Benzylamine - 10mM in DMSO , CAS No.100-46-9

CAS: 100-46-9 Cat. No.: B661158 分子式: C7H9N 分子量: 107.15 Beilstein Registry Number: 741984 EC番号: 202-854-1
注文可能
GRADE & PURITY 10mM in DMSO
Storage
Protected from light,Argon charged,Store at -80°C
Shipped In
Dry ice packs + Cold packs
★
Size
USA
ドイツ (EU)*
Price
Qty
1ml
B661158-1ml
受注生産 · 8~12週間

$285.90

$333.90
保存 $48.00 (14.38%)
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Protected from light,Argon charged,Store at -80°C Ships Dry ice packs + Cold packs 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 69 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

概要

Benzylamine undergoes oxidative deamination reaction catalyzed by benzylamine oxidase and monoamine oxidase type B.
Benzylamine was used in modification of alkanethiol monolayers via amide and ester formation reactions for attachment onto metal electrodes. It was used as carrier electrolyte for separation of alkali, alkaline earth and ammonium cations in water samples by capillary electrophoresis with indirect UV detection. It was used in synthesis of cross-linked porous copolymer supports based on N-(p-vinylbenzoyl)-2-methylalanine, styrene and divinylbenzene.

Specifications

仕様と純度
10mM in DMSO
保管条件
Protected from light,Argon charged,Store at -80°C
入荷
Dry ice packs + Cold packs
この製品は冷冷この冷このこの製品の運送が必要です。地上およびその他の経済サービスは利用できません。
名前と識別子
異性体SMILES
C1=CC=C(C=C1)CN
WGKドイツ
1
RTECS
DP1488500
UN番号
2735
包装グループ
I
分子量
107.15
Beilstein
741984
Reaxy-Rn
741984
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=741984&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

証明書(CoA、COO、BSE/TSEと分析図)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
化学的性質と物理的性質
溶解度Miscible with water, ethanol, diethyl ether, acetone, benzene and chloroform.
感度Light sensitive.air sensitive
屈折率1.544
引火点(°F)149 °F
引火点(°C)65 °C
沸点(°C)184-185°C
融点(°C)10°C
よくある質問と記事
Haloheterocycles and Cross-Coupling: A Research-Oriented Selection Framework from Substrate Identification to Bond-Forming Routes (Including Product Navigation and Tables 1–5)
β-Acyloxy Alkenyl Amides (AAAs): A New Approach to Amide Bond and Peptide Bond Construction Worth Attention
DAST-Mediated Amidation at Room Temperature: Method Features, Practical Value, and Scope of Applicability
Understanding ATD-DMAP: From Reagent Design to Esterification, Amidation, and Stereochemical Integrity
TCFH–NMI Amidation in Highly Aqueous Media: Research Value, Methodological Understanding, and Experimental Insights
Reassessing Trimethylaluminum: Method Design and Experimental Value of One-Pot Peptide Elongation from Unprotected Amino Acids
The Methodological Value of DSC: Building NHS-Type Activated Intermediates and Deciding When to Use Them
How to Construct Nitriles: Route Selection Across Direct Introduction, Precursor Dehydration, Oxidation/Dehydrogenation, and Cyanide-Free Processes
Boc₂O Selection Cannot Be Judged by Protection Installation Alone: Experimental Decision-Making from Substrate Nucleophilicity and Medium Effects to Deprotection Pathways
Experimental Evaluation of Triphosgene in Organic Synthesis: Understanding Its Selection Logic Through Reaction Tasks
Triphenylphosphine-Involved Carboxylic Acid Activation and Amide Bond Formation: Activation Pathways, Anhydride Competition, and Applicability Scenarios
Experimental Considerations for the Use of ADMP in the Conversion of Primary Amines to Organic Azides: Substrate Nucleophilicity, Base Matching, and Medium Selection
Cashew Nut Shell Liquid (CNSL): From Cashew Processing By-Product to Reactive Bio-Based Raw Material for Coating Resins
CTSOBt Benzotriazole–Sulfonate Coupling Reagent: Carboxylic Acid Activation and Synthetic Application Value
Strain Release of Azatricycloalkanes: Modular Bridge-Position Functionalization and Stereochemical Control of Three-Dimensional Bridged Aza Scaffolds
From Photocatalytic Ring Opening to Skeletal Reconstruction: Reaction Logic and Synthetic Applications of Oxygen-Atom Replacement in Oxetanes
Logic for Selecting Amidation Reagents in Aqueous Media: Competing Reactions, Activated Intermediates, and Substrate Effects
Why Primary and Secondary Amines Have Difficulty Participating Directly in the Classical Mitsunobu Reaction: Mechanism, Inversion of Configuration, and Reaction Scope of BEHT-Mediated Alcohol Amination
Construction and Transformation of Aziridines in Drug Synthesis: Ring Strain, N-Substituent Control, Selective Ring Opening, and Scaffold Expansion
Dual Role of NH₄SCN and CN Transfer: From Electrochemical Oxidation of SCN⁻ to the Construction of 1-Cyanoimidazo[1,5-a]pyridines
From Temporary Covalent Assembly to Intramolecular Smiles Aryl Migration: DCPDC-Mediated Phenol–Primary Amine C–N Cross-Coupling
Citations of This Product
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