12353
苯甲酸
reference material for titrimetry, certified by BAM, >99.5%
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线性分子式:
C6H5COOH
化学文摘社编号:
分子量:
122.12
NACRES:
NA.24
PubChem Substance ID:
eCl@ss:
39023903
UNSPSC Code:
41116107
EC Number:
200-618-2
MDL number:
Beilstein/REAXYS Number:
636131
产品名称
苯甲酸, reference material for titrimetry, certified by BAM, >99.5%
InChI key
WPYMKLBDIGXBTP-UHFFFAOYSA-N
InChI
1S/C7H6O2/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H,8,9)
SMILES string
OC(=O)c1ccccc1
grade
reference material
vapor density
4.21 (vs air)
vapor pressure
10 mmHg ( 132 °C)
assay
>99.5%
autoignition temp.
1061 °F
quality
certified by BAM
technique(s)
titration: suitable
bp
249 °C (lit.)
mp
121-125 °C (lit.)
solubility
water: soluble (2.9 g/l at 25 °C)
density
1.32 g/cm3 at 20 °C
application(s)
environmental
format
neat
Quality Level
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Analysis Note
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。
Application
其可作为标准物质，用于在碱量滴定中标定滴定溶液。
Features and Benefits
- 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）
General description
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。
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Irrit. 2 - STOT RE 1 Inhalation
target_organs
Lungs
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 1
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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
S Nacht et al.
Journal of the American Academy of Dermatology, 4(1), 31-37 (1981-01-01)
The transepidermal penetration and metabolic disposition of 14C-benzoyl peroxide were assessed in vitro (excised human skin) and in vivo (rhesus monkey). In vitro, the benzoyl peroxide penetrated into the skin, through the stratum corneum or the follicular openings, or both
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
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)
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.
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