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Merck

W353108

Sigma-Aldrich

环己烷羧酸

≥98%, FG

别名:

六氢苯甲酸

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About This Item

线性分子式:
C6H11CO2H
CAS号:
分子量:
128.17
FEMA编号:
3531
Beilstein:
970529
EC 号:
欧洲委员会编号:
11911
MDL编号:
UNSPSC代码:
12164502
PubChem化学物质编号:
Flavis编号:
8.060
NACRES:
NA.21

生物来源

synthetic

质量水平

等级

FG
Kosher

管理合规性

EU Regulation 1334/2008 & 872/2012
FDA 21 CFR 110

方案

≥98%

折射率

n20/D 1.461 (lit.)

沸点

232-233 °C (lit.)

mp

29-31 °C (lit.)

密度

1.033 g/mL at 25 °C (lit.)

应用

flavors and fragrances

文件

see Safety & Documentation for available documents

食品过敏原

no known allergens

性状检查

fruity; acidic

SMILES字符串

OC(=O)C1CCCCC1

InChI

1S/C7H12O2/c8-7(9)6-4-2-1-3-5-6/h6H,1-5H2,(H,8,9)

InChI key

NZNMSOFKMUBTKW-UHFFFAOYSA-N

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一般描述

Cyclohexanecarboxylic acid occurs naturally in the leaves of Ormosia henryi Prain.[1] It is also one of the aromatic volatile compounds found in the secretion of tail glands of red deer.[2]

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 2

储存分类代码

11 - Combustible Solids

WGK

WGK 2

闪点(°F)

230.0 °F - closed cup

闪点(°C)

110 °C - closed cup

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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A new sexual signal in rutting male red deer: Age related chemical scent constituents in the belly black spot.
Martin J, et al.
Mammalian Biology-Zeitschrift fur Saugetierkunde, 79(6), 362-368 (2014)
GC-MS Analysis of Chemical Constituents of the Volatile Oil from Leaves of Ormosia henryi Prain.
Jiexiong NBZWF & Mi T.
Guangdong Forestry Science and Technology, 2, 012-012 (2012)
Housna Mouttaki et al.
Environmental microbiology, 10(12), 3265-3274 (2008-08-19)
In methanogenic environments, the main fate of benzoate is its oxidization to acetate, H(2) and CO(2) by syntrophic associations of hydrogen-producing benzoate degraders and hydrogen-using methanogens. Here, we report the use of benzoate as an electron acceptor. Pure cultures of
Christo Christov et al.
ChemMedChem, 6(1), 131-140 (2010-12-07)
2-(3,5-Dichlorophenylcarbamoyl)cyclohexanecarboxylic acid (1) is a potent and selective positive allosteric modulator of metabotropic glutamate receptor subtype 4 (mGluR4). The activity of 1 was reported to reside in the cis diastereomer with equal potency between its enantiomeric forms (Niswender et al., Mol. Pharmacol.
P G Egland et al.
Journal of bacteriology, 177(22), 6545-6551 (1995-11-01)
The first step of anaerobic benzoate degradation is the formation of benzoyl-coenzyme A by benzoate-coenzyme A ligase. This enzyme, purified from Rhodopseudomonas palustris, is maximally active with 5 microM benzoate. To study the molecular basis for this reaction, the benzoate-coenzyme

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