1-Hydroxybenzotriazole Monohydrate - ≥97% , CAS No.123333-53-9

CAS: 123333-53-9 Cat. No.: H106176 Peso molecular: 135.13 Beilstein Registry Number: 26,41 Número EC: 602-929-2
Disponible para pedir
GRADE & PURITY ≥97%
Synonyms
1-hydroxy-1H-1,2,3-benzotriazole hydrate | AM83834 | n-hydroxybenzotriazole h2o | 1,2,3-benzotriazole-1-ol, monohydrate | A805049 | HOBt hydrate wetted with not less than 20 wt. % water | N-Hydroxybenzotriazole.H2O | 1 -hydroxybenzotriazole hydrate | 1-Hy
Storage
Desiccated,Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
25g
H106176-25g
2

25,90US$

29,90US$
Guardar 4,00 US$ (13.38%)
100g
H106176-100g
1
62,90US$
500g
H106176-500g
5

176,90US$

205,90US$
Guardar 29,00 US$ (14.08%)
Enter a quantity for the sizes you want to add.
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Why this grade

≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Desiccated,Room temperature Ships Normal 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 88 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
1-hydroxy-1H-1, 2, 3-benzotriazole hydrate | AM83834 | n-hydroxybenzotriazole h2o | 1, 2, 3-benzotriazole-1-ol, monohydrate | A805049 | HOBt hydrate wetted with not less than 20 wt. % water | N-Hydroxybenzotriazole.H2O | 1 -hydroxybenzotriazole hydrate | 1-Hy
Especificaciones y pureza
≥97%
Mecanismos bioquímicos y fisiológicos
Inhibits racemization in peptide syntheses using DCC as condensing agent.
Condiciones de almacenamiento de almacenamiento
Desiccated, Room temperature
Enviado en
Normal
Pureza
≥97%
Nombres e identificadores
Pubchem Sid504762177
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504762177
Sonrisas canónicasC1=CC=C2C(=C1)N=NN2O.O
IUPAC Name1-hydroxybenzotriazole;hydrate
InChIKeyPJUPKRYGDFTMTM-UHFFFAOYSA-N
INCHI1S/C6H5N3O.H2O/c10-9-6-4-2-1-3-5(6)7-8-9;/h1-4,10H;1H2
Isómeros SMILES C1=CC=C2C(=C1)N=NN2O.O
CAS alternativo 80029-43-2
Peso molecular 135.13
Beilstein 26,41
Reaxy-Rn 5627231
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=5627231&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
SuperclassOrganoheterocyclic compounds
ClaseBenzotriazoles
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentBenzotriazoles
Alternative Parents Benzenoids  Triazoles  Heteroaromatic compounds  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Benzotriazole - Benzenoid - Heteroaromatic compound - 1,2,3-triazole - Triazole - Azole - Azacycle - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as benzotriazoles. These are organic compounds containing a benzene fused to a triazole ring (a five-membered ring with two carbon atoms and three nitrogen atoms).
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.

16 results found

Lot NumberCertificate TypeFechaArticulo
D2523113Certificate of AnalysisApr 10, 2024 H106176
D2523114Certificate of AnalysisApr 10, 2024 H106176
L2411486Certificate of AnalysisApr 10, 2024 H106176
L2411488Certificate of AnalysisApr 10, 2024 H106176
L2411508Certificate of AnalysisApr 10, 2024 H106176
K2307450Certificate of AnalysisOct 24, 2023 H106176
K2307453Certificate of AnalysisOct 24, 2023 H106176
K2307454Certificate of AnalysisOct 24, 2023 H106176
B2309452Certificate of AnalysisJan 05, 2023 H106176
B2309903Certificate of AnalysisJan 05, 2023 H106176
B2309951Certificate of AnalysisJan 05, 2023 H106176
E2429061Certificate of AnalysisJan 05, 2023 H106176
H2311040Certificate of AnalysisJan 05, 2023 H106176
B2226308Certificate of AnalysisDec 22, 2021 H106176
B2226325Certificate of AnalysisDec 22, 2021 H106176
B2226326Certificate of AnalysisDec 22, 2021 H106176

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Propiedades químicas y físicas
Sensibilidadlight sensitive
Punto de fusión (°C)160°C
Peso molecular153.140 g/mol
XLogP3
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count0
Exact Mass153.054 Da
Monoisotopic Mass153.054 Da
Topological Polar Surface Area51.900 Ų
Heavy Atom Count11
Formal Charge0
Complexity130.000
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
Preguntas frecuentes y artículos
From Analytical Instrument to Synthetic Platform: A New Strategy for Reconstructing Automated Flow Solid-Phase Peptide Synthesis with Standard Analytical HPLC
New Progress in the Solid-Phase Synthesis of Sterically Hindered Peptides: Background, Core Breakthroughs, and Implications for Automation Compatibility of the RMMR Strategy
TCFH–NMI Amidation in Highly Aqueous Media: Research Value, Methodological Understanding, and Experimental Insights
A New Balance in Coupling Reagents: How DMT-TU Balances Reactivity, Racemization Control, and Thermal Hazard
From “High Yield” to “Configuration Retention”: Activation-Stage Risks, Route Differences, and Selection Principles for Coupling Systems
The Methodological Value of HATU in Difficult Couplings: Reactivity Advantages, Stereochemical Retention, and Condition Management
Low-Racemization Control in Peptide Synthesis: An Inverse N→C Peptide Synthesis Strategy via Activated α-Aminoesters
Ynamide Coupling Reagents: From Low-Epimerization Activation Pathways to More Practically Usable N→C Inverse Peptide Synthesis
Decision Logic for Selecting Coupling Reagents in Amide Bond Formation: Activation Pathways, Side Reactions, Epimerization, Workup, and Safety
Experimental Assessment of HOPO in Carbodiimide-Mediated Amide Coupling: Low-Racemization Control, Application Scenarios, and Process Considerations
Experimental Judgment for CMPI in Carboxylic Acid Activation: Applicable Tasks, Base Matching, and Workup Burden
Experimental Judgment for TFPN in Carboxylic Acid Activation: Suitable Scenarios, Intermediate Distribution, and Nucleophile Compatibility
Citations of This Product
Referencias
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