Atropine sulfate monohydrate - ≥98.5% , CAS No.5908-99-6

CAS: 5908-99-6 Cat. No.: A109524 Molecular Weight: 694.83 Beilstein Registry Number: 6109275 EC Number: 611-792-8
AVAILABLE TO ORDER
GRADE & PURITY ≥98.5%
Synonyms
Atropine sulfate hydrate | Benzeneacetic acid, .alpha.-(hydroxymethyl)-, (3-endo)-8-methyl-8-azabicyclo[3.2.1]oct-3-yl ester, sulfate, hydrate (2:1:1) (salt) | Atropine sulfate (JP17/USP) | 03J5ZE7KA5 | 1alphaH,5alphaH-Tropan-3alpha-ol (+-)-tropate (ester
Storage
Store at 2-8°C
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1g
A109524-1g
5
$13.90
5g
A109524-5g
5
$41.90
25g
A109524-25g
3
$127.90
100g
A109524-100g
2
$327.90
Enter a quantity for the sizes you want to add.
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Why this grade

≥98.5% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice 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.

📚

Literature proof

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

Overview

Atropine sulfate monohydrate is a broad-spectrum and competitive muscarinic acetylcholine receptor (mAChR) antagonist with anti-myopia effect.

Specifications

Synonyms
Atropine sulfate hydrate | Benzeneacetic acid, .alpha.-(hydroxymethyl)-, (3-endo)-8-methyl-8-azabicyclo[3.2.1]oct-3-yl ester, sulfate, hydrate (2:1:1) (salt) | Atropine sulfate (JP17/USP) | 03J5ZE7KA5 | 1alphaH, 5alphaH-Tropan-3alpha-ol (+-)-tropate (ester
Specifications & Purity
≥98.5%
Storage
Store at 2-8°C
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥98.5%
Names and Identifiers
Pubchem Sid488190997
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488190997
Canonical SmilesCN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3.CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3.O.OS(=O)(=O)O
IUPAC Name[(1R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl] 3-hydroxy-2-phenylpropanoate;sulfuric acid;hydrate
InChIKeyJPKKQJKQTPNWTR-BRYCGAMXSA-N
INCHI1S/2C17H23NO3.H2O4S.H2O/c2*1-18-13-7-8-14(18)10-15(9-13)21-17(20)16(11-19)12-5-3-2-4-6-12;1-5(2,3)4;/h2*2-6,13-16,19H,7-11H2,1H3;(H2,1,2,3,4);1H2/t2*13-,14+,15?,16?;;
Isomeric 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 Germany 2
UN Number 1544
Molecular Weight 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

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassAlkaloids and derivatives
ClassTropane alkaloids
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentTropane alkaloids
Alternative Parents Beta hydroxy acids and derivatives  Piperidines  Organic sulfuric acids  N-alkylpyrrolidines  Benzene and substituted derivatives  Trialkylamines  Carboxylic acid esters  Amino acids and derivatives  Monocarboxylic acids and derivatives  Azacyclic compounds  Primary alcohols  Organopnictogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkNot available
Substituents Tropane alkaloid - Beta-hydroxy acid - Sulfuric acid - Monocyclic benzene moiety - Hydroxy acid - Piperidine - N-alkylpyrrolidine - Benzenoid - Pyrrolidine - Organic sulfuric acid or derivatives - Tertiary aliphatic amine - Tertiary amine - Amino acid or derivatives - Carboxylic acid ester - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Organic oxide - Organic oxygen compound - Organonitrogen compound - Amine - Organooxygen compound - Primary alcohol - Carbonyl group - Organic nitrogen compound - Alcohol - Organopnictogen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as tropane alkaloids. These are organic compounds containing the nitrogenous bicyclic alkaloid parent N-Methyl-8-azabicyclo[3.2.1]octane.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

13 results found

Lot NumberCertificate TypeDateItem
C2204081Certificate of AnalysisDec 12, 2025 A109524
C2204105Certificate of AnalysisDec 12, 2025 A109524
I2111034Certificate of AnalysisJun 09, 2025 A109524
I2111035Certificate of AnalysisJun 09, 2025 A109524
I2111059Certificate of AnalysisJun 09, 2025 A109524
D2326067Certificate of AnalysisFeb 17, 2023 A109524
D2326068Certificate of AnalysisFeb 17, 2023 A109524
D2326072Certificate of AnalysisFeb 17, 2023 A109524
D2326075Certificate of AnalysisFeb 17, 2023 A109524
B2325332Certificate of AnalysisJan 25, 2022 A109524
B2325333Certificate of AnalysisJan 25, 2022 A109524
C2204116Certificate of AnalysisJan 25, 2022 A109524
B2325334Certificate of AnalysisAug 02, 2021 A109524

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Chemical and Physical Properties
SolubilitySoluble in water (2500 mg/ml) at 4°C, ethanol (200 mg/ml) at 4°C, Glycerol (400 mg/ml), and methanol.
SensitivityLight sensitive.
Melt Point(°C)187°C
Molecular Weight694.800 g/mol
XLogP3
Hydrogen Bond Donor Count5
Hydrogen Bond Acceptor Count13
Rotatable Bond Count10
Exact Mass694.314 Da
Monoisotopic Mass694.314 Da
Topological Polar Surface Area184.000 Ų
Heavy Atom Count48
Formal Charge0
Complexity434.000
Isotope Atom Count0
Defined Atom Stereocenter Count4
Undefined Atom Stereocenter Count2
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count4
Citations of This Product
References
1. 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]
2. 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]
3. 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]
4. 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]
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]
Solution Calculators
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