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About This Item
线性分子式:
C6H5CH2N(CH3)2
CAS号:
分子量:
135.21
Beilstein:
1099620
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
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化驗
98%
折射率
n20/D 1.501 (lit.)
bp
183-184 °C/765 mmHg (lit.)
mp
−75 °C (lit.)
密度
0.9 g/mL at 25 °C (lit.)
SMILES 字串
CN(C)Cc1ccccc1
InChI
1S/C9H13N/c1-10(2)8-9-6-4-3-5-7-9/h3-7H,8H2,1-2H3
InChI 密鑰
XXBDWLFCJWSEKW-UHFFFAOYSA-N
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说明
价格
訊號詞
Danger
危險分類
Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B
儲存類別代碼
3 - Flammable liquids
水污染物質分類（WGK）
WGK 2
閃點（°F）
134.6 °F - closed cup
閃點（°C）
57 °C - closed cup
個人防護裝備
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
B Ballantyne et al.
Drug and chemical toxicology, 8(1-2), 43-56 (1985-01-01)
N-Benzyl-N,N-dimethylamine (BDMA), a polyester foam catalyst, was determined to have LD50 values of 0.65 (0.48-0.88) ml/kg perorally in the rat, and 1.66 (1.35-2.04) ml/kg by 24-hr occluded dermal contact in rabbits. The Lt50 for saturated vapor atmosphere exposure of rats
N Hayashi et al.
Organic letters, 3(14), 2249-2252 (2001-07-07)
[structure: see text] Three additional NMR databases, 1-3, in a chiral solvent are presented. The C.21-C.38 portion of oasomycin A is used to demonstrate the scope and limitation of the universal NMR database approach in a chiral solvent for assignment
B Ståhlbom et al.
International archives of occupational and environmental health, 70(6), 393-398 (1997-01-01)
The aim of the present study was to develop a method for generation of dimethylbenzylamine (DMBA) atmospheres in an exposure chamber and to investigate the possibility of using urinary DMBA metabolites for biological monitoring of exposure to DMBA. A DMBA
M A Patrauchan et al.
Journal of applied microbiology, 94(2), 266-272 (2003-01-22)
The aim of this work was to study the biodegradation of benzyldimethylalkylammonium chloride (BAC) by Aeromonas hydrophila sp. K, an organism isolated from polluted soil and capable of utilizing BAC as sole source of carbon and energy. High performance liquid
Y Kobayashi et al.
Organic letters, 3(14), 2253-2255 (2001-07-07)
[structure: see text] Examples of (13)C NMR desymmetrization of meso compounds are presented. On analysis of the NMR profiles of 1,3-diols, the additivity is recognized to predict the NMR profiles of 1,3,5-tirols.
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