28-4090
亜セレン酸ナトリウム
SAJ first grade, ≥90.0%
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この商品について
化学式:
Na2SeO3
CAS番号:
分子量:
172.94
UNSPSC Code:
12352302
PubChem Substance ID:
EC Number:
233-267-9
MDL number:
Assay:
≥90.0%
Grade:
SAJ first grade
Form:
powder
grade
SAJ first grade
vapor pressure
<0.00133 hPa ( 20 °C)
assay
≥90.0%
form
powder
availability
available only in Japan
mp
>350 °C (lit.)
SMILES string
[Na+].[Na+].[O-][Se]([O-])=O
InChI
1S/2Na.H2O3Se/c;;1-4(2)3/h;;(H2,1,2,3)/q2*+1;/p-2
InChI key
BVTBRVFYZUCAKH-UHFFFAOYSA-L
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signalword
Danger
Hazard Classifications
Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1
supp_hazards
保管分類
6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
毒物
pdsc
第一種指定化学物質
prtr
名称等を表示すべき危険物及び有害物
ishl_indicated
名称等を通知すべき危険物及び有害物
ishl_notified
28-4090-2-25G-J:4.548173009438E12
jan
Chih-Ching Yang et al.
PloS one, 9(7), e96006-e96006 (2014-07-02)
Deep-sea water (DSW), which is rich in micronutrients and minerals and with antioxidant and anti-inflammatory qualities, may be developed as marine drugs to provide intestinal protection against duodenal ulcers. We determined several characteristics in the modified DSW. We explored duodenal
D Pacitti et al.
Aquatic toxicology (Amsterdam, Netherlands), 130-131, 97-111 (2013-02-07)
Selenium (Se) is an oligonutrient with both essential biological functions and recognized harmful effects. As the selenocysteine (SeCys) amino acid, selenium is integrated in several Se-containing proteins (selenoproteins), many of which are fundamental for cell homeostasis. Nevertheless, selenium may exert
Ying Yi Chen et al.
Cancer chemotherapy and pharmacology, 74(1), 25-35 (2014-05-08)
SN 28049 is a new DNA-binding topoisomerase II poison identified by its curative activity against the murine colon 38 carcinoma. Previous studies showed activity to be associated with selective drug accumulation and retention in tumour tissue. Retention varied widely among