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Zaltidine - ≥98% , CAS No.85604-00-8

CAS: 85604-00-8 Cat. No.: Z127855 Molecular Weight: 222.27 PubChem CID: 56051
COA
Zaltidine - ≥98% CAS No(85604-00-8) by Aladdin Scientific
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
(4-(2-METHYLIMIDAZOL-5-YL)-2-THIAZOLYL)QUANIDINE | 85604-00-8 (free base) | A914628 | F84942 | GUANIDINE, (4-(2-METHYL-1H-IMIDAZOL-5-YL)-2-THIAZOLYL)- | GIMNAEMRNXUAQP-UHFFFAOYSA-N | Zaltidina [Spanish] | 1-(4-(2-methyl-1H-imidazol-4-yl)thiazol-2-yl)guani
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
★
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
5mg
Z127855-5mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$479.90
10mg
Z127855-10mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$799.90
50mg
Z127855-50mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$2,399.90
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SDS
Safety data
COA
Certificate
DS
Datasheet
SP
Spec sheet
Specifications Names and Identifiers Documentation Advanced Data Taxonomic Classification 3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solution Calculators Reviews
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

Quality documents

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

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
(4-(2-METHYLIMIDAZOL-5-YL)-2-THIAZOLYL)QUANIDINE | 85604-00-8 (free base) | A914628 | F84942 | GUANIDINE, (4-(2-METHYL-1H-IMIDAZOL-5-YL)-2-THIAZOLYL)- | GIMNAEMRNXUAQP-UHFFFAOYSA-N | Zaltidina [Spanish] | 1-(4-(2-methyl-1H-imidazol-4-yl)thiazol-2-yl)guani
Specifications & Purity
≥98%
Biochemical and Physiological Mechanisms

Description:
IC50 Value: N/A
Zaltidine is a H2-receptor antagonist, which has the antisecretory action.
in vitro: N/A
in vivo: In eight healthy male volunteers single oral doses of 5 mg, 25 mg and 100 mg produced dose-

Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥98%
Names and Identifiers
Canonical SmilesCC1=NC=C(N1)C2=CSC(=N2)N=C(N)N
IUPAC Name2-[4-(2-methyl-1H-imidazol-5-yl)-1,3-thiazol-2-yl]guanidine
InChIKeyGIMNAEMRNXUAQP-UHFFFAOYSA-N
INCHI1S/C8H10N6S/c1-4-11-2-5(12-4)6-3-15-8(13-6)14-7(9)10/h2-3H,1H3,(H,11,12)(H4,9,10,13,14)
Isomeric SMILES CC1=NC=C(N1)C2=CSC(=N2)N=C(N)N
PubChem CID 56051
Molecular Weight 222.27

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
SuperclassOrganoheterocyclic compounds
ClassAzoles
SubclassThiazoles
Intermediate Tree Nodes Not available
Direct Parent2,4-disubstituted thiazoles
Alternative Parents Imidazoles  Heteroaromatic compounds  Guanidines  Propargyl-type 1,3-dipolar organic compounds  Azacyclic compounds  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents 2,4-disubstituted 1,3-thiazole - Heteroaromatic compound - Imidazole - Guanidine - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as 2,4-disubstituted thiazoles. These are compounds containing a thiazole ring substituted at the positions 2 and 3.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
HRH2 Tclin Histamine H2 receptor (5428 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Canis familiaris (36305 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 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:
Chemical and Physical Properties
SolubilityDMSO
Molecular Weight222.270 g/mol
XLogP30.000
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count4
Rotatable Bond Count2
Exact Mass222.069 Da
Monoisotopic Mass222.069 Da
Topological Polar Surface Area134.000 Ų
Heavy Atom Count15
Formal Charge0
Complexity254.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Solution Calculators
Reviews

Customer Reviews

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