AVAILABLE TO ORDER
GRADE & PURITY ≥98%(HPLC)
Synonyms
BCP28420 | Nu-Ranit | Zantac In Plastic Container | Ranibloc | SR-01000075288-2 | Wal-zan 75 | Zantic | HMS1568J03 | RANITIDINE HYDROCHLORIDE (EP MONOGRAPH) | HS-1000 | Ranitidine-Acid Reducer | ZANTAC 300 | Rani-Q | Ranitidine Tablet USP, 75mg | Zantac 1
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1g
R129213-1g
3

$10.90

$16.90
Save $6.00 (35.50%)
5g
R129213-5g
4

$25.90

$38.90
Save $13.00 (33.42%)
25g
R129213-25g
3

$88.90

$133.90
Save $45.00 (33.61%)
100g
R129213-100g
3

$180.90

$271.90
Save $91.00 (33.47%)
500g
R129213-500g
1

$600.90

$901.90
Save $301.00 (33.37%)
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Overview

A histamine H2-receptor antagonist.

Specifications

Synonyms
BCP28420 | Nu-Ranit | Zantac In Plastic Container | Ranibloc | SR-01000075288-2 | Wal-zan 75 | Zantic | HMS1568J03 | RANITIDINE HYDROCHLORIDE (EP MONOGRAPH) | HS-1000 | Ranitidine-Acid Reducer | ZANTAC 300 | Rani-Q | Ranitidine Tablet USP, 75mg | Zantac 1
Specifications & Purity
≥98%(HPLC)
Biochemical and Physiological Mechanisms
Ranitidine hydrochloride is a histamine H2-receptor antagonist used in the treatment of gastrointestinal lesions due to excessive gastric acid secretion.Potent, competitive and selective H 2 antagonist (pA 2 = 6.95 - 7.2). Inhibits gastric acid secretion
Storage
Store at 2-8°C, Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Note
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Purity
≥98%(HPLC)
Names and Identifiers
Pubchem Sid504762341
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504762341
Canonical SmilesCNC(=C[N+](=O)[O-])NCCSCC1=CC=C(O1)CN(C)C.Cl
IUPAC Name(E)-1-N'-[2-[[5-[(dimethylamino)methyl]furan-2-yl]methylsulfanyl]ethyl]-1-N-methyl-2-nitroethene-1,1-diamine;hydrochloride
InChIKeyGGWBHVILAJZWKJ-KJEVSKRMSA-N
INCHI1S/C13H22N4O3S.ClH/c1-14-13(9-17(18)19)15-6-7-21-10-12-5-4-11(20-12)8-16(2)3;/h4-5,9,14-15H,6-8,10H2,1-3H3;1H/b13-9+;
Isomeric SMILES CN/C(=C\[N+](=O)[O-])/NCCSCC1=CC=C(O1)CN(C)C.Cl
WGK Germany 2
RTECS KM6557000
Molecular Weight 350.86
Reaxy-Rn 5196014
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=5196014&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
SuperclassOrganic nitrogen compounds
ClassOrganonitrogen compounds
SubclassAmines
Intermediate Tree Nodes Not available
Direct ParentAralkylamines
Alternative Parents Furans  Heteroaromatic compounds  Trialkylamines  C-nitro compounds  Sulfenyl compounds  Dialkylamines  Dialkylthioethers  Propargyl-type 1,3-dipolar organic compounds  Oxacyclic compounds  Organic oxoazanium compounds  Hydrochlorides  Organic oxides  Hydrocarbon derivatives  Organic zwitterions  Organooxygen compounds  Organopnictogen compounds  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Aralkylamine - Heteroaromatic compound - Furan - Organic nitro compound - Tertiary amine - C-nitro compound - Tertiary aliphatic amine - Organic oxoazanium - Thioether - Oxacycle - Secondary amine - Secondary aliphatic amine - Organoheterocyclic compound - Dialkylthioether - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Sulfenyl compound - Organic oxygen compound - Organic zwitterion - Hydrochloride - Organosulfur compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as aralkylamines. These are alkylamines in which the alkyl group is substituted at one carbon atom by an aromatic hydrocarbyl group.
External Descriptors hydrochloride
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BLM Tchem Bloom syndrome protein (4248 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ATAD5 Tbio ATPase family AAA domain-containing protein 5 (122566 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MPHOSPH8 Tbio M-phase phosphoprotein 8 (656 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RAD52 Tchem DNA repair protein RAD52 homolog (856 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
ampC Beta-lactamase AmpC (62480 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Acinetobacter baumannii (41033 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cryptococcus neoformans (21258 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mapt Microtubule-associated protein tau (6 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
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.

11 results found

Lot NumberCertificate TypeDateItem
I2208175Certificate of AnalysisMar 11, 2026 R129213
I2208176Certificate of AnalysisMar 11, 2026 R129213
I2208177Certificate of AnalysisMar 11, 2026 R129213
I2208178Certificate of AnalysisMar 11, 2026 R129213
I2208204Certificate of AnalysisMar 11, 2026 R129213
D2422222Certificate of AnalysisFeb 05, 2026 R129213
G2001090Certificate of AnalysisNov 06, 2025 R129213
G2001089Certificate of AnalysisNov 06, 2025 R129213
D2422187Certificate of AnalysisMar 22, 2024 R129213
D2422188Certificate of AnalysisMar 22, 2024 R129213
G2001088Certificate of AnalysisMay 06, 2022 R129213

Show more ⌵

Chemical and Physical Properties
SolubilitySoluble in water (1.8 mg/mL), 45% (w/v) aq 2-hydroxypropyl-β-cyclodextrin (7.0 mg/mL), acetic acid, methanol, ethanol (<1 mg/mL), and DMSO (≥70 mg/mL). Insoluble in chloroform.
SensitivityAir & heat sensitive
Melt Point(°C)135 °C(dec.)
Molecular Weight350.870 g/mol
XLogP3
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count7
Rotatable Bond Count9
Exact Mass350.118 Da
Monoisotopic Mass350.118 Da
Topological Polar Surface Area112.000 Ų
Heavy Atom Count22
Formal Charge0
Complexity347.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count1
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds1
Covalently-Bonded Unit Count2
References
1. Zhizhuo Chai, Jingquan Wang, Yixue Dai, Erdeng Du, Hongguang Guo.  (2023)  Synergy between UV light and trichloroisocyanuric acid on methylisothiazolinone degradation: Performance, kinetics and degradation pathway..  ENVIRONMENTAL RESEARCH,      [PMID:37481058] [10.1016/j.envres.2023.116693]
2. Tao Long, Weiwei Tan, Xiangmin Tian, Zongjian Tang, Keming Hu, Liming Ge, Changdao Mu, Xinying Li, Yongbin Xu, Lei Zhao, Defu Li.  (2022)  Gelatin/alginate-based microspheres with sphere-in-capsule structure for spatiotemporal manipulative drug release in gastrointestinal tract.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:36521695] [10.1016/j.ijbiomac.2022.12.040]
3. Yangke Long, Jian Dai, Shiyin Zhao, Yiping Su, Zhongying Wang, Zuotai Zhang.  (2021)  Atomically Dispersed Cobalt Sites on Graphene as Efficient Periodate Activators for Selective Organic Pollutant Degradation.  ENVIRONMENTAL SCIENCE & TECHNOLOGY,      [PMID:33729757] [10.1021/acs.est.0c07794]
4. Fengyi Du, Yunchao Wu, Fengting Du, Lirong Zhang, Weiwei Feng, Lulu Zhao, Rong Cai, Lixia Xu, Gaorui Bian, Jiangang Li, Shengqiang Zou, Aihua Gong, Miaomiao Zhang.  (2019)  Construction of catechol-grafted chitosan alginate/barium sulfate microcapsules for computed tomography real-time imaging and gastroretentive drug delivery.  International Journal of Nanomedicine,      [PMID:31447554] [10.2147/IJN.S204237]
5. Yaqiong Guo, Yingying Xie, Jianhua Qin.  (2024)  A generic pump-free organ-on-a-chip platform for assessment of intestinal drug absorption.  Biotechnology Journal,  19  (2): (2300390).  [PMID:38375564] [10.1002/biot.202300390]
6. Zhang Mei, Zhao Jingwen, Long Yingying, Li Changsong, Yang Xiaoming.  (2024)  Carbon Dots Employed for the Detection of Ranitidine and Elaborating the Detecting Mechanism.  JOURNAL OF FLUORESCENCE,      [PMID:39269550] [10.1007/s10895-024-03912-5]
7. Yichong Wang, Danyan Li, Luqing Zhao, Jixiang Liu, Dan Dou, Nian Liu, Yudi Zhuo, Shengsheng Zhang.  (2025)  Mechanism of Yinxu Weitong Capsule in the treatment of precancerous lesions of gastric cancer based on network pharmacology and experimental validation.  JOURNAL OF ETHNOPHARMACOLOGY,      [PMID:39761837] [10.1016/j.jep.2024.119303]
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