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Merck
CN

191434

4-硝基苯甲胺 盐酸盐

97%

别名:

(4-Nitrophenyl)methanamine hydrochloride, 4-Nitrobenzenemethanamine hydrochloride, p-Nitrobenzylamine hydrochloride

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关于此项目

线性分子式:
O2NC6H4CH2NH2 · HCl
化学文摘社编号:
分子量:
188.61
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
242-441-3
Beilstein/REAXYS Number:
3629994
MDL number:
Assay:
97%
Form:
solid
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Quality Level

assay

97%

form

solid

mp

~265 °C (dec.) (lit.)

solubility

methanol:glacial acetic acid (1:1): soluble 25 mg/mL, clear, colorless to light yellow

functional group

amine, nitro

SMILES string

Cl.NCc1ccc(cc1)[N+]([O-])=O

InChI

1S/C7H8N2O2.ClH/c8-5-6-1-3-7(4-2-6)9(10)11;/h1-4H,5,8H2;1H

InChI key

SMIXZZMSWYOQPW-UHFFFAOYSA-N

Application

4-Nitrobenzylamine hydrochloride was used in chemical modification of graphite powder and multiwalled carbon nanotubes. It was also used in the preparation of 2-fluoro-6-(4-nitrohenzylamino)purine.


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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 Z Kirkel' et al.
Voprosy meditsinskoi khimii, 32(2), 118-125 (1986-03-01)
Oxidation of p-nitro- and p-dimethylaminomethyl derivatives of benzylamine, catalyzed by amine oxidases from human placenta and blood serum, was studied. The amine oxidase activity was estimated by means of a spectrophotometric procedure involving measurement of aldehyde formed during the reaction
Gregory G Wildgoose et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 6(2), 352-362 (2005-03-09)
We demonstrate that graphite powder and multiwalled carbon nanotubes (MWCNTs) can be derivatised by 4-nitrobenzylamine (4-NBA) simply by stirring the graphite powder or MWCNTs in a solution of acetonitrile containing 10 mM 4-NBA. We propose that 4-NBA partially intercalates at
Combinatorial synthesis of 2, 9-substituted purines.
Gray NS, et al.
Tetrahedron Letters, 38(7), 1161-1164 (1997)



全球贸易项目编号

货号GTIN
191434-25G04061838760203
191434-5G04061832098623