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重要文件

339938

Sigma-Aldrich

3,4-二氨基甲苯

99%, purified by sublimation

同義詞:

4-甲基--苯二胺, 3,4-甲苯二胺

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About This Item

線性公式:
CH3C6H3(NH2)2
CAS號碼:
分子量::
122.17
Beilstein:
507965
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
暫時無法取得訂價和供貨情況

化驗

99%

純化經由

sublimation

bp

155-156 °C/18 mmHg (lit.)

mp

87-89 °C (lit.)

SMILES 字串

Cc1ccc(N)c(N)c1

InChI

1S/C7H10N2/c1-5-2-3-6(8)7(9)4-5/h2-4H,8-9H2,1H3

InChI 密鑰

DGRGLKZMKWPMOH-UHFFFAOYSA-N

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一般說明

3,4-Diaminotoluene on treatment with [{PhP(Se)(μ-Se)}2], causes the rupture of the dimer, giving PhP(Se)(NHC6H3(CH3-3)NH-1,2).[1]

應用

3,4-Diaminotoluene was employed as catalyst for the two-step reduction of Zn(II) ions at dropping mercury electrode in 1M NaClO4 + 0.001M HClO4.[2] It was also used in the synthesis of new benzimidazole derivatives with cyclohexylalkyl and aralkyl substituents in position 2.[3]

象形圖

Exclamation mark

訊號詞

Warning

危險分類

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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The catalysis of the reduction of Zn (II) ions by 3, 4-diaminotoluene.
Dalmata G.
Electrochimica Acta, 42(9), 1307-1314 (1997)
Bridge cleavage of [{PhP(Se)(?-Se)}2] by 1,2- C6H4(EH)(E'H) (E, E'=O or NH). X-ray crystal structure of PhP(Se)(NHC6H4NH-1,2).
Bhattacharyya P, et al.
Journal of Organometallic Chemistry, 623(1), 116-119 (2001)
Synthesis and tuberculostatic activity of new benzimidazole derivatives.
Foks H, et al.
Chemistry of Heterocyclic Compounds, 42(5), 611-614 (2006)
P J Becci et al.
Toxicology and applied pharmacology, 71(3), 323-329 (1983-12-01)
o-Toluenediamine in corn oil was administered po to Sprague-Dawley rats at dosages of 10, 30, 100, or 300 mg/kg body wt/day during Days 6 through 15 of gestation. All animals were killed on Day 20 of gestation. A similar study
T A Marks et al.
Teratology, 24(3), 253-265 (1981-12-01)
Pregnant outbred albino (CD-1) mice were given 2-nitro-p-phenylenediamine (2NPPD; 32-256 mg/kg/day), 4-nitro-o-phenylenediamine (4NOPD; 16-1024 mg/kg/day) or 2,5-toluenediamine sulfate (2,5TDS; 16-64 mg/kg/day) by subcutaneous injection on Days 6-15 of gestation. The mice were killed on Day 18, the general health and

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