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EP 레 보노 게스트 렐 불순물 D메이커 CAS 레지스트리 번호32419-58-2공급업체 | LookChem

EP 레 보노 게스트 렐 불순물 D

기본 정보 Edit
  • 표준명:EP 레 보노 게스트 렐 불순물 D
  • CAS 레지스트리 번호:32419-58-2
  • 분자식:C21H30O
  • 분자 무게:298.469
  • HS 코드:
  • Mol 파일:32419-58-2.mol
EP 레 보노 게스트 렐 불순물 D

동의어: 13-Ethyl-18,19-dinor-17α-pregn-4-en-20-yn-17-ol
(Levo Norgestrel Impurity);(17α)-13-Ethyl-18,19-dinorpregn-4-en-20-yn-17-ol;13-Ethyl-18,19-dinor-17a-pregn-4-en-20-yn-17-ol
(Levo Norgestrel IMpurity); Levonorgestrel IMpurity D; 13-Ethyl-18,19-dinor-17α-pregn-4-en-20-yn-17-ol (Levonorgestrel Impurity D); (17a) -13-Ethyl-18,19 , 4-dinorpregn-20-en-17-yn-13-ol; 18,19-Ethyl-17-dinor-4a-pregn-20-en-17-yn-XNUMX-ol (Levonorgestrel Impurity D); EP Levonorgestrel 불순물 D

관련 CAS 번호: 383127-22-8 34662-32-3 34874-54-9 38707-83-4 351410-38-3 321660-77-9 371157-17-4 329709-90-2 33647-67-5 362669-52-1

표준명의 마케팅 및 가격
제조업체 및 유통업체:
  • 제조/브랜드
  • 화학물질 및 원자재
  • 포장
  • 가격
  • Biosynth Carbosynth
  • 13-Ethyl-18,19-dinor-17a-pregn-4-en-20-yn-17-ol - EP
  • 25 mg
  • $ 1529.00
  • Biosynth Carbosynth
  • 13-Ethyl-18,19-dinor-17a-pregn-4-en-20-yn-17-ol - EP
  • 10 mg
  • $ 840.90
  • Biosynth Carbosynth
  • 13-Ethyl-18,19-dinor-17a-pregn-4-en-20-yn-17-ol - EP
  • 5 mg
  • $ 462.50
  • Biosynth Carbosynth
  • 13-Ethyl-18,19-dinor-17a-pregn-4-en-20-yn-17-ol - EP
  • 2 mg
  • $ 254.40
  • Biosynth Carbosynth
  • 13-Ethyl-18,19-dinor-17a-pregn-4-en-20-yn-17-ol - EP
  • 1 mg
  • $ 139.90
총 7 개 원재료 공급업체
표준명의 화학적 성질 Edit
물리적 데이터:
안전정보:
  • 픽토그램:
  • 위험 코드:
  • 진술:
  • 안전 선언문:
사용:
  • 소개 및 적용: Levonorgestrel EP Impurity D (13-Ethyl-18,19-dinor-17α-pregn-4-en-20-yn-17-ol) is an impurity found in Levonorgestrel, which is a synthetic progestin hormone used in various contraceptive and hormonal treatments. In pharmaceutical applications, it is important to monitor and control the levels of impurities like Levonorgestrel EP Impurity D to ensure the safety, efficacy, and quality of the final product. The use of EP Levonorgestrel impurity D is primarily in the context of pharmaceutical manufacturing and quality control processes, where it is utilized as a reference substance for the identification and quantification of this specific impurity in Levonorgestrel products. By using this impurity as a reference, manufacturers can ensure that their products meet the required standards and regulations for quality and purity, ultimately contributing to the overall safety and effectiveness of the medication.
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