402516
1H-吡唑-1-甲脒 盐酸盐
99%
别名:
1H-吡唑-1-甲脒盐酸盐, 吡唑-1-氨基亚胺 盐酸盐
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关于此项目
经验公式（希尔记法）:
C4H6N4 · HCl
化学文摘社编号:
分子量:
146.58
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
429-520-1
Beilstein/REAXYS Number:
5448758
MDL number:
产品名称
1H-吡唑-1-甲脒 盐酸盐, 99%
Quality Level
InChI key
RBZRMBCLZMEYEH-UHFFFAOYSA-N
InChI
1S/C4H6N4.ClH/c5-4(6)8-3-1-2-7-8;/h1-3H,(H3,5,6);1H
SMILES string
Cl[H].NC(=N)n1cccn1
assay
99%
form
powder
mp
167-170 °C (lit.)
functional group
amine
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Application
1H-吡唑-1-甲脒盐酸盐可用于以下研究：
- 胍基中空纤维膜的制备。
- 胺类的鸟苷酸化和肽合成。
- 双胍胆固醇衍生物的合成。
General description
1H-吡唑-1-甲酰脒盐酸盐为吡唑衍生物，为杂环化合物。在药物合成研究中应用广泛。吡唑环构成了各种非甾体抗炎药 (NSAIDs) 和抗高血压药物的主要核心。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Sens. 1 - STOT RE 2
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Hironori Izawa et al.
Biomolecules, 9(7) (2019-07-10)
In order to synthesize a promising material for developing a novel peptide/protein delivery system, guanidinylation of chitooligosaccharides with 1-amidinopyrazole hydrochloride was investigated herein. The production of guanidinylated chitooligosaccharides was demonstrated by infrared spectroscopy (IR), nuclear magnetic resonance (NMR), and elemental
Guanidinium-cholesterol cationic lipids: efficient vectors for the transfection of eukaryotic cells.
J P Vigneron et al.
Proceedings of the National Academy of Sciences of the United States of America, 93(18), 9682-9686 (1996-09-03)
Two cationic lipids, bis-guanidinium-spermidine-cholesterol (BGSC) and bis-guanidinium-trencholesterol (BGTC)-cholesterol derivatives bearing two guanidinium groups-have been synthesized and tested as artificial vectors for gene transfer. They combine the membrane compatible features of the cholesterol subunit and the favorable structural and high pKa
1H-Pyrazole-1-carboxamidine hydrochloride an attractive reagent for guanylation of amines and its application to peptide synthesis.
Bernatowicz MS, et al.
The Journal of Organic Chemistry, 57(8), 2497-2502 (1992)
Xiao Zhang et al.
ACS applied materials & interfaces, 12(14), 16088-16096 (2020-03-17)
Supramolecular hydrogels have great potential as biomaterials for tissue engineering applications or vehicles for delivering therapeutic agents. Herein, a self-healing and pro-osteogenic hydrogel system is developed based on the self-assembly of laponite nanosheets and guanidinylated chitosan, where laponite works as
Ekaterina K Ogurtsova et al.
Natural product communications, 10(7), 1171-1173 (2015-09-29)
The guanidine alkaloids, dihydropulchranin A (2), prepared from pulchranin A from the sponge Monanchora pulchra, and hexadecylguanidine (3), a synthetic analog of pulchranins, were studied for their TRPV channel-regulating activities. Compound 2 was active as an inhibitor of rTRPV1 and
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