苄胺

CAS: 100-46-9 货号: B661158 分子式: C7H9N 分子量: 107.15 Beilstein号: 741984 EC号: 202-854-1
有货
级别和纯度: 10mM in DMSO
储存条件
避光,充氩,-80℃储存
运输条件
特低温运输
★
规格
库存
价格
数量
1ml
B661158-1ml
现货 Stock Image
¥999.90
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为什么选择此级别

,适用于对基线干扰要求严格的色谱和分析工作流程。

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储存与运输

避光,充氩,-80℃储存。特低温运输 。请查阅批次 COA 获取详细规格。

📋

质量文档

SDS、COA、产品数据表及规格说明书均可下载。可通过批号查询获取批次 COA。

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文献证明

在色谱分析、有机合成和交叉偶联反应领域已被 69 篇同行评审文献引用。

概述

呈强碱性。对二氧化碳敏感。能与水、醇及醚等混溶。易溶于丙酮,溶于苯。有毒,致死量(兔,经口)250mg/kg。有腐蚀性。有催泪性。对人的皮肤及粘膜有刺激性。

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.

规格

规格或纯度
10mM in DMSO
英文名称
Benzylamine
储存条件
避光,充氩,-80℃储存
运输条件
特低温运输
名称和识别符
EC号
202-854-1
分子类型
小分子
Isomeric SMILES
C1=CC=C(C=C1)CN
UN Number
Packing Group
I
分子量
107.15
Beilstein号
741984
Reaxy-Rn
741984
Reaxys-RN link address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=741984&ln=

技术文档

📋 安全数据表 (SDS)

全面的危险、操作、储存及法规合规文件。

下载 SDS →

✅ 分析证书 (COA)

批次质量数据。输入批号以获取对应 COA。

查询 COA →

📊 产品数据表

产品规格和应用的快速参考摘要。

查看数据表 →

🔬 规格说明书

该级别的完整质量属性和验收标准。

查看规格说明 →

高级数据

化学和物理性质
溶解性
Miscible with water, ethanol, diethyl ether, acetone, benzene and chloroform.
敏感性
对光敏感,对空气敏感
折光率
1.544
闪点(℉)
149 °F
闪点(℃)
65 °C
沸点
184-185°C
熔点
10°C
安全和危险性(GHS)
象形图
GHS05,   GHS07
信号词
Danger
危险声明

H314: 造成严重的皮肤灼伤和眼睛损伤

H302: 吞食有害

H312: 皮肤接触有害

预防措施声明

P280: 戴防护手套/穿防护服/戴防护眼罩/戴防护面具。

P302+P352: 如皮肤沾染:用水充分清洗。

P321: 特殊处理(请参阅此标签上的...)。

P405: 密闭存放

P501: 将内容物/容器处理到。。。

P264: 处理后要彻底洗手。

P260: 不要吸入灰尘/烟雾/气体/雾/蒸汽/喷雾。

P270: 使用本产品时,请勿进食、饮水或吸烟。

P301+P330+P331: 如误吞咽:漱口。不要诱导呕吐。

P304+P340: 如误吸入:将人转移到空气新鲜处,保持呼吸舒适体位。

P363: 再次使用之前,请清洗受污染的衣物。

P362+P364: 脱掉沾污的衣服,清洗后方可重新使用。

P330: 漱口

P301+P317: 如果被吞咽:请寻求医疗帮助。

P305+P354+P338: 如果进入眼睛:立即用水冲洗几分钟。取下隐形眼镜(如果有的话),并且操作简单。继续冲洗。

P317: 寻求紧急医疗救助。

P302+P361+P354: 如果接触皮肤:立即脱掉所有被污染的衣服。立即用水冲洗几分钟。

P316: 立即寻求紧急医疗救助。

WGK Germany
1
RTECS
DP1488500
Class
8
Merck Index
1125
个人防护装备
Faceshields,full-face respirator (US),Gloves,Goggles,multi-purpose combination respirator cartridge (US),type ABEK (EN14387) respirator filter
质检证书(CoA,COO,BSE/TSE 和分析图谱)
C of A & Other Certificates(BSE/TSE, COO):
输入批号以搜索分析图谱:
技术文档和文章
卤代杂环与交叉偶联:从底物识别到成键路线的科研选型框架(含产品导航及表1–表5)
Haloheterocycles and Cross-Coupling: A Research-Oriented Selection Framework from Substrate Identification to Bond-Forming Routes (Including Product Navigation and Tables 1–5)
β-酰氧基烯基酰胺(AAAs):一种值得关注的酰胺键与肽键构建新思路
β-Acyloxy Alkenyl Amides (AAAs): A New Approach to Amide Bond and Peptide Bond Construction Worth Attention
DAST 介导的室温成酰胺反应:方法特点、应用价值与适用范围
DAST-Mediated Amidation at Room Temperature: Method Features, Practical Value, and Scope of Applicability
认识 ATD-DMAP:从试剂设计到成酯、成酰胺与手性保持
Understanding ATD-DMAP: From Reagent Design to Esterification, Amidation, and Stereochemical Integrity
TCFH–NMI 在高含水体系中的酰胺化:研究价值、方法认识与实验启示
TCFH–NMI Amidation in Highly Aqueous Media: Research Value, Methodological Understanding, and Experimental Insights
重新认识三甲基铝:未保护氨基酸一锅法肽链延长的方法设计与实验价值
Reassessing Trimethylaluminum: Method Design and Experimental Value of One-Pot Peptide Elongation from Unprotected Amino Acids
DSC 的方法学价值:NHS 型活化中间体的构建与选用判断
The Methodological Value of DSC: Building NHS-Type Activated Intermediates and Deciding When to Use Them
腈基如何构建:直接引入、前体脱水、氧化/脱氢与无氰工艺的路线判断
How to Construct Nitriles: Route Selection Across Direct Introduction, Precursor Dehydration, Oxidation/Dehydrogenation, and Cyanide-Free Processes
Boc₂O 的选用不能只看保护引入:从底物亲核性、介质效应到脱保护路径的实验判断
Boc₂O Selection Cannot Be Judged by Protection Installation Alone: Experimental Decision-Making from Substrate Nucleophilicity and Medium Effects to Deprotection Pathways
三光气在有机合成中的实验判断:按反应任务理解其选用逻辑
Experimental Evaluation of Triphosgene in Organic Synthesis: Understanding Its Selection Logic Through Reaction Tasks
三苯基膦参与的羧酸活化与酰胺键形成:活化路径、酸酐竞争与适用场景
Triphenylphosphine-Involved Carboxylic Acid Activation and Amide Bond Formation: Activation Pathways, Anhydride Competition, and Applicability Scenarios
ADMP 用于伯胺转有机叠氮化物的实验判断:底物亲核性、碱匹配与介质选择
Experimental Considerations for the Use of ADMP in the Conversion of Primary Amines to Organic Azides: Substrate Nucleophilicity, Base Matching, and Medium Selection
腰果壳油(CNSL):从腰果加工副产物到生物基涂料树脂反应型原料
Cashew Nut Shell Liquid (CNSL): From Cashew Processing By-Product to Reactive Bio-Based Raw Material for Coating Resins
CTSOBt 苯并三氮唑-磺酸酯缩合试剂:羧酸活化与合成应用价值
CTSOBt Benzotriazole–Sulfonate Coupling Reagent: Carboxylic Acid Activation and Synthetic Application Value
氮杂三环烷烃的张力释放:三维氮杂桥环的桥位模块化官能团化与立体控制
Strain Release of Azatricycloalkanes: Modular Bridge-Position Functionalization and Stereochemical Control of Three-Dimensional Bridged Aza Scaffolds
从光催化开环到骨架重构:氧杂环丁烷氧原子置换的反应逻辑与合成应用
From Photocatalytic Ring Opening to Skeletal Reconstruction: Reaction Logic and Synthetic Applications of Oxygen-Atom Replacement in Oxetanes
含水介质中酰胺化试剂的选择逻辑:竞争反应、活化中间体与底物效应
Logic for Selecting Amidation Reagents in Aqueous Media: Competing Reactions, Activated Intermediates, and Substrate Effects
一级、二级胺为何难以直接参与经典Mitsunobu反应:BEHT介导醇胺化的机理、构型翻转与反应范围
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
氮丙啶在药物合成中的构建与转化:环张力、N-取代调控、选择性开环与骨架扩展
Construction and Transformation of Aziridines in Drug Synthesis: Ring Strain, N-Substituent Control, Selective Ring Opening, and Scaffold Expansion
NH₄SCN的双重作用与CN转移:从SCN⁻电化学氧化到1-氰基咪唑并[1,5-a]吡啶构建
Dual Role of NH₄SCN and CN Transfer: From Electrochemical Oxidation of SCN⁻ to the Construction of 1-Cyanoimidazo[1,5-a]pyridines
从临时共价组装到分子内 Smiles 芳基迁移:DCPDC 介导的酚–伯胺 C–N 交叉偶联
From Temporary Covalent Assembly to Intramolecular Smiles Aryl Migration: DCPDC-Mediated Phenol–Primary Amine C–N Cross-Coupling
此产品的引用文献
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