93370
1,1,1-Tris(hydroxymethyl)propane
dist., ≥98.0% (GC)
동의어(들):
2-Ethyl-2-hydroxymethyl-1,3-propanediol, Trimethylolpropane
로그인조직 및 계약 가격 보기
모든 사진(1)
About This Item
Linear Formula:
CH3CH2C(CH2OH)3
CAS Number:
Molecular Weight:
134.17
Beilstein:
1698309
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
vapor density
4.8 (vs air)
Quality Level
vapor pressure
<1 mmHg ( 20 °C)
분석
≥98.0% (GC)
양식
(Powder or Crystals or Granules or Chunks)
autoignition temp.
1301 °F
품질
dist.
bp
159-161 °C/2 mmHg (lit.)
mp
56-58 °C (lit.)
56-61 °C
solubility
H2O: 0.1 g/mL, clear
작용기
hydroxyl
SMILES string
CCC(CO)(CO)CO
InChI
1S/C6H14O3/c1-2-6(3-7,4-8)5-9/h7-9H,2-5H2,1H3
InChI key
ZJCCRDAZUWHFQH-UHFFFAOYSA-N
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애플리케이션
1,1,1-Tris(hydroxymethyl)propane is used as a starting material in the synthesis of a variety of polyglycerols and polylactides. It is also used as a tripodal ligand to construct manganese-based metal-organic complexes as single molecular magnets.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Repr. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point (°F)
356.0 °F - Cleveland open cup
Flash Point (°C)
180 °C - Cleveland open cup
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
이미 열람한 고객
Telechelic and star-shaped poly (L-lactide) s by means of bismuth (III) acetate as initiator.
Kricheldorf HR, et al.
Biomacromolecules, 5(2), 492-496 (2004)
A family of manganese rods: Syntheses, structures, and magnetic properties.
Rajaraman G, et al.
Journal of the American Chemical Society, 126(47), 15445-15457 (2004)
Synthesis, characterization, and viscoelastic properties of high molecular weight hyperbranched polyglycerols.
Kainthan RK, et al.
Macromolecules, 39(22), 7708-7717 (2006)
Synthesis, structure, and magnetic properties of a [Mn22] wheel-like single-molecule magnet.
Murugesu M, et al.
Inorganic Chemistry, 43(14), 4203-4209 (2004)
Zhongyu Li et al.
Bioconjugate chemistry, 22(3), 518-522 (2011-02-11)
A synthetic route to prepare acetal-protected heterobifunctional poly(ethylene glycol), allyl(1-ethoxyethoxy)-PEG-OH (allyl(EE)-PEG-OH), was successfully established using a newly synthesized initiator, trimethylolpropane allyl (1-ethoxyethoxy) ether (TMPAEEE). Heterobifunctional allyl(OH)-mPEG and heterotrifunctional allyl(OH)-PEG-alkyne were obtained, respectively, after modification from this precursor polymer. The polymers
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