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product name
硫酸96%, Suprapur®
等級
for inorganic trace analysis
品質等級
agency
suitable for EPA 300
蒸汽密度
<0.3 (25 °C, vs air)
蒸汽壓力
0.0001 hPa ( 20 °C)
1 mmHg ( 146 °C)
化驗
≥95% (acidimetric)
96%
形狀
liquid
pH值
0.3 (25 °C, 49 g/L in H2O)
bp
~290 °C (lit.)
mp
-20 °C
密度
1.840 g/mL at 25 °C (lit.)
負離子痕跡
chloride (Cl-): ≤100 ppb
nitrate (NO3-): ≤200 ppb
phosphate (PO43-): ≤100 ppb
正離子痕跡
Ag: ≤1.0 ppb
Al: ≤5.0 ppb
As: ≤0.5 ppb
Au: ≤0.5 ppb
Ba: ≤1.0 ppb
Be: ≤0.5 ppb
Bi: ≤0.5 ppb
Ca: ≤5.0 ppb
Cd: ≤1.0 ppb
Co: ≤0.5 ppb
Cr: ≤1.0 ppb
Cu: ≤0.5 ppb
Fe: ≤5.0 ppb
Ga: ≤0.5 ppb
Ge: ≤1.0 ppb
Hg: ≤2.0 ppb
In: ≤0.5 ppb
K: ≤2.0 ppb
Li: ≤0.5 ppb
Mg: ≤5.0 ppb
Mn: ≤0.5 ppb
Mo: ≤0.5 ppb
NH4+: ≤1.0 ppm
Na: ≤10.0 ppb
Ni: ≤2.0 ppb
Pb: ≤1.0 ppb
Pt: ≤0.5 ppb
Sb: ≤1.0 ppb
Se: ≤1.0 ppb
Sn: ≤1.0 ppb
Sr: ≤0.5 ppb
Ti: ≤1.0 ppb
Tl: ≤0.5 ppb
V: ≤0.5 ppb
Zn: ≤2.0 ppb
Zr: ≤0.5 ppb
SMILES 字串
OS(O)(=O)=O
儲存溫度
no temp limit
InChI
1S/H2O4S/c1-5(2,3)4/h(H2,1,2,3,4)
InChI 密鑰
QAOWNCQODCNURD-UHFFFAOYSA-N
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分析報告
颜色: ≤ 10 色度
氯化物(Cl): ≤ 100 ppb
硝酸盐 (NO₃): ≤ 200 ppb
磷酸盐(PO₄): ≤ 100 ppb
Ag(银): ≤ 1.0 ppb
Al(铝): ≤ 5.0 ppb
As(砷): ≤ 0.5 ppb
Au(金): ≤ 0.5 ppb
Ba(钡): ≤ 1.0 ppb
Be(铍): ≤ 0.5 ppb
Bi(铋): ≤ 0.5 ppb
Ca(钙): ≤ 5.0 ppb
Cd(镉): ≤ 1.0 ppb
Co(钴): ≤ 0.5 ppb
Cr(铬): ≤ 1.0 ppb
Cu(铜): ≤ 0.5 ppb
Fe(铁): ≤ 5.0 ppb
Ga(镓): ≤ 0.5 ppb
Ge(锗): ≤ 1.0 ppb
Hg(汞): ≤ 2.0 ppb
In(铟): ≤ 0.5 ppb
K(钾): ≤ 2.0 ppb
Li(锂): ≤ 0.5 ppb
Mg(镁) ≤ 5.0 ppb
Mn(锰): ≤ 0.5 ppb
Mo(钼): ≤ 0.5 ppb
NH₄(铵): ≤ 1.0 ppm
Na(钠): ≤ 10.0 ppb
Ni(镍): ≤ 2.0 ppb
Pb(铅): ≤ 1.0 ppb
Pt(铂): ≤ 0.5 ppb
Sr(锶): ≤ 1.0 ppb
Se(硒): ≤ 1.0 ppb
Sn(锡): ≤ 1.0 ppb
Sr(锶): ≤ 0.5 ppb
Ti(钛): ≤ 1.0 ppb
TI(铊): ≤ 0.5 ppb
V(钒): ≤ 0.5 ppb
Zn(锌): ≤ 2.0 ppb
Zr(锆): ≤ 0.5 ppb
可还原高锰酸钾的物质(SO₂形式): ≤ 2 ppm
灼烧残渣: ≤ 2 ppm
实际值在该浓度范围内会不可避免的受系统性
误差的影响。
法律資訊
訊號詞
Danger
危險聲明
危險分類
Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1A
儲存類別代碼
8A - Combustible, corrosive hazardous materials
水污染物質分類(WGK)
WGK 1
閃點(°F)
Not applicable
閃點(°C)
Not applicable
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商品
Control elemental impurities in drug products with analytical methods and materials to ensure patient safety.
Control elemental impurities in drug products with analytical methods and materials to ensure patient safety.
Control elemental impurities in drug products with analytical methods and materials to ensure patient safety.
Control elemental impurities in drug products with analytical methods and materials to ensure patient safety.
相关内容
This page is intended to make it easier to find the consumables you need based on the analytical method you’re using. Methods included on this page come from the EPA, Standard Methods and ASTM.
This page is intended to make it easier to find the consumables you need based on the analytical method you’re using. Methods included on this page come from the EPA, Standard Methods and ASTM.
This page is intended to make it easier to find the consumables you need based on the analytical method you’re using. Methods included on this page come from the EPA, Standard Methods and ASTM.
This page is intended to make it easier to find the consumables you need based on the analytical method you’re using. Methods included on this page come from the EPA, Standard Methods and ASTM.
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