하이드록시프롤린

하이드록시프롤린
하이드록시프롤린 구조식 이미지
카스 번호:
51-35-4
한글명:
하이드록시프롤린
동의어(한글):
하이드록시프롤린;4-하이드록시프롤린
상품명:
L-Hydroxyproline
동의어(영문):
TRANS-4-HYDROXY-L-PROLINE;HYDROXYPROLINE;(2S,4R)-4-HYDROXYPYRROLIDINE-2-CARBOXYLIC ACID;Hyp;4-Hydroxyproline;4-HYDROXY-L-PROLINE;H-HYP-OH;4-HYDROXYPYRROLIDINE-2-CARBOXYLIC ACID;HYDROXY-L-PROLINE;4R-4-hydroxyproline
CBNumber:
CB8357870
분자식:
C5H9NO3
포뮬러 무게:
131.13
MOL 파일:
51-35-4.mol
MSDS 파일:
SDS

하이드록시프롤린 속성

녹는점
273 °C (dec.)(lit.)
알파
-75.5 º (c=5, H2O)
끓는 점
242.42°C (rough estimate)
밀도
1.3121 (rough estimate)
증기 밀도
4.5 (vs air)
굴절률
-75.5 ° (C=4, H2O)
저장 조건
Store below +30°C.
용해도
H2O: 50 mg/mL
물리적 상태
결정 또는 결정성 분말
산도 계수 (pKa)
1.82, 9.66(at 25℃)
색상
하얀색
수소이온지수(pH)
5.5-6.5 (50g/l, H2O, 20℃)
냄새
냄새 없는
optical activity
[α]25/D 75.6°, c = 1 in H2O
수용성
357.8g/L(20℃)
Merck
14,4840
BRN
471933
InChIKey
PMMYEEVYMWASQN-DMTCNVIQSA-N
LogP
-0.350 (est)
CAS 데이터베이스
51-35-4(CAS DataBase Reference)
NIST
Hydroxyproline(51-35-4)
EPA
trans-4-Hydroxy-L-proline (51-35-4)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xi,Xn
위험 카페고리 넘버 36/37/38-22
안전지침서 24/25-36/37/39-27-26
WGK 독일 3
RTECS 번호 TW3586500
TSCA Yes
위험 등급 IRRITANT
HS 번호 29339990
그림문자(GHS): GHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H315 피부에 자극을 일으킴 피부부식성 또는 자극성물질 구분 2 경고 GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 눈에 심한 자극을 일으킴 심한 눈 손상 또는 자극성 물질 구분 2A 경고 GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H335 호흡 자극성을 일으킬 수 있음 특정 표적장기 독성 - 1회 노출;호흡기계 자극 구분 3 경고 GHS hazard pictograms
예방조치문구:
P261 분진·흄·가스·미스트·증기·...·스프레이의 흡입을 피하시오.
P271 옥외 또는 환기가 잘 되는 곳에서만 취급하시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
NFPA 704
1
0 0

하이드록시프롤린 MSDS


(2S,4R)-(-)-4-Hydroxy-2-pyrrolinecarboxylic acid

하이드록시프롤린 C화학적 특성, 용도, 생산

개요

A non-essential amino acid. Can be isolated from gelatin. Hydroxyproline has not been reported as added to food in any of the NAS surveys.

화학적 성질

White crystalline powder

용도

A natural constituent of animal structural proteins such as collagen and elastin. Several microorganisms producing proline trans-4- and cis-3-hydroxylase were discovered and these enzymes were applied to the industrial production of trans-4- and cis-3-hydroxy-L-proline.

정의

ChEBI: An optically active form of 4-hydroxyproline having L-trans-configuration.

생산 방법

In the past L-Hydroxyproline was isolated by hydrolysis of animal collagen, e. g. gelatine or collagen, of which it is a major constituent. L-Hydroxyproline is an unnatural amino acid which is made in the body by hydroxylation of L-Proline. The presence of L-Hydroxyproline and proline are key to maintaining the stability of the tight collagen helix.
Today L-Hydroxyproline is manufactured by bio-catalysed hydroxylation of proline in bacteria. Together with its other isomers, L-Hydroxyproline is also used as an inter mediate for a range of pharmaceutical active ingredients.
Produced by hydroxylation of L-proline after protein synthesis. It is contained rich in collagen and elastin. Known to stabilization of triple-helix structure of collagen. Widely used as an intermediate for medicines.

일반 설명

Pharmaceutical secondary standards for application in quality control provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards

Purification Methods

Crystallise it from MeOH/EtOH (1:1). Separation from normal allo-isomer can be achieved by crystallisation of the copper salts [see Levine Biochemical Preparations 8 114 1961]. Separation from proline is achieved via the crystalline picrate, CdCl2, or acid ammonium rhodanate salts [see Greenstein & Winitz The Chemistry of the Amino Acids J. Wiley, Vol 3 p 2182 1961, Kapfhammer & Mohn Z Physiol Chem 306 76 1956]. [Beilstein 22/5 V 7.]

하이드록시프롤린 준비 용품 및 원자재

원자재

준비 용품


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