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500 G
$67.06
1 KG
$101.00
3 KG
$319.00
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:
12352100
eCl@ss:
39023903
PubChem化学物质编号:
NACRES:
NA.21
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蒸汽密度
4.21 (vs air)
质量水平
蒸汽压
10 mmHg ( 132 °C)
产品线
ReagentPlus®
方案
99%
表单
crystalline
自燃温度
1061 °F
包装
poly bottle of 500 g
沸点
249 °C (lit.)
mp
121-125 °C (lit.)
溶解性
water: soluble 2.9 g/L at 25 °C
官能团
carboxylic acid
phenyl
储存温度
room temp
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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相关类别
一般描述
Benzoic acid is an organic aromatic monocarboxylic acid. It reacts with hydrogenating reagents to afford hexahydrobenzoic acid. On decomposition (by heating) in the presence of lime or alkali, it affords benzene and carbon dioxide. It can be synthesized by the cobalt or manganese catalyzed atmospheric oxidation of toluene.[1]
应用
Benzoic acid may be employed as a standard in the quantitative and calorimetric studies. It may be employed as an intermediate in the following syntheses:[1]
- paints
- pigments
- varnish
- wetting agents
- aroma compounds
- benzoyl chloride
- benzotrichloride
法律信息
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
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
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
其他客户在看
Eagleson M.
Concise Encyclopedia Chemistry, 122-122 (1994)
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
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.
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
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