全部照片(1)
About This Item
經驗公式（希爾表示法）:
C9H9N3O2
CAS號碼:
分子量：:
191.19
Beilstein:
649044
EC號碼:
MDL號碼:
分類程式碼代碼:
41116107
PubChem物質ID:
推薦產品
等級
analytical standard
包裝
ampule of 100 mg
製造商／商標名
Chem Service, Inc. PS-1077
技術
HPLC: suitable
gas chromatography (GC): suitable
mp
>300 °C (lit.)
應用
cleaning products
cosmetics
food and beverages
personal care
格式
neat
SMILES 字串
COC(=O)Nc1nc2ccccc2[nH]1
InChI
1S/C9H9N3O2/c1-14-9(13)12-8-10-6-4-2-3-5-7(6)11-8/h2-5H,1H3,(H2,10,11,12,13)
InChI 密鑰
TWFZGCMQGLPBSX-UHFFFAOYSA-N
尋找類似的產品？ 前往 產品比較指南
應用
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
訊號詞
Danger
危險分類
Aquatic Acute 1 - Aquatic Chronic 1 - Muta. 1B - Repr. 1B - Skin Sens. 1
儲存類別代碼
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
客戶也查看了
Gonzalo Martínez-Fernández et al.
FEMS microbiology ecology, 91(8), fiv079-fiv079 (2015-07-18)
Study of the efficacy of methanogenesis inhibitors in the rumen has given inconsistent results, mainly due to poorly understood effects on the key microbial groups involved in pathways for methane (CH4) synthesis. The experiment described in this report was designed
Diego Forni et al.
BMC genomics, 16, 891-891 (2015-11-04)
Copy number variation (CNV) is a major component of genomic variation, yet methods to accurately type genomic CNV lag behind methods that type single nucleotide variation. High-throughput sequencing can contribute to these methods by using sequence read depth, which takes
Christoph Thalhammer et al.
Nephrology (Carlton, Vic.), 20(2), 91-95 (2014-10-28)
Haemodynamic stability of patients during haemodialysis (HD) sessions is of pivotal importance and accurate determination of dry weight remains a challenge. Little information is available about central venous and aortic pressure during dialysis. In this pilot study we used a
Przemyslaw Szafranski et al.
European journal of human genetics : EJHG, 23(2), 173-179 (2014-05-16)
Genomic copy-number variations (CNVs) constitute an important cause of epilepsies and other human neurological disorders. Recent advancement of technologies integrating genome-wide CNV mapping and sequencing is rapidly expanding the molecular field of pediatric neurodevelopmental disorders. In a previous study, a
Bin He et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(51), 18261-18266 (2014-12-10)
The androgen receptor (AR) is a key driver of prostate cancer (PC), even in the state of castration-resistant PC (CRPC) and frequently even after treatment with second-line hormonal therapies such as abiraterone and enzalutamide. The persistence of AR activity via
我們的科學家團隊在所有研究領域都有豐富的經驗，包括生命科學、材料科學、化學合成、色譜、分析等.
聯絡技術服務