]​oct-​3-​yl ester sulfate, hydrate (2:1:1)
Especificaciones y pureza
10mM in DMSO
Mecanismos bioquímicos y fisiológicos
Atropine sulfate monohydrate is a competitive antagonist for the muscarinic acetylcholine receptor, used to decrease the production of saliva and secretions of the airway prior to surgery.
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Tipo de acción
ANTAGONIST
Nombres e identificadores
Isómeros SMILES CN1[C@@H]2CC[C@H]1CC(C2)OC(=O)C(CO)C3=CC=CC=C3.CN1[C@@H]2CC[C@H]1CC(C2)OC(=O)C(CO)C3=CC=CC=C3.O.OS(=O)(=O)O
WGK Alemania 2
Número ONU 1544
Peso molecular 694.83
Beilstein 6109275
Reaxy-Rn 25031488
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=25031488&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

Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
SolubilidadSolubility (25°C) In vitro 0.5MNAOH 3 mg/mL (10.07 mM); DMSO: 0 mg/mL (0.0 mM); Water: 0 mg/mL (0.0 mM);
Punto de fusión (°C)187°C
Citations of This Product
Referencias
1. Yi Xiao, Haomin Yi, Jingzhi Zhu, Suhua Chen, Guofang Wang, Yilong Liao, Yuanyuan Lei, Liyin Chen, Xingcai Zhang, Fangfu Ye.  (2022)  Evaluation of DNA adduct damage using G-quadruplex-based DNAzyme.  Bioactive Materials,      [PMID:36406255] [10.1016/j.bioactmat.2022.10.002]
2. Yazhou Qin, Yuanzhao Wu, Binjie Wang, Jiye Wang, Xingsen Zong, Weixuan Yao.  (2021)  Controllable preparation of sea urchin-like Au NPs as a SERS substrate for highly sensitive detection of the toxic atropine.  RSC Advances,  11  (32): (19813-19818).  [PMID:35479250] [10.1039/D1RA03223B]
3. Lisiqi Xie, Xiao Huang, Bin Su.  (2017)  Portable Sensor for the Detection of Choline and Its Derivatives Based on Silica Isoporous Membrane and Gellified Nanointerfaces.  ACS Sensors,      [PMID:28723110] [10.1021/acssensors.7b00166]
4. Jian-Jun Meng, Jia-Wei Shen, Guang Li, Chang-Jie Ouyang, Jia-Xi Hu, Zi-Shuo Li, Hang Zhao, Yi-Ming Shi, Mei Zhang, Rong Liu, Ju-Tao Chen, Yu-Qian Ma, Huan Zhao, Tian Xue.  (2023)  Light modulates glucose metabolism by a retina-hypothalamus-brown adipose tissue axis.  CELL,      [PMID:36669474] [10.1016/j.cell.2022.12.024]
5. Ying Miao, Huan Zhao, Yu-Fei Li, Yan-Ping Sun, Rui Bi, Hongli Li, Xin Fang, Zi-Shuo Li, Yu-Hua Ma, Long-Bao Lv, Kai An, Jian-Jun Meng, Yong-Gang Yao, Tian Xue.  (2025)  Light at night negatively affects mood in diurnal primate-like tree shrews via a visual pathway related to the perihabenular nucleus.  PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA,  122  (23): (e2411280122).  [PMID:40478874] [10.1073/pnas.2411280122]
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