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15775-74-3

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15775-74-3 Usage

Uses

Different sources of media describe the Uses of 15775-74-3 differently. You can refer to the following data:
1. Progesterone-d9 is intended for use as an internal standard for the quantification of Progesterone by GC- or LC-mass spectrometry.
2. Steroid hormone produced by the corpus luteum. Induces maturation and secretory activity of the uterine endothelium; suppresses ovulation. Progesterone is implicated in the etiology of breast cancer.

General Description

Progesterone, a steroid hormone of the progestogen class, is used for hormone replacement therapy. This internal standard is applicable for progesterone testing or isotope dilution methods by GC/MS or LC/MS for endocrinology, female health testing or clinical chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 15775-74-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,7,7 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15775-74:
(7*1)+(6*5)+(5*7)+(4*7)+(3*5)+(2*7)+(1*4)=133
133 % 10 = 3
So 15775-74-3 is a valid CAS Registry Number.

15775-74-3 Well-known Company Product Price

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  • Cerilliant

  • (P-070)  Progesterone-D9 solution  100 μg/mL in acetonitrile, ampule of 1 mL, certified reference material

  • 15775-74-3

  • P-070-1ML

  • 3,656.25CNY

  • Detail

15775-74-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name PROGESTERONE-2,2,4,6,6,17ALPHA,21,21,21-D9

1.2 Other means of identification

Product number -
Other names progesterone-2,2,4,6,6,17,21,21,21-d9

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:15775-74-3 SDS

15775-74-3Upstream product

15775-74-3Downstream Products

15775-74-3Relevant articles and documents

Bhacca,N.S.,Giannini,D.D.

, p. 8421 (1973)

ACTIVATION OF WATER MOLECULES - 2. GENERATION OF STRONG HYDROXO BASES BY THE REACTION OF WATER WITH PLATINUM (0) PHOSPHINE COMPLEXES AND THE APPLICATIONS AS CATALYSTS FOR H-D EXCHANGE AND HYDRATION REACTIONS.

Yoshida,Matsuda,Okano,Kitani,Otsuka

, p. 2027 - 2038 (2007/10/05)

The dissociation of Pt(PEt//3)//4 in organic solvents (THF, n-heptane) occurs to give Pt(PEt//3)//3 L equals 0. 5 M in THF at 20 degree C), no further dissociation being detected, while Pt left bracket P(i-Pr)//3 right bracket //3, upon dissolution in the above solvents, exists mainly as Pt left bracket P(i-Pr)//3 right bracket //2 (K//L equals 0. 14 M in THF at 20 degree chemical Addition of water to PtL//(L equals PEt//3//, P(i-Pr)//3) generates strong hydroxy bases, left bracket PtHL//3 right bracket OH (L equals PEt//3) or trans- left bracket PtH(S)L//2 right bracket OH (L equals P(i-Pr)//3//, S equals solvent), while the addition to Pt left bracket P(i-Pr)//3 right bracket //2 gives a sigma -hydrido hydroxo compound, trans-PtH(OH) left bracket P(i-Pr)//3 right bracket //2. Quantitative study on the reversible water addition to PtL//3 in organic solvents was carried out by pH and conductance measurements. The conductometric behaviors of the system PtL//3(L equals PEt//3)/H//2O in pyridine and THF are described in terms of two equilibria. The mechanism was studied for H-D exchange of C//6H//5COCH//3 to show that the reaction follows a rate equation, R equals k left bracket Pt right bracket left bracket C//6H//5COCH//3 right bracket , and involves a reversible condensation, M** plus OD** minus plus C//6H//5COCH//3 reversible reaction MCH// 2COC//6H//5 plus DHO, as the rate-determining step. Unlike the alkaline base-catalyzed reaction, alpha -olefinic, allylic, and aldehydic hydrogen atoms of alpha , beta -unsaturated carbonyl compounds were exchanged. The hydration of the nitrile and double bonds of RCH equals CHCN catalyzed by left bracket PtHL//3 right bracket OH or left bracket PtH(S)L//2 right bracket OH and trans-Pt(OH)(R)(PPh//3)//2 occurs with excellent chemical yields.

Mass spectrometry of steroid systems. X. Determination of the configuration at C-17 in the pregnene-3,20-dione series.

Zaretskii,Wulfson,Zaikin

, p. 3683 - 3686 (2007/10/06)

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