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H-085

17α-羟孕酮标准液溶液

Name: 17α-羟孕酮标准液 溶液
Brand: CERILLIAN

1.0 mg/mL in methanol, ampule of 1 mL, certified reference material, Cerilliant^®

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经验公式（希尔记法）:

C₂₁H₃₀O₃

CAS号:

68-96-2

分子量:

330.46

MDL编号:

MFCD00003659

PubChem化学物质编号:

329815138

NACRES:

NA.24

等级

certified reference material

质量水平

300

形式

liquid

特点

Snap-N-Spike^®/Snap-N-Shoot^®

包装

ampule of 1 mL

manufacturer/tradename

Cerilliant^®

浓度

1.0 mg/mL in methanol

technique(s)

gas chromatography (GC): suitable
liquid chromatography (LC): suitable

application(s)

clinical testing
clinical testing

格式

single component solution

储存温度

−20°C

SMILES string

CC(=O)[C@@]1(O)CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C

InChI

1S/C21H30O3/c1-13(22)21(24)11-8-18-16-5-4-14-12-15(23)6-9-19(14,2)17(16)7-10-20(18,21)3/h12,16-18,24H,4-11H2,1-3H3/t16-,17+,18+,19+,20+,21+/m1/s1

InChI key

DBPWSSGDRRHUNT-CEGNMAFCSA-N

一般描述

用于LC-MS/MS新生儿筛查试验的校准物料。这种经认证的加标溶液^®适用于临床和研究环境中的许多关键应用，从质控品和系统调整/适用性标准品的制备到试剂制备和试剂和含量测定开发中的OEM使用。

法律信息

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany

CERTIFIED SPIKING SOLUTION is a registered trademark of Cerilliant Corporation

Snap-N-Shoot is a registered trademark of Cerilliant Corporation

Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany

警示用语：

Danger

危险声明

H225 - H301 + H311 + H331 - H370

预防措施声明

P210 - P233 - P280 - P301 + P310 - P303 + P361 + P353 - P304 + P340 + P311

危险分类

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

储存分类代码

3 - Flammable liquids

WGK

WGK 2

闪点(°F)

49.5 °F - closed cup

闪点(°C)

9.7 °C - closed cup

法规信息

危险化学品

分析证书(COA)

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示例

T1503

货号

25G

包装规格/数量

其它示例：

705578-5MG-PW

PL860-CGA/SHF-1EA

MMYOMAG-74K-13

1000309185

输入内容 1.000309185)

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Reverse-hybridization assay for rapid detection of common CYP21A2 mutations in dried blood spots from newborns with elevated 17-OH progesterone.

Stefan Németh et al.

Clinica chimica acta; international journal of clinical chemistry, 414, 211-214 (2012-09-19)

Congenital adrenal hyperplasia (CAH) is an autosomal recessive disorder most commonly caused by defects in the CYP21A2 gene. Neonatal CAH-screening based on 17-hydroxyprogesterone (17-OHP) measurements prevents life-threatening salt wasting conditions in newborns, but results in a considerable false-positive rate. Therefore

Serum 17-OH progesterone and free testosterone levels in women patients with Familial Mediterranean Fever: a pivotal study.

K Deveci et al.

European review for medical and pharmacological sciences, 17(2), 261-265 (2013-02-05)

Familial Mediterranean Fever (FMF) is an autosomal recessive disease characterized by short lived, febrile serosae inflammatory attacks. FMF has various effects in multiple systems and organs. In the present study, our aim was to evaluate adrenal steroidogenesis in female FMF

Plasma adiponectin levels in women with polycystic ovary syndrome: impact of metformin treatment in a case-control study.

Shilpi Singh et al.

Diabetes & metabolic syndrome, 6(4), 207-211 (2012-12-04)

An interaction between adiponectin, steroid synthesis or action and measures of insulin resistance (IR) have been reported in the pathogenesis of polycystic ovary syndrome (PCOS). The present study was done to determine plasma adiponectin concentration (PAC) in women with and

Effects of metformin on serum insulin and anti-Mullerian hormone levels and on hyperandrogenism in patients with polycystic ovary syndrome.

Areana Diogo Nascimento et al.

Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology, 29(3), 246-249 (2012-12-01)

To evaluate the relationship between serum anti-Mullerian hormone levels (AMH) and insulin resistance (IR) before and after meformin treatment and to compare AMH levels of polycystic ovary syndrome (PCOS) women in the early follicular phase. Twenty PCOS women with IR

Erroneous prenatal diagnosis of congenital adrenal hyperplasia owing to a duplication of the CYP21A2 gene.

O Lekarev et al.

Journal of perinatology : official journal of the California Perinatal Association, 33(1), 76-78 (2012-12-28)

Congenital adrenal hyperplasia (CAH) is an autosomal recessive disorder where steroidogenesis in the adrenal cortex is impaired. The most common form is caused by 21-hydroxylase deficiency (21OHD). Classical 21OHD is characterized by glucocorticoid and mineralocorticoid deficiency and by overproduction of

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17α-羟孕酮标准液 溶液

1.0 mg/mL in methanol, ampule of 1 mL, certified reference material, Cerilliant®

属性

等级

质量水平

形式

特点

包装

manufacturer/tradename

浓度

technique(s)

application(s)

格式

储存温度

SMILES string

InChI

InChI key

相关类别

说明

一般描述

法律信息

相关产品

相关产品

安全信息

象形图

警示用语：

危险声明

预防措施声明

危险分类

储存分类代码

WGK

闪点(°F)

闪点(°C)

法规信息

文件

分析证书(COA)

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17α-羟孕酮标准液溶液

1.0 mg/mL in methanol, ampule of 1 mL, certified reference material, Cerilliant^®