Elagolix Sodium High Quality Raw Material NBI 56418NA Powder CAS 832720-36-2

  • CasNo832720-36-2
  • Molecular Formula C32H29F5N3NaO5
  • Purity99.5%
  • AppearanceWhite Powder
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Product Details

Quick Details

  • CasNo: 832720-36-2
  • Molecular Formula: C32H29F5N3NaO5
  • Appearance: White Powder
  • Delivery Time: 3days after we receive the payment
  • Throughput: 1000|Kilogram|Month
  • Purity: 99.5%

High quality raw material NBI 56418NA powder CAS 832720-36-2

Item Name: Elagolix Sodium

CAS NO.: 832720-36-2

Apparence: White Powder

package: Aluminum Bag;Drums

Purity: 99%

Storage: Store in a tightly closed container and cool dry place where the temperature stays below 20℃

Certificate: ISO9001

Payment: T/T;Western Union

What is Elagolix Sodium

As an organic synthesis intermediate and pharmaceutical intermediate, Elagolix Sodium is mainly used in laboratory research and development process and chemical and pharmaceutical synthesis process.

 

Elagolix has been used in trials studying the basic science and treatment of Endometriosis, Folliculogenesis, Uterine Fibroids, Heavy Uterine Bleeding, and Heavy Menstrual Bleeding. As of 24 July 2018, however, the U.S. Food and Drug Administration (FDA) approved AbbVie's elagolix under the brand name Orilissa as the first and only oral gonadotropin-releasing hormone (GnRH) antagonist specifically developed for women with moderate to severe endometriosis pain.

 

Certificate of Analysis

TEST

SPECIFICATIONS

RESULTS

Characters

A white or almost white
Crystalline powder,
Hygroscopic. Freely soluble
in water, very soluble in methanol, freely soluble in methylene chloride.

Conform

Identification

A) IR graph should be concordant
with reference spectrum of Xylazine Hydrochloride.
B) the paper turns violet-red.

Conform

Appearance of solution

Solution S should not be more
opalescent than reference
Suspension II and should be colourless.

Conform

pH

4.5 to 5.5

5.1

Impurity A

Not more than 100 ppm.

Conform

Related substances

A) Impurities C and E (for each impurity): Not more than 0.2%.
B) Impurities B and D (for each impurity): Not more than 0.2%.
C) Any other impurity: Not more than 0.2%.
D) Total impurities other
Than B,C,D and E : Not more than 0.2%.

Conform

Loss on drying

Not more than 0.5%

0.32%

Heavy metals

Not more than 10ppm

Complies

Sulphated ash

Not more than 0.100%

0.02%

Assay

98.0% ~ 102.0%
Calculated on dried basis

99.97%

Residual solvents
Acetone
Xylene


Not more than 300ppm
Not more than 300ppm
Not more than 300ppm
Not more than 300ppm


Conforms
Conforms
Conforms
Conforms

BIOLOGICAL TESTS

NOT MORE THAN 104 EU/g

Conform

 

1.used in the treatment of moderate to severe pain associated with endometriosis in premenopausal women;
2.approved only for the treatment of endometriosis; 
3.Other approved for uterine fibroids and breast cancer in premenopausal women, prostate cancer in men, precocious puberty in children, and hormone therapy in transgender adolescents and adults, among others.

 

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