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16139-18-7

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  • China Biggest Factory manufacturer supply AMINOGUANIDINE HYDROCHLORIDE CAS1937-19-5/1937-19-5 Annual 2000MT

    Cas No: 16139-18-7

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16139-18-7 Usage

Uses

Inhibitor (advanced glycosylation end-product formation).

Check Digit Verification of cas no

The CAS Registry Mumber 16139-18-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,3 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16139-18:
(7*1)+(6*6)+(5*1)+(4*3)+(3*9)+(2*1)+(1*8)=97
97 % 10 = 7
So 16139-18-7 is a valid CAS Registry Number.
InChI:InChI=1/CH6N4.ClH/c2-1(3)5-4;/h4H2,(H4,2,3,5);1H

16139-18-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name AMINOGUANIDINE HYDROCHLORIDE

1.2 Other means of identification

Product number -
Other names Aminoguanidine Chloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:16139-18-7 SDS

16139-18-7Related news

Synergistic anti-inflammatory interaction between meloxicam and AMINOGUANIDINE HYDROCHLORIDE (cas 16139-18-7) in carrageenan-induced acute inflammation in rats07/17/2019

Interaction studies with inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) inhibitor have been conducted to assess the nature of interaction and the possible therapeutic advantage. The interaction between meloxicam – a selective COX-2 inhibitor – and aminoguanidine hydrochlor...detailed

16139-18-7Relevant articles and documents

Green Energetic Nitrogen-Rich Salts of 1,1′-Dinitramino-5,5′-bistetrazolate

He, Piao,Wu, Le,Wu, Jinting,Wang, Qianyou,Li, Zhimin,Gozin, Michael,Zhang, Jianguo

, p. 11159 - 11168 (2017)

A series of nitrogen-rich energetic salts of 1,1′-dinitramino-5,5′-bistetrazolate (DNABT) guanidinium (1), aminoguanidinium (2), diaminoguanidinium (3), triaminoguanidinium (4), diaminouronium (5), 3,4-diamino-1,2,4-triazolium (6), and ethylenediammonium (7) was synthesized by a metathesis strategy and characterized by elemental analysis, mass spectrometry, and IR spectroscopy as well as single-crystal X-ray diffraction and differential scanning calorimetry (DSC). The natural bond orbitals (NBOs) and electrostatic potentials (ESPs) were further computed for a better understanding of the structures of the DNABT molecule. The heats of formation were calculated based on the Born–Haber energy cycle. The detonation parameters were evaluated by using the EXPLO5 program, and the sensitivities were measured according to BAM standers. These new salts exhibit highly positive heats of formation (407.0–1377.9 kJ mol?1) and good thermal stabilities (180–211 °C). Most of these compounds possess detonation velocities comparable to RDX and acceptable detonation pressures. The high volumes of explosion gases of the salts 3 and 4 (921 and 933 L kg?1, respectively) further support their power as explosives. The enhancing performances, the fact of being free of metals, and the more moderate sensitivities than K2DNABT, suggest that the salts 4 (D=8851 m s?1, P=29.0 GPa), 5 (D=9053 m s?1, P=32.3 GPa), and 6 (D=8835 m s?1, P=30.2 GPa) might be potential environmentally friendly energetic materials.

Thermodynamic and kinetic aspects of the reaction of aminoguanidine with malonic acid in acidic aqueous solutions

Chernysheva,Chernyshev,Korolenko,Taranushich

, p. 1813 - 1817 (2008)

Thermodynamic and kinetic features of the reaction of aminoguanidine with malonic acid in aqueous solutions at pH 0.5-1.3 to give mono-and diguanylhydrazides of malonic acid were examined, and the reaction mechanism was suggested.

PROCESS FOR STRAIGHTENING KERATIN FIBRES WITH A HEATING MEANS AND DENATURING AGENTS

-

, (2010/03/02)

The invention relates to a process for straightening keratin fibres, comprising: (i) a step in which a straightening composition containing at least two denaturing agents is applied to the keratin fibres, (ii) a step in which the temperature of the keratin fibres is raised, using a heating means, to a temperature of between 110 and 250° C.

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