추천 제품
Quality Level
분석
97%
형태
liquid
refractive index
n20/D 1.483 (lit.)
bp
174.3 °C (lit.)
mp
−4 °C (lit.)
solubility
water: soluble 10 part
alcohol: miscible
diethyl ether: miscible
density
1.363 g/mL at 20 °C
1.351 g/mL at 25 °C (lit.)
SMILES string
OC(CCl)CCl
InChI
1S/C3H6Cl2O/c4-1-3(6)2-5/h3,6H,1-2H2
InChI key
DEWLEGDTCGBNGU-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
1,3-Dichloro-2-propanol is a food processing contaminant. Biotransformation of 1,3-dichloro-2-propanol to epichlorohydrin by the whole cells of recombinant Escherichia coli via resin-based in situ product removal has been investigated.
1,3-Dichloro-2-propanol is used as a pharmaceutical intermediate and solvent for paints, lacquers, and epoxy resins.
1,3-Dichloro-2-propanol is used as a pharmaceutical intermediate and solvent for paints, lacquers, and epoxy resins.
애플리케이션
1,3-Dichloro-2-propanol can be used as a reactant to synthesize:
It can also be used as an intermediate in the production of epoxy resins, as well as a solvent for hard resins and nitrocellulose.
- Hydroxyl-N-tosylcyclams via sodium ethoxide catalyzed cyclization reaction with di(poly)-N-tosylamides.
- (R)-Epichlorohydrin using biocatalysts.
- 1,3-dichloropropene, a soil fumigant, and synthetic glycerol.
It can also be used as an intermediate in the production of epoxy resins, as well as a solvent for hard resins and nitrocellulose.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Carc. 1B
Storage Class Code
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
Flash Point (°F)
186.8 °F - closed cup
Flash Point (°C)
86 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
Biotechnology letters, 35(6), 937-942 (2013-02-23)
Biotransformation of 1,3-dichloro-2-propanol (DCP) to epichlorohydrin (ECH) by the whole cells of recombinant Escherichia coli expressing halohydrin dehalogenase was limited by product inhibition. To solve this problem and improve the ECH yield, a biotransformation strategy using resin-based in situ product
Soy-based adhesives with 1, 3-dichloro-2-propanol as a curing agent
Wood and Fiber Science, 36(2), 186-194 (2004)
Direct preparation kinetics of 1, 3-dichloro-2-propanol from glycerol using acetic acid catalyst
Industrial & Engineering Chemistry Research, 48, 446-452 (2009)
Role of mitogen-activated protein kinases and nuclear factor-kappa B in 1, 3-dichloro-2-propanol-induced hepatic injury
Laboratory Animal Research, 32(1), 24-33 (2016)
Production of (R)-epichlorohydrin from 1, 3-dichloro-2-propanol by two-step biocatalysis using haloalcohol dehalogenase and epoxide hydrolase in two-phase system
Biochemical Engineering Journal, 74, 1-7 (2013)
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