推薦產品
產品線
BioXtra
品質等級
化驗
≥98.0%
形狀
powder
雜質
≤0.0005% Phosphorus (P)
≤0.02% Insoluble matter
燃燒殘留物
≤0.1%
pH值
4.5-6.0 (25 °C, 114.1 g/L)
mp
131-135 °C (lit.)
溶解度
H2O: 1 M, clear, colorless
water: soluble 114.1 g/L at 20 °C
負離子痕跡
chloride (Cl-): ≤0.05%
正離子痕跡
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 字串
N.NS(O)(=O)=O
InChI
1S/H3NO3S.H3N/c1-5(2,3)4;/h(H3,1,2,3,4);1H3
InChI 密鑰
GEHMBYLTCISYNY-UHFFFAOYSA-N
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一般說明
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.
應用
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).
儲存類別代碼
13 - Non Combustible Solids
水污染物質分類(WGK)
WGK 1
閃點(°F)
Not applicable
閃點(°C)
Not applicable
分析證明 (COA)
輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號,寫有 ‘Lot’或‘Batch’.。
Chemistry of Pesticides., 262-262 (2012)
Flammability of polyamide 6 using the sulfamate system and organo-layered silicate.
Polymers For Advanced Technologies, 18(9), 737-745 (2007)
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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