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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → L-Cysteine hydrochloride monohydrate

HRID 416677
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HRID 416677 반응식
[ClH:1].[NH2:2][C@H:3]([C:6]([OH:8])=[O:7])[CH2:4][SH:5]>>[OH2:7].[ClH:1].[NH2:2][C@H:3]([C:6]([OH:8])=[O:7])[CH2:4][SH:5]
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참가 물질

3

반응물 2

HCID 313Hydrochloric AcidHCID 5862L-(+)-Cysteine2회

생성물 1

HCID 23462L-Cysteine hydrochloride monohydrate

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온도
-10 °C

실험 절차

500 ml of a purified L-cysteine-containing solution (eluate with 1N HCl) of example 7 or 9 (L-cysteine content=17 g/l) are concentrated to 25 ml. After adding concentrated HCl or introducing HCl gas, chlorides of inorganic alkali metal and alkaline earth metal ions and ammonium chloride may be crystallized, preferably at 20-60° C. After filtration, the L-cysteine-containing mother liquor is cooled to −10° C. and L-cysteine hydrochloride monohydrate crystallizes. Depending on the purity of the L-cysteine-containing solution used, L-cysteine hydrochloride monohydrate may be obtained in crystalline form in yields of >80% and purities of >90% from these solutions. It is possible to achieve purities of up to >98% by suitable control of the crystallization conditions, fractionated crystallization and/or recrystallization.

후처리

  1. concentrationare concentrated to 25 ml
  2. additionAfter adding concentrated HCl
  3. additionintroducing HCl gas, chlorides of inorganic alkali metal and alkaline earth metal ions and ammonium chloride
  4. custommay be crystallized, preferably at 20-60° C
  5. filtrationAfter filtration
  6. additionthe L-cysteine-containing mother liquor
  7. customL-cysteine hydrochloride monohydrate crystallizes
  8. additioncontaining solution

출처 및 근거

ORD 기록
ord-25b21d06295f4ec6a1f72a2e675fa149
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08088949B2

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