779482
1-叠氮基-4-碘苯 溶液
0.5 M in tert-butyl methyl ether, ≥95% (HPLC)
别名:
4-Iodophenyl azide solution
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关于此项目
经验公式（希尔记法）:
C6H4IN3
化学文摘社编号:
分子量:
245.02
Beilstein:
1939309
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.22
方案
≥95% (HPLC)
表单
solution
浓度
0.5 M in tert-butyl methyl ether
杂质
≤2.0% water
储存温度
−20°C
SMILES字符串
Ic1ccc(cc1)N=[N+]=[N-]
InChI
1S/C6H4IN3/c7-5-1-3-6(4-2-5)9-10-8/h1-4H
InChI key
FJOKWWVZXVTOIR-UHFFFAOYSA-N
警示用语：
Danger
危险分类
Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT RE 1
储存分类代码
3 - Flammable liquids
WGK
WGK 3
闪点(°F)
-27.4 °F
闪点(°C)
-33 °C
法规信息
新产品
此项目有
M D Davison et al.
The Biochemical journal, 234(2), 413-420 (1986-03-01)
The hydrophobic photosensitive probe 1-azido-4-[125I]iodobenzene (AIB) partitioned preferentially into photoreceptor disc membranes and, upon u.v. irradiation, became covalently bound to opsin and phospholipid. The labelling of both protein and phospholipid was linearly related to AIB concentration. The amount of probe
M D Davison et al.
The Biochemical journal, 236(2), 389-395 (1986-06-01)
Opsin labelled with photoactivated 1-azido-4-[125I]iodobenzene was proteolysed in situ with Staphylococcus aureus V8 proteinase to yield two radioactive membrane-bound fragments. These were separated, cleaved with CNBr and the resultant peptides sequenced in order to locate the radiolabelled residues. In the
Labeling of hydrophobic polypeptides from the chick lens membrane.
L J Takemoto et al.
Experimental eye research, 35(5), 535-540 (1982-11-01)
M E Haw
British journal of anaesthesia, 53(6), 577-584 (1981-06-01)
Xenopus laevis tadpoles were produced from wild-caught, laboratory-reared toads. Separate sets were fed on diets of (1) liver powder; (2) nettle powder; (3) aminosol and Intralipid. The tadpoles were reared for 3 weeks at 22 degrees C and then three
E Wells et al.
The Biochemical journal, 187(3), 719-725 (1980-06-01)
To investigate the intramembranous domains of the major band-3 polypeptide, human erythrocyte membranes were labelled with 1-azido-4-[125I]iodobenzene. The anion-exchange protein has been isolated by a new procedure that decreases possible contamination by other integral membrane proteins of similar molecular weight.
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