Phenylguanidine carbonate salt - ≥99% , CAS No.14018-90-7

CAS: 14018-90-7 Cat. No.: P131885 Peso molecular: 135.17 (free carbonate basis) PubChem CID: 16217093
Disponible para pedir
GRADE & PURITY ≥99%
Synonyms
FT-0657392 | XDSYAIICRRZSJX-UHFFFAOYSA-N | benzyl-(2-chloro-ethyl)-methylamine hydrochloride | Carbonic acid, compound with phenylguanidine (1:1) | Phenylguanidine carbonate salt | 1-Phenylguanidine carbonate | MFCD03427114 | SY059286 | DTXSID70216974 | P
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5g
P131885-5g
3
13,90US$
25g
P131885-25g
2
17,90US$
100g
P131885-100g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
70,90US$
500g
P131885-500g
1
350,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal 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 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Product Application:
Reactant involved in synthesis of polo-like kinase 1 inhibitors Phenylguanidine carbonate salt may be used in the preparation of the following bioactive compounds: • (E)-methyl 2-(2-((6-cyclopropyl-2-(phenylamino)pyrimidin-4-yloxy)methyl)phenyl)-3-methoxyacrylate • cyprodinil • 5,6-dihydropyrido[2,3-d]pyrimidine • ethyl 1-methyl-8-(phenylamino)-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylate • 2-(phenylamino)-4-(trifluoromethyl)-1,6-dihydropyrimidine derivatives

Specifications

Sinónimos
FT-0657392 | XDSYAIICRRZSJX-UHFFFAOYSA-N | benzyl-(2-chloro-ethyl)-methylamine hydrochloride | Carbonic acid, compound with phenylguanidine (1:1) | Phenylguanidine carbonate salt | 1-Phenylguanidine carbonate | MFCD03427114 | SY059286 | DTXSID70216974 | P
Especificaciones y pureza
≥99%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Pureza
≥99%
Nombres e identificadores
Pubchem Sid488199215
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488199215
Sonrisas canónicasC1=CC=C(C=C1)N=C(N)N.C(=O)(O)O
IUPAC Namecarbonic acid;2-phenylguanidine
InChIKeyXDSYAIICRRZSJX-UHFFFAOYSA-N
INCHI1S/C7H9N3.CH2O3/c8-7(9)10-6-4-2-1-3-5-6;2-1(3)4/h1-5H,(H4,8,9,10);(H2,2,3,4)
Isómeros SMILES C1=CC=C(C=C1)N=C(N)N.C(=O)(O)O
WGK Alemania 3
PubChem CID 16217093
Peso molecular 135.17 (free carbonate basis)

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
SuperclassBenzenoids
ClaseBenzene and substituted derivatives
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentBenzene and substituted derivatives
Alternative Parents Organic carbonic acids  Guanidines  Propargyl-type 1,3-dipolar organic compounds  Organopnictogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkNot available
Substituents Monocyclic benzene moiety - Carbonic acid derivative - Carbonic acid - Guanidine - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

6 results found

Lot NumberCertificate TypeFechaArticulo
F2413036Certificate of AnalysisMar 18, 2026 P131885
G2517051Certificate of AnalysisJul 24, 2025 P131885
L2125162Certificate of AnalysisOct 07, 2023 P131885
L2125165Certificate of AnalysisOct 07, 2023 P131885
L2125396Certificate of AnalysisOct 07, 2023 P131885
L2125414Certificate of AnalysisOct 07, 2023 P131885
Propiedades químicas y físicas
Punto de fusión (°C)149-153 °C
Peso molecular197.190 g/mol
XLogP3
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count4
Rotatable Bond Count1
Exact Mass197.08 Da
Monoisotopic Mass197.08 Da
Topological Polar Surface Area122.000 Ų
Heavy Atom Count14
Formal Charge0
Complexity147.000
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 Count2
Citations of This Product
Referencias
1. Qiaocheng Feng, Mei Cui, Jingru Chen, Xueyi Zheng, Liangqia Guo.  (2024)  Enhanced long-term stability of stained microplastics with carbon nitride fluorescent polymer for tracking.  Environmental Technology & Innovation,      [PMID:] [10.1016/j.eti.2024.103593]
2. Jingru Chen, Xiaomin Zhang, Heng Lu, Yali Wu, Liangqia Guo.  (2025)  Hydroxyl and phenyl co-modified carbon nitride-based ratiometric fluorescent nanoprobe for monitoring mitochondrial pH in live cells and differentiating cell death.  TALANTA,      [PMID:40056646] [10.1016/j.talanta.2025.127843]
Calculadoras de soluciones
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