13365
N,N-二甲基苄胺
≥99.5% (GC)
别名:
N-苄基二甲胺, BDMA, DMBA
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线性分子式:
C6H5CH2N(CH3)2
化学文摘社编号:
分子量:
135.21
UNSPSC Code:
12352200
NACRES:
NA.26
PubChem Substance ID:
EC Number:
203-149-1
Beilstein/REAXYS Number:
1099620
MDL number:
Assay:
≥99.5% (GC)
InChI key
XXBDWLFCJWSEKW-UHFFFAOYSA-N
InChI
1S/C9H13N/c1-10(2)8-9-6-4-3-5-7-9/h3-7H,8H2,1-2H3
SMILES string
CN(C)Cc1ccccc1
assay
≥99.5% (GC)
refractive index
n20/D 1.501 (lit.), n20/D 1.502
bp
183-184 °C/765 mmHg (lit.)
mp
−75 °C (lit.)
solubility
H2O: soluble
density
0.9 g/mL at 25 °C (lit.)
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signalword
Danger
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
134.6 °F - closed cup
flash_point_c
57 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
新产品
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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
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
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
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
Guang-Rong Peh et al.
Organic & biomolecular chemistry, 7(10), 2110-2119 (2009-05-08)
The wide dissemination of catalytic protocols in academic and industrial laboratories is facilitated by the development of catalysts that are not only highly active but also user-friendly, stable to moisture, air and long term storage and easy to prepare on
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