2'-Deoxycytidine

2'-Deoxycytidine 구조식 이미지
카스 번호:
951-77-9
상품명:
2'-Deoxycytidine
동의어(영문):
DC;deoxycytidine;4-AMino-1-((2R,4S,5R)-4-hydroxy-5-(hydroxyMethyl)tetrahydrofuran-2-yl)pyriMidin-2(1H)-one;dCyd;2-Deoxycystidine;Cytosine deoxyribonucleoside;4-amino-1-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-pyrimidin-2-one;2'-DC;2'Isomer Only)
CBNumber:
CB7452978
분자식:
C9H13N3O4
포뮬러 무게:
227.22
MOL 파일:
951-77-9.mol
MSDS 파일:
SDS

2'-Deoxycytidine 속성

녹는점
209-211 °C(lit.)
끓는 점
368.93°C (rough estimate)
밀도
1.3171 (rough estimate)
굴절률
59 ° (C=1, H2O)
저장 조건
-20°C
용해도
H2O: 50 mg/mL, 투명, 무색
물리적 상태
결정성 분말
산도 계수 (pKa)
14.03±0.60(Predicted)
색상
하얀색
수용성
물에 불용성, DMSO.
BRN
87567
InChI
InChI=1S/C9H13N3O4/c10-7-1-2-12(9(15)11-7)8-3-5(14)6(4-13)16-8/h1-2,5-6,8,13-14H,3-4H2,(H2,10,11,15)/t5-,6+,8+/m0/s1
InChIKey
CKTSBUTUHBMZGZ-SHYZEUOFSA-N
SMILES
OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)C[C@@H]1O
CAS 데이터베이스
951-77-9(CAS DataBase Reference)
NIST
Deoxycytidine(951-77-9)
EPA
Cytidine, 2'-deoxy- (951-77-9)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
안전지침서 24/25
WGK 독일 3
RTECS 번호 HA3800000
F 고인화성물질 10
TSCA Yes
HS 번호 29349990
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:
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P302+P352 피부에 묻으면 다량의 물로 씻으시오.
P304+P340 흡입하면 신선한 공기가 있는 곳으로 옮기고 호흡하기 쉬운 자세로 안정을 취하시오.
NFPA 704
0
1 0

2'-Deoxycytidine MSDS


2'-Deoxycytidine monohydrate

2'-Deoxycytidine C화학적 특성, 용도, 생산

화학적 성질

White crystalline powder

용도

A deoxyribonucleoside

정의

ChEBI: A pyrimidine 2'-deoxyribonucleoside having cytosine as the nucleobase.

일반 설명

2′-Deoxycytidine (deoxyC) is one of the deoxynucleosides containing cytosine as the nucleobase. It is found in the blood, feces, and urine.

Safety Profile

Experimental reproductive effects. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx.

Purification Methods

Purify 2'-deoxycytidine by recrystallisation from MeOH/Et2O or EtOH and dry it in air. [NMR: Miles J Am Chem Soc 85 1007 1963, UV: Fox & Shugar Biochim Biophys Acta 9 369 1952.] The hydrochloride crystallises from H2O/EtOH and has m 174o(dec, 169-173o). [Walker & Butler Can J Chem 34 1168 1956.] The picrate has m 208o(dec). [Fox et al. J Am Chem Soc 83 4066 1961, Beilstein 25 III/IV 3662.]

Structure and conformation

2'-Deoxycytidine monohydrate (dCMP) is a nucleoside phosphate in being comprised of a deoxyribonucleoside and one phosphate group. It has a deoxyribose as its sugar constituent with one phosphate group attached. Its nucleoside contains a pyrimidine base, i.e., a cytosine attached to the deoxyribose sugar. It has only one phosphate group attached to the nucleoside. Its conjugate acid form is deoxycytidylic acid, whereas its conjugate base form is deoxycytidylate. dCMP, instead of having a hydroxyl group on the 2′ carbon of the sugar component as it is in Cytidine monophosphate (CMP), has it reduced to a hydrogen atom (thus, deoxy- in its name). dCMP is one of the monomeric units that constitute DNA, whereas CMP is one of the monomeric units that make up RNA.

2'-Deoxycytidine 준비 용품 및 원자재

원자재

준비 용품


2'-Deoxycytidine 공급 업체

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