D(-)-Tartaric acid

D(-)-Tartaric acid 구조식 이미지
카스 번호:
526-83-0
상품명:
D(-)-Tartaric acid
동의어(영문):
(2R,3S)-2,3-Dihydroxybernsteinsaeure;(2R,3R)-2,3-Dihydroxybernsteinsaeure;L-tartaricaci;D-2,3-Dihydroxysuccinic acid;Acacia senegal、Acacia seyal;D(-)-Tartaric acid;Tartaric Acid Impurity 6;D(-)-Tartaric acid, 98%+;Dihydroxybernsteinsaeure;high quality D(-)-Tartaric acid
CBNumber:
CB6663151
분자식:
C4H6O6
포뮬러 무게:
150.09
MOL 파일:
526-83-0.mol

D(-)-Tartaric acid 속성

녹는점
159-171°C
끓는 점
399.3±42.0 °C(Predicted)
밀도
1.886±0.06 g/cm3(Predicted)
저장 조건
Sealed in dry,Room Temperature
용해도
DMSO(약간, 가열), 메탄올(약간), 물(적게, 초음파 처리)에 용해됨
물리적 상태
고체
물리적 상태
단단한 모양
산도 계수 (pKa)
3.07±0.34(Predicted)
색상
흰색에서 황백색까지
냄새
100.00%에서. 냄새 없는
?? ??
냄새 없는
InChI
InChI=1S/C4H6O6/c5-1(3(7)8)2(6)4(9)10/h1-2,5-6H,(H,7,8)(H,9,10)
InChIKey
FEWJPZIEWOKRBE-UHFFFAOYSA-N
SMILES
C(O)(=O)C(O)C(O)C(O)=O
LogP
-1.081 (est)
EPA
2,3-Dihydroxysuccinic acid (526-83-0)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
HS 번호 29181200
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
예방조치문구:
P305+P351+P338 눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.

D(-)-Tartaric acid C화학적 특성, 용도, 생산

개요

Tartaric acid is a white crystalline diprotic aldaric acid. It occurs naturally in many plants, particularly grapes, bananas, and tamarinds, is commonly combined with baking soda to function as a leavening agent in recipes, and is one of the main acids found in wine. It is added to other foods to give a sour taste, and is used as an antioxidant. Salts of tartaric acid are known as tartrates. It is a dihydroxyl derivative of succinic acid.
Tartaric acid was first isolated from potassium tartrate, known to the ancients as tartar, circa 800 AD, by the alchemist Jabir ibn Hayyan The modern process was developed in 1769 by the Swedish chemist Carl Wilhelm Scheele.
Tartaric acid played an important role in the discovery of chemical chirality. This property of tartaric acid was first observed in 1832 by Jean Baptiste Biot, who observed its ability to rotate polarized light. Louis Pasteur continued this research in 1847 by investigating the shapes of ammonium sodium tartrate crystals, which he found to be chiral. By manually sorting the differently shaped crystals under magnification, Pasteur was the first to produce a pure sample of levotartaric acid.

용도

Pharmaceutic aid (buffering agent).

정의

A crystalline naturallyoccurring carboxylic acid,(CHOH)2(COOH)2; r.d. 1.8; m.p.171–174°C. It can be obtained fromtartar (potassium hydrogen tartrate)deposits from wine vats, and is usedin baking powders and as a foodstuffsadditive. The compound isoptically active (see optical activity).The systematic name is 2,3-dihydroxybutanedioic acid.

D(-)-Tartaric acid 준비 용품 및 원자재

원자재

준비 용품


D(-)-Tartaric acid 공급 업체

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