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Merck

12353

Supelco

苯甲酸

reference material for titrimetry, certified by BAM, >99.5%

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25 G
$416.00

$416.00


预计发货时间2025年4月07日详情


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25 G
$416.00

About This Item

线性分子式:
C6H5COOH
CAS号:
分子量:
122.12
Beilstein:
636131
EC 号:
MDL编号:
UNSPSC代码:
41116107
eCl@ss:
39023903
PubChem化学物质编号:
NACRES:
NA.24

$416.00


预计发货时间2025年4月07日详情


获取大包装报价

等级

reference material

蒸汽密度

4.21 (vs air)

蒸汽压

10 mmHg ( 132 °C)

方案

>99.5%

自燃温度

1061 °F

质量

certified by BAM

技术

titration: suitable

沸点

249 °C (lit.)

mp

121-125 °C (lit.)

溶解性

water: soluble (2.9 g/l at 25 °C)

密度

1.32 g/cm3 at 20 °C

应用

environmental

包装形式

neat

SMILES字符串

OC(=O)c1ccccc1

InChI

1S/C7H6O2/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H,8,9)

InChI key

WPYMKLBDIGXBTP-UHFFFAOYSA-N

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一般描述

苯甲酸是在严格条件下以最高精度合格的容量法滴定标准品。采用容量中和法作为主要分析方法进行含量测定和同质性评估。

应用

其可作为标准物质,用于在碱量滴定中标定滴定溶液。

特点和优势

  • 以坚固玻璃瓶装固体形式提供,确保开封前整个保质期内的稳定性。
  • 可追溯至 NIST SRM
  • 高品质材料,可提供精准的滴定测定
  • 随附分析证书(CoA)

分析说明

精确浓度、有效期以及认证的详细信息请见每个包装内的证书和认证报告。含量和有效期见标签。

象形图

Health hazardCorrosion

警示用语:

Danger

危险声明

危险分类

Eye Dam. 1 - Skin Irrit. 2 - STOT RE 1 Inhalation

靶器官

Lungs

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 1

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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其他客户在看

Allen J Duplantier et al.
Journal of medicinal chemistry, 52(11), 3576-3585 (2009-05-15)
3-Hydroxyquinolin-2(1H)-one (2) was discovered by high throughput screening in a functional assay to be a potent inhibitor of human DAAO, and its binding affinity was confirmed in a Biacore assay. Cocrystallization of 2 with the human DAAO enzyme defined the
Copper-mediated C-H/C-H biaryl coupling of benzoic acid derivatives and 1,3-azoles.
Mayuko Nishino et al.
Angewandte Chemie (International ed. in English), 52(16), 4457-4461 (2013-03-21)
Ly Dieu Tran et al.
Journal of the American Chemical Society, 134(44), 18237-18240 (2012-10-30)
An auxiliary-assisted, copper catalyzed or promoted sulfenylation of benzoic acid derivative β-C-H bonds and benzylamine derivative γ-C-H bonds has been developed. The method employs disulfide reagents, copper(II) acetate, and DMSO solvent at 90-130 °C. Application of this methodology to the
Wanchun Xiang et al.
ChemSusChem, 6(2), 256-260 (2013-01-25)
Sensing the sun: Incorporation of a cyanomethyl benzoic acid electron acceptor into donor-π-acceptor sensitizers for dye-sensitized-solar cell is shown to lead to devices with improved conversion efficiency when compared with more widely used cyanoacetic acid acceptor.
G C Tremblay et al.
Pharmacology & therapeutics, 60(1), 63-90 (1993-10-01)
Detoxification of sodium benzoate by elimination as a conjugate with glycine, a nonessential amino acid, provides a pathway for the disposal of waste nitrogen. Since 1979, sodium benzoate has been widely used in the therapeutic regimen to combat ammonia toxicity

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