추천 제품
제품 라인
BioXtra
Quality Level
분석
≥98.0%
양식
powder
불순물
≤0.0005% Phosphorus (P)
≤0.02% Insoluble matter
무기 잔류물
≤0.1%
pH
4.5-6.0 (25 °C, 114.1 g/L)
mp
131-135 °C (lit.)
solubility
H2O: 1 M, clear, colorless
water: soluble 114.1 g/L at 20 °C
음이온 미량물
chloride (Cl-): ≤0.05%
양이온 미량물
Al: ≤0.0005%
Ca: ≤0.0005%
Cu: ≤0.0005%
Fe: ≤0.0005%
K: ≤0.005%
Mg: ≤0.0005%
Na: ≤0.005%
Pb: ≤0.001%
Zn: ≤0.0005%
SMILES string
N.NS(O)(=O)=O
InChI
1S/H3NO3S.H3N/c1-5(2,3)4;/h(H3,1,2,3,4);1H3
InChI key
GEHMBYLTCISYNY-UHFFFAOYSA-N
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일반 설명
Ammonium sulfamate (AS) is ammonium salt containing sulfur. It acts as a flame retardant for polyamide 6 (PA6). AS can be prepared by neutralizing sulfamic acid with ammonia. AS is a hygroscopic compound that undergoes decomposition in the soil to form ammonium sulfate. It also shows herbicidal properties.
애플리케이션
Ammonium sulfamate may be used to remove unreacted nitrite during quantification of ceftazidime (CFZM) in either pure form or in pharmaceutical preparations by spectrophotometric method. It may be used in the preparation of ammonium dinitramide (ADN).
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 1
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
가장 최신 버전 중 하나를 선택하세요:
시험 성적서(COA)
Flammability of polyamide 6 using the sulfamate system and organo-layered silicate.
Polymers For Advanced Technologies, 18(9), 737-745 (2007)
Chemistry of Pesticides., 262-262 (2012)
Synthesis of Ammonium Dinitramide by Nitration of Potassium and Ammonium Sulfamate. The Effect of Sulfamate Conterion on ADN Purity.
Iranian Journal of Chemistry and Chemical Engineering, 27(1), 85-89 (2008)
The Plant cell, 32(12), 3921-3938 (2020-10-23)
Aluminum (Al) is a primary constraint for crop production on acid soils, which make up more than 30% of the arable land in the world. Al resistance in Arabidopsis (Arabidopsis thaliana) is achieved by malate secretion mediated by the Al-ACTIVATED
Acta pharmaceutica (Zagreb, Croatia), 58(3), 275-285 (2008-12-24)
Two spectrophotometric methods for the determination of ceftazidime (CFZM) in either pure form or in its pharmaceutical formulations are described. The first method is based on the reaction of 3-methylbenzothiazolin-2-one hydrazone (MBTH) with ceftazidime in the presence of ferric chloride
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