(±)-trans- 1,2-Diaminocyclohexane CAS 1121-22-8 Puritas ≥98.0% Alta Puritas

Description:

Nomen chemicum: (±)-trans 1,2-Diaminocyclohexane

CAS: 1121-22-8

Aspectus: hyalina vel flavescens Liquid

Puritas: ≥98.0%

High Quality, Commercial Production

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Product Detail

Product Tags

Descriptio:

Manufacturer Supple cum High puritate et stabulo Quality
Nomen chemicum: (±)-trans 1,2-Diaminocyclohexane
CAS: 1121-22-8
High Quality, Commercial Production

Chemical Properties:

Nomen chemicum	(±)-trans 1,2-Diaminocyclohexane
Synonyma	trans-1,2-Diaminocyclohexane;trans-1,2-Cyclohexanediamine
CAS Number	1121-22-8
CATTUS Number	RF-CC281
Stock Status	In Stock, Productio Ascendite ad Tons
Formulae hypotheticae	C6H14N2
M. Pondus	114.19
Liquescens punctum	14.0-15.0℃ (lit.)
Ferveret	79.0-81.0℃/15 mmHg (lit.)
Density	0.951 g/mL ad 25℃ (lit.)
Index refractivus	n20/D 1.489 (lit.)
Solubilitas	Solutum in aqua
Sensibilitas	Aer Sensitivus, Hygroscopic
Shipping Condition	Uit sub Ambient Temperature
Brand	Ruifu Chemical

Specifications:

Item	Specifications
Aspectus	Hyalina vel flavescens Liquid
Puritas	≥98.0% (GC)
Aqua	≤1.00%
Totalis immunditias	≤2.00%
Test Standard	Enterprise Standard
Consuetudinem	Chiral Compositions;Pharmaceutical intermedia

Sarcina & Repono:

sarcina: Utrem, 25kg/ferrum, vel secundum exigentiam emptoris.

Repono Condition:Repone in vasis signatis in loco frigido et sicco;Protege a lumine, humore et pestis infestatione.

commoda:

FAQ:

Applicatio:

Shanghai Ruifu Chemical Co., Ltd. est primarius fabrica et supplementum (±) - trans-1,2-Diaminocyclohexane (CAS: 1121-22-8) magna qualitate.

(±)-trans 1,2-Diaminocyclohexanum (CAS: 1121-22-8) compositum est organicum cum formula C6H10(NH2)2.Haec diaminea est aedificium scandalum pro ligandis C2-symmetricis quae in catalysi asymmetrica utiles sunt.(±) -trans-1,2-Diaminocyclohexanei adhibetur in synthesi macrocyclicae [3+3] hexai Schiff basis.Etiam magni ponderis munus agit in parandis ligandis multidentatis, auxiliis chiralibus et gradibus chiralibus stationariis.Praeterea, macrocyclizationem adhibendo cum dialdehydibus aliphaticis praeparare solet.Huc accedit, quod ligandum chirale agit, quod applicationem in catalysi asymmetrica invenit.