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標(biāo)準(zhǔn)品/甲醇中4種藥物混標(biāo)/BJS 201701

標(biāo)準(zhǔn)品/甲醇中4種藥物混標(biāo)/BJS 201701

價(jià)格 20
包裝 1
最小起訂量 1mL
更新日期 2024-12-13

產(chǎn)品詳情

中文名稱:標(biāo)準(zhǔn)品/甲醇中4種藥物混標(biāo)/BJS 201701品牌: TMstandard
貨期: 現(xiàn)貨庫(kù)存: ≥6
編號(hào): 81810a過(guò)期日期: 2025-01-04
2024-12-13 標(biāo)準(zhǔn)品/甲醇中4種藥物混標(biāo)/BJS 201701 1/20RMB 20 TMstandard
標(biāo)準(zhǔn)值100μg/mL

甲醇中4種藥物混標(biāo)

CAS號(hào) 名稱 標(biāo)準(zhǔn)值 單位
58-94-6 氯噻嗪 100 μg/mL
58-93-5 氫氯噻嗪 100 μg/mL
81131-70-6 普伐他汀鈉 100 μg/mL
54-31-9 呋塞米 100 μg/mL

Reference Material

This certificate is designed in accordance with ISO 17034 and ISO Guide 31. This reference material (RM) was designed,produced and verified in accordance with ISO/IEC 17025, ISO 17034 and a registered quality management system ISO 9001.

Product Name(產(chǎn)品名稱) 4 Drug Mix in Methanol,100μg/mL(甲醇中4種藥物混標(biāo))
Part Number(產(chǎn)品編號(hào)) 81810a
Lot Number(產(chǎn)品批號(hào)) -
Expiry Date(失效日期) 2026-Apr-02________________________
Storage(存儲(chǔ)條件) ??????????(2-8)℃
????????????????????????????????????????????????????????冷藏(2~8)℃
Transportation(運(yùn)輸條件) ????????Normal temperature transportation
?????????????????? ???????????????????????????????????????????(常溫運(yùn)輸)
CERTIFIED
Component
No.
(組分?jǐn)?shù))
Peak
Sequence
(出峰順序)
Component
(組分)
CAS No. Concentration
(μg/mL)
(濃度)
Relative Expanded
Uncertainty(%) (k=2)
(相對(duì)擴(kuò)展不確定度)
1 1 Chlorothiazide (氯噻嗪) 58-94-6 100 3
2 2 Hydrochlorothiazide (氫氯噻嗪) 58-93-5 100 3
3 3 Pravastatin Sodium1 (普伐他汀鈉) 81131-70-6 100 3
4 4 Furosemide (呋塞米) 54-31-9 100 3
Instrument(檢測(cè)儀器)
??HPLC/DAD
Column(色譜柱)
??C18(3.0x100mm,1.8μm)
Column Oven(柱溫)
??35℃
Wavelength(波長(zhǎng))
??230nm
Method Details(方法參數(shù))

??A:0.1% Phosphoric Acid(0.1% 磷酸)
??B:Acetonitrile(乙腈)
Time/min A/% B/%
0.00 90 10
0.50 90 10
4.00 10 90
8.00 10 90
8.10 90 10
Note

1.The?standard?value?of?pravastatin sodium?is??pravastatin.(普伐他汀鈉的標(biāo)準(zhǔn)值以普伐他汀計(jì))

Intended Use

This RM is intended for use in a laboratory as a calibration and quality control standard or in method development for analytical techniques.

Uncertainty

The certified value(s) and uncertainty(ies) are determined in accordance with ISO 17034 with an 95% confidence level (k=2). Uncertainty is based on the Total Combined Uncertainty, including uncertainties of preparation, purity of neat materials, homogeneity, stability testing.

Traceability

The balances used for gravimetric measurements are calibrated with weights traceable to the national standards. The calibration of the balances is verified annually by an external accredited calibration service. This analysis method has been verified using an approach consistent with ISO 17034:2016 & ISO 17025:2017.

Homogeneity

Random replicate samples of the final packaged RM have been analysed to prove homogeneity consistent with ISO 17034.

Storage

The RM should be stored in the original sealed bottle at the indicated temperature.

CERTIFICATE????ON QC????SIGNATURE
- RM Release

相關(guān)產(chǎn)品信息
編號(hào)產(chǎn)品名CAS規(guī)格品牌價(jià)格過(guò)期時(shí)間
81810a標(biāo)準(zhǔn)品/甲醇中4種藥物混標(biāo)/BJS 2017011mLTMstandard4002026-04-02
81810a標(biāo)準(zhǔn)品/甲醇中4種藥物混標(biāo)/BJS 2017011mLTMstandard202025-01-04
關(guān)鍵字: 標(biāo)準(zhǔn)品/甲醇中4種藥物混標(biāo)/BJS 201701;標(biāo)準(zhǔn)品/甲醇中4種藥物混標(biāo)/BJS 201701價(jià)格;標(biāo)準(zhǔn)品/甲醇中4種藥物混標(biāo)/BJS 201701廠家;TMstandard

公司簡(jiǎn)介

成立日期 2018-06-11 (7年) 注冊(cè)資本 5000萬(wàn)人民幣
員工人數(shù) 100-500人 年?duì)I業(yè)額 ¥ 500萬(wàn)-1000萬(wàn)
主營(yíng)行業(yè) 經(jīng)營(yíng)模式
  • 壇墨質(zhì)檢科技股份有限公司
非會(huì)員
  • 公司成立:7年
  • 注冊(cè)資本:5000萬(wàn)人民幣
  • 企業(yè)類型:方燕飛
  • 主營(yíng)產(chǎn)品:臺(tái)盼藍(lán)染色原理模擬活/死細(xì)胞濃度和比例標(biāo)準(zhǔn)物質(zhì)/4℃下可以長(zhǎng)期穩(wěn)定保存,銅綠假單胞菌/定性/0代/標(biāo)準(zhǔn)菌株/有證書(shū)/GB 4789.28/有效期至2028-12-31/含冰袋運(yùn)輸費(fèi),土壤成分分析標(biāo)準(zhǔn)物質(zhì)-安徽潮土
  • 公司地址:
詢盤

標(biāo)準(zhǔn)品/甲醇中4種藥物混標(biāo)/BJS 201701相關(guān)廠家報(bào)價(jià)

產(chǎn)品名稱 價(jià)格   公司名稱 報(bào)價(jià)日期
詢價(jià)
VIP1年
北京海岸鴻蒙標(biāo)準(zhǔn)物質(zhì)技術(shù)有限責(zé)任公司
2024-12-18
詢價(jià)
VIP3年
北京譜析科技有限公司
2024-12-23
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