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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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.
Shuji Yasuike et al.
Chemical & pharmaceutical bulletin, 50(10), 1404-1406 (2002-10-10)
Novel, enantiomerically pure organoantimony compounds having a C-chiral amine moiety, (S)-(alpha-methyl-2-di-p-tolylstibanobenzyl)dimethylamine [AMSb] (2) and its (eta(6)-arene)chromium complex [AMSb-Cr(CO)(3)] (4), were prepared from common (S)-(alpha-methylbenzyl)dimethylamine (1) via its ortho-lithiated intermediates in short steps. The catalytic activity and enantioselectivity of the ligands
[Optimization of biomimetic oxidation reactions achieved with the aid of an iodosylbenzene and meso-tetraphenylporphinatoiron (III): application to antergan].
F Pautet et al.
Pharmaceutica acta Helvetiae, 63(4-5), 140-144 (1988-01-01)
[Thin-layer chromatographic method for determination of N,N-dimethylbenzilamine in the air during sanitary and chemical studies of polymers].
L P Novitskaia et al.
Gigiena i sanitariia, (11)(11), 63-64 (1993-11-01)
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
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